- About this Journal ·
- Abstracting and Indexing ·
- Aims and Scope ·
- Annual Issues ·
- Article Processing Charges ·
- Articles in Press ·
- Author Guidelines ·
- Bibliographic Information ·
- Citations to this Journal ·
- Contact Information ·
- Editorial Board ·
- Editorial Workflow ·
- Free eTOC Alerts ·
- Publication Ethics ·
- Reviewers Acknowledgment ·
- Submit a Manuscript ·
- Subscription Information ·
- Table of Contents
International Journal of Alzheimer's Disease
Volume 2012 (2012), Article ID 578373, 7 pages
Tau Phosphorylation by GSK3 in Different Conditions
1Centro de Biologia Molecular “Severo Ochoa” (CSIC-UAM), Nicolás Cabrera 1, Campus Cantoblanco UAM, 28049 Madrid, Spain
2Centro de Investigación Biomédica en Red de Enfermedades neurodegenerativas (CIBERNED), 28031 Madrid, Spain
3Instituto Cajal, Consejo Superior de Investigaciones Científicas, 28002 Madrid, Spain
4Laboratorio Cajal de Circuitos Corticales, Centro de Tecnología Biomédica, Universidad Politécnica de Madrid, 28223 Madrid, Spain
Received 17 January 2012; Accepted 15 March 2012
Academic Editor: Hanna Rosenmann
Copyright © 2012 Jesús Avila et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Almost a 20% of the residues of tau protein are phosphorylatable amino acids: serine, threonine, and tyrosine. In this paper we comment on the consequences for tau of being a phosphoprotein. We will focus on serine/threonine phosphorylation. It will be discussed that, depending on the modified residue in tau molecule, phosphorylation could be protective, in processes like hibernation, or toxic like in development of those diseases known as tauopathies, which are characterized by an hyperphosphorylation and aggregation of tau.
Tau protein was discovered as one of the brain microtubule-associated proteins bound to in vitro assembled tubulin . Tau protein appears as a series of different polypeptides on gel electrophoresis. These different forms are generated by alternative RNA splicing  or by different phosphorylation levels . In every tau form, four different regions could be identified: the amino terminal region, the proline-rich region, the microtubule binding region, and the carboxy terminal region. Here, we will mainly comment on the tau molecule of the largest tau form present in the central nervous system (CNS) . This molecule contains 441 residues. The N-terminal region (1–150 residues) and the proline-rich region (151–239 residues) have been involved in the interaction of tau protein with cell membranes [5, 6]. The microtubule-binding region (residues 240–367) contains four similar but not identical sequences involved in the interaction with tubulin , the main component of microtubules. The last part of the molecule is the C-terminal region (residues 368 to 441). Curiously, for a specific residue, threonine, there is a decreasing gradient in its presence from the N-terminal to the C-terminal region in human tau. Threonine is particularly abundant at the N-terminal region . Some of these threonines, residues 17, 30, 39, 50, 52, or 95, present in human tau are not always conserved in other species and may have appeared during evolution in human tau. None of these human tau threonines have been found to be phosphorylated, but we cannot rule out that some of these sites could be modified with a very fast turnover.
2. Tau Functions
Tau is a neuronal microtubule-associated protein, and some of its functions are related to that association that may result in microtubule stabilization or the regulation of axonal transport, but tau protein is a “sticky” protein that could bind to other proteins, apart from tubulin (the main component of microtubules), which could also facilitate its subcellular localization at the cytoplasm close to the membrane or in the nucleus. On the other hand, in the neuron, tau is mainly present in axons, owing to a sorting mechanism in which its level of phosphorylation may play a role , but tau can be also localized, at a low level, to dendrites  where it binds to PSD95 protein, a postsynaptic component present in dendritic spines, which is bound to glutamate (NMDA) receptors .
Some of tau functions could be regulated by phosphorylation. In many cases, tau phosphorylation can cause its detachment from microtubules , and those functions like microtubule stabilization and regulation of axonal transport could be affected by the change in the association of tau to microtubules.
Tau is a phosphoprotein that could be modified by different protein kinases at tyrosine, threonine, or serine residues. In the longest CNS tau molecule, there are 80 serine/threonine residues that are mainly present at the proline-rich and C-terminal regions .
Tau kinases have been divided in proline- (PDPK) and nonproline- (NPDPK) directed protein kinases, being GSK3 the PDPK that could modify more sites in tau molecule . These sites are also mainly present at the proline-rich and C-terminal regions.
GSK3 is a protein kinase originally identified due to its role in glycogen metabolism regulation. GSK3, one of its isoforms, is abundant in the central nervous system and can modify several neuronal proteins like tau .
Tau hyperphosphorylation takes place, at the CNS, in several diseases (tauopathies), being the most predominant of these disorders, Alzheimer disease. In the tauopathies, tau protein is not only phosphorylated but also could be found in aggregated form. In Alzheimer’s disease (AD) tau protein can be assembled into the paired helical filaments that form the aberrant structure known as neurofibrillary tangles . Also, in AD, there is another aberrant structure the senile plaques, composed by the beta-amyloid peptide. A relationship between NFT and SP has been suggested through GSK3 (see below and ).
4. GSK3 and AD
In Alzheimer’s disease postmortem brain material, tau phosphorylation has been found to increase at several sites modified by GSK3. In this way, the analysis of how an increase in GSK3 activity could modify tau protein has been deeply studied. It is known the involvement of factors like wnt, insulin, or insulin-like growth factor in the regulation of GSK3 . It is also known that the accumulation of beta-amyloid peptide facilitates tau phosphorylation by GSK3 through the interference with insulin or wnt pathways [16, 17]. Also, mutations in the protein presenilin-1 (PS-1) that could result in the appearance of dementia with familiar origin may affect the interaction of PS-1 with the regulatory subunit of PI3 kinase, decreasing the activity of this kinase and the further activation of GSK3 . On the other hand, in nonfamilial dementia like sporadic Alzheimer disease, the presence of apolipoprotein E4 isoform could facilitate a higher GSK3 activity . Also, a GSK3 polymorphism has been associated with Alzheimer’s disease , and an increase in GSK3 activity has been suggested to take place in the brain of AD patients . Finally, GSK3 phosphorylates the majority of sites, on tau molecule, which are abnormally phosphorylated in AD .
One of the consequences of tau phosphorylation by GSK3 is a decrease of its interaction with microtubules , which could result in a destabilization of microtubule network . Also, phosphorylation of tau by GSK3 (or other kinases) may result in an increase or a decrease in its interaction with other proteins. An increase was observed in its interaction with prolyl isomerase 1 (PIN-1), a chaperone protein that binds to phosphotau . In this interaction phosphothreonine 231 is involved. On the other hand, Pin-1 could inhibit GSK3, and a consequence of that is a reduced phosphorylation of amyloid precursor protein (APP), another important protein in AD. In the absence of phosphorylation, the turnover of APP is increased . Also, Pin-1 acts on T668P motif in APP to promote non-amyloidogenic APP processing . About GSK3 and APP processing it should be indicated a report indicating that GSK3, mainly GSK3, can regulate APP processing and the production of amyloid beta peptide .
Going back to tau phosphorylation, it has been observed that the interaction of tau with cell membranes decreases upon its phosphorylation . In this binding, phosphorylation of serine 202 may play a role. Thus, the balance of kinase and phosphatases acting on tau could be important for tau functions and dysfunctions.
5. Is Phosphotau Toxic or Protective in a Neuron?
Since tau phosphorylation may affect tau functions, it was suggested that phosphotau could be toxic. However, this point has been widely discussed and is commented if phosphorylated tau is toxic, protective, or none of the above .
Working on Drosophila as a model it was indicated that phosphotau is not toxic [29, 30]. Also, there are some works suggesting that tau toxicity could be dependent in an increase in its expression  or that the toxicity could be related to its fragmentation, yielding some specific peptides , or to its aggregation, but this point is also discussed, since some works suggest a protective role for large tau aggregates, although it may be insufficient in damaged neurons [33, 34]. More recently, it has been suggested a toxicity for tau oligomers . A possible relation between tau phosphorylation and aggregation has been suggested. In a mouse model for temporal dementia, chronic lithium (a GSK3 inhibitor) treatment results in a decreased tau phosphorylation and aggregation . In another study a similar result was found , being the site recognized by antibody PHF-1 one of the phosphosites with a higher decrease upon treatment with a GSK3 inhibitor. It may suggest that tau phosphorylation at some sites may facilitate tau aggregation. These results support the previous works indicating that large tau aggregates exert negligible neurotoxicity compared with soluble tau [38, 39].
A protective role for tau phosphorylation could be suggested when that modification could take place at threonine 181  that could facilitate its binding to exosomes and the release of tau excess . Also phosphorylation at serine 202 could prevent the tau proteolysis by calpain , or in some processes, like hibernation (see below), it could be also protective . Although poorly understood, there is an endocrine regulation of hibernation, and a recent study suggests that central system neurons are protected from low-temperature cell death by certain endogenous substances such as adenosine, opioids, and histamine .
On the other hand, tau toxicity resulting from tau phosphorylation could affect to axonal transport, mitochondrial respiration, or cytoskeletal changes [45, 46]. Also, the presence of hyperphosphorylated tau in dendritic spines impairs synaptic activity , and tau phosphorylation by GSK3 in the hippocampus results in a toxic gain of function [48, 49].
A way to study the role of tau phosphorylation on cell toxicity is the use of pseudophosphorylated tau variants where a serine or threonine residue is replaced by glutamatic acid. Thus, it has been found that pseudophosphorylation at the site recognized by antibody AT8, but not at the site recognized by abPHF-1, prevents the interaction of tau with neuronal membranes [50, 51].
Pseudophosphorylation of tau in ten different sites of a single molecule (including those sites recognized by AT8, ab PHF-1, and phosphothreonine 231) results in a toxic action and the induction of apoptosis .
Combined pseudophosphorylation at threonine 212, threonine 231, and serine 262 causes neurodegeneration, mainly through the presence of pseudophosphorylation at threonine 212 . A possible mechanism has been involved for this toxicity: abnormal tau phosphorylation can result in the sequestration of unmodified tau  or in that of other microtubule associated proteins like MAP1 or MAP2 , promoting a net microtubule disassembly that could affect neuron cytoskeleton and promote neurodegeneration. On the other hand, tau phosphorylated at Thr 231 is used as a marker for neurodegeneration. It may suggest that tau modified at that residue could be toxic .
All those results suggest that, depending on the modified site, a protective or toxic function may take place and that it could be due to different conformational changes of tau molecule. Although tau is an unstructured molecule, it has been suggested that, in some conditions, it could have a paperclip conformation. In this conformation, the C-terminal end of tau interacts with the microtubule-binding domain, whereas the N-terminal end could bind to the C-terminal region, adopting a paperclip folding . Pseudophosphorylation at the AT8 site makes the N-terminal region away from the C-terminal. On the other hand, pseudophosphorylation at the PHF-1 site decreases the interaction of C-terminal region with microtubule binding domain . Thus, phosphorylation at different sites of tau molecule could have different consequences for tau conformations and function. In this way, we will comment more on the phosphorylation of tau on those sites recognized by ab AT8 or ab PHF-1.
6. The Progression of Alzheimer and the Phosphorylation of Tau by GSK3 at Two Different Sites
At the level of degeneration of a single neuron, occurring in Alzheimer’s disease, it was suggested that first takes place phosphorylation of tau molecule at some specific sites and afterwards there is a further phosphorylation and aggregation of tau protein. Thus, early tau phosphorylation can be used as an initial marker for neurodegeneration .
The phosphorylation of tau, by GSK3, at specific sites can be analyzed by the use of antibodies that specifically recognize some of those sites. In this way, analysis of phosphorylation at serine 202 or at serines 396–404 could be achieved by using the antibodies AT8  or PHF-1 , respectively. The uses of these antibodies have indicated that different tau molecules could be modified at those different sites . On the other hand, in mature neurons tau phosphorylated at the site recognized by PHF-1 is preferentially present in the axon, whereas tau modified at AT8 site is located in the somatodendritic compartment . Temporal lobe sections, including the entorhinal region and hippocampus, were studied using the antibody AT8 in AD patients and controls, to follow the consequences of that phosphorylation at the level of a single neuron and its possible relation with tau aggregation. The analysis showed that tau was modified at the site recognized by ab AT8 much earlier than the appearance of aggregated (fibrillar) tau, suggesting that phosphorylation at the AT8 site represents an earlier change than tau aggregation . More recently, by looking at specific neurons in the brain of Alzheimer’s disease patients like those present in the CA3 region of the hippocampus, the sequence for cellular changes related to tau phosphorylation and the posterior formation of aggregates has been studied with tau antibody AT8. This antibody recognizes the first stages of tau phosphorylation (pretangle stages) , whereas the reaction with tau antibody PHF-1 could correlate further phosphorylation steps and the formation of tau aggregates (tangle stages) .
Tau phosphorylation (recognized by AT8 antibody) at regions like CA3 of the hippocampus has been correlated with regression of synaptic components and memory deficits . Indeed, although in AD there is neuron death, it has been suggested that there also could be alive neurons undergoing atrophy . This atrophy could be the consequence of a metabolic decline  (that could be a very early sign of AD). Indeed, there is a reduced metabolism in those regions of the brain that are later affected in AD patients, and this glucose hypometabolism may reflect a reduced synaptic activity. This reduced metabolism may induce hypothermia, decreasing the activity of phosphatases that could result in the net phosphorylation of GSK3 substrates like tau protein .
A main difference between neuron atrophy and neuron death is that in the first case the neuron remains alive and could be possible to reactivate it. In fact, we have recently observed that in patients with AD the accumulation of phosphotau in a pretangle state does not induce changes in the dendrites of pyramidal neurons, whereas the presence of tau aggregates forming intraneuronal neurofibrillary tangles gives rise to a progressive dendritic atrophy and the loss of dendritic spines (synaptic disconnection) (Merino-Serrais P et al. in preparation). Thus, the presence of phosphotau in a pretangle state in neurons of the human brain does not necessarily result in severe and irreversible effects. Thus, it is of great interest to search for possible physiological conditions in which neurons with a reduced metabolism and altered synaptic connectivity that may result in the lack of cognitive functions could be reactivated to regular functionally neurons. The group of Arendt et al.  answers to that question by showing that topor in hibernating animals shows a significant analogy with the pretangle stages of AD. Hibernation is a behavioral strategy used by some mammals to minimize energy expenditure under inhospitable environmental conditions. During hibernation overall metabolic rates are greatly reduced and neurons like those of the CA3 hippocampal regions have a reduced metabolism . Moreover, tau phosphorylation also takes place in those neurons, at sites recognized by AT8 antibody, phosphorylation which is fully reversed in a few hours when these animals spontaneously interrupt torpor by an arousal leading the animals to euthermia for 24 h approximately . Furthermore, it has been shown that there is a re-establishment of mossy fiber synapses in CA3 neurons after arousal . Previous studies have shown that neuronal cell bodies, dendrites, and spines in hibernating ground squirrels retract on entry into torpor state. When they return to euthermia, there is a recovery of the arbor complexity and spine density .
Thus, if topor stage, in hibernation, is similar to the pretangle stages in AD and it could be reversed, we could ask if that reversion could also take place in AD. This question has pros and cons. One of the cons is that the primary structure of tau from hibernating animals could be different than that of a human being. Thus, tau from hibernating mammals have been sequenced , but no dramatic differences with human tau were found. Then, how can we increase metabolic rate in AD neurons? In a further analysis, tau protein from Mesocricetus auratus (another hibernating rodent) has been sequenced and characterized (Leon G et al. in preparation). The reason of that characterization has been to perform a first step to know if tau protein in hibernating animals, like M. auratus, could be taken as a single marker of the process or it may play a role in it. Thus, tau differences between this hibernating animal and nonhibernating organisms like the human being should be carried out. Our results have indicated the presence of several variations at the N-terminal half between M. auratus and human tau. Some of these variations have been also found in nonhibernating rodents. However, there are three variations, in that region, which are only present in the two hibernating rodents, M. auratus and S. citellus. In addition, there are another differences between M. auratus and human tau like the presence of 10 phosphorylatable residues present in human but not in M. auratus tau (Leon G et al. in preparation). Many of these phosphorylatable residues could be possible substrates for ck1, a protein kinase that has been related with circadian rhythm in nonhibernating organism [72, 73]. Although additional work should be done, our observations are compatible with a possible role of tau in the hibernation process and not being only found as a single marker.
It could be a possible relationship between hibernation/wake in hibernating mammals and sleep/wake in humans. Indeed, AD patients exhibit sleep/wake disorders . However, sleep deprivation has been associated with GSK3 activation , whereas a net GSK3 phosphorylation takes place in hibernating mammals . Nevertheless, modulators of sleep/wake cycle, like melatonin, have been suggested as possible therapeutical compounds for AD .
A more related behavior to that of hibernation could be anesthesia. Anesthesia leads to tau hyperphosphorylation through inhibition of phosphatase activity by hypothermia , a process that could be similar to that of hibernation. However, little is known about how is the recovery from phosphotau to unmodified tau after anesthesia. In addition, we do not know if tau phosphorylation is sometimes associated with the physiological conditions following hibernation or anesthesia or, like in AD, may play a toxic function . Thus, if phosphotau could be toxic and it is difficult to active phosphatases for its dephosphorylation, the use of possible GSK3 inhibitors should be taken into consideration for the treatment of the disease.
Furthermore, we should look for better analysis to detect a decreased metabolic rate in damaged CA3 neurons in AD, and we should look for an answer about how to increase that metabolic rate in AD neurons. A probable common link among some of these disorders is the appearance of oxidative damage that results in neurodegeneration [79, 80].
A possible mechanism has been suggested to explain an energy depletion in AD. It involves that oxidative stress may lead to the formation of reactive carbonyl compounds  that appear to increase in AD patients. These compounds may decrease glucose metabolism yielding to energy depletion in neuronal cells . Also, intracellular A may cause mitochondrial defects and ATP depletion.
In summary, since neuron atrophy in neurodegenerative diseases, like AD, has been correlated with tau phosphorylation by GSK3, it should be tested in the future if by decreasing that phosphorylation that atrophy could be reversed or not.
- M. D. Weingarten, A. H. Lockwood, S. Y. Hwo, and M. W. Kirschner, “A protein factor essential for microtubule assembly,” Proceedings of the National Academy of Sciences of the United States of America, vol. 72, no. 5, pp. 1858–1862, 1975.
- A. Himmler, D. Drechsel, M. W. Kirschner, and D. W. Martin, “Tau consists of a set of proteins with repeated C-terminal microtubule-binding domains and variable N-terminal domains,” Molecular and Cellular Biology, vol. 9, no. 4, pp. 1381–1388, 1989.
- J. G. De Ancos, I. Correas, and J. Avila, “Differences in microtubule binding and self-association abilities of bovine brain tau isoforms,” Journal of Biological Chemistry, vol. 268, no. 11, pp. 7976–7982, 1993.
- M. Goedert, M. G. Spillantini, M. C. Potier, J. Ulrich, and R. A. Crowther, “Cloning and sequencing of the cDNA encoding an isoform of microtubule-associated protein tau containing four tandem repeats: differential expression of tau protein mRNAs in human brain,” The EMBO Journal, vol. 8, no. 2, pp. 393–399, 1989.
- R. Brandt, J. Léger, and G. Lee, “Interaction of tau with the neural plasma membrane mediated by tau's amino-terminal projection domain,” Journal of Cell Biology, vol. 131, no. 5, pp. 1327–1340, 1995.
- M. Arrasate, M. Pérez, and J. Avila, “Tau dephosphorylation at Tau-1 site correlates with its association to cell membrane,” Neurochemical Research, vol. 25, no. 1, pp. 43–50, 2000.
- G. Lee, N. Cowan, and M. Kirschner, “The primary structure and heterogeneity of tau protein from mouse brain,” Science, vol. 239, no. 4837, pp. 285–288, 1988.
- X. Li, Y. Kumar, H. Zempel, E. M. Mandelkow, J. Biernat, and E. Mandelkow, “Novel diffusion barrier for axonal retention of Tau in neurons and its failure in neurodegeneration,” The EMBO Journal, vol. 30, pp. 4825–4837, 2011.
- L. M. Ittner, Y. D. Ke, F. Delerue et al., “Dendritic function of tau mediates amyloid-β toxicity in alzheimer's disease mouse models,” Cell, vol. 142, no. 3, pp. 387–397, 2010.
- M. W. Salter and L. V. Kalia, “SRC kinases: a hub for NMDA receptor regulation,” Nature Reviews Neuroscience, vol. 5, no. 4, pp. 317–328, 2004.
- J. Avila, J. J. Lucas, M. Perez, and F. Hernandez, “Role of tau protein in both physiological and pathological conditions,” Physiological Reviews, vol. 84, pp. 361–384, 2004.
- D. P. Hanger, B. H. Anderton, and W. Noble, “Tau phosphorylation: the therapeutic challenge for neurodegenerative disease,” Trends in Molecular Medicine, vol. 15, no. 3, pp. 112–119, 2009.
- S. Frame and P. Cohen, “GSK3 takes centre stage more than 20 years after its discovery,” Biochemical Journal, vol. 359, no. 1, pp. 1–16, 2001.
- F. Hernandez, E. Gomez de Barreda, A. Fuster-Matanzo, J. J. Lucas, and J. Avila, “GSK3: a possible link between beta amyloid peptide and tau protein,” Experimental Neurology, vol. 223, pp. 322–325, 2010.
- F. Hernández, E. G. D. Barreda, A. Fuster-Matanzo, P. Goñi-Oliver, J. J. Lucas, and J. Avila, “The role of GSK3 in Alzheimer disease,” Brain Research Bulletin, vol. 80, no. 4-5, pp. 248–250, 2009.
- M. H. Magdesian, M. M. V. F. Carvalho, F. A. Mendes et al., “Amyloid-β binds to the extracellular cysteine-rich domain of frizzled and inhibits Wnt/β-catenin signaling,” Journal of Biological Chemistry, vol. 283, no. 14, pp. 9359–9368, 2008.
- M. Townsend, T. Mehta, and D. J. Selkoe, “Soluble Aβ inhibits specific signal transduction cascades common to the insulin receptor pathway,” Journal of Biological Chemistry, vol. 282, no. 46, pp. 33305–33312, 2007.
- L. Baki, J. Shioi, P. Wen et al., “PS1 activates PI3K thus inhibiting GSK-3 activity and tau overphosphorylation: effects of FAD mutations,” The EMBO Journal, vol. 23, no. 13, pp. 2586–2596, 2004.
- A. Cedazo-Mínguez, B. O. Popescu, J. M. Blanco-Millán et al., “Apolipoprotein E and β-amyloid (1-42) regulation of glycogen synthase kinase-3β,” Journal of Neurochemistry, vol. 87, no. 5, pp. 1152–1164, 2003.
- B. A. J. Schaffer, L. Bertram, B. L. Miller et al., “Association of GSK3B with Alzheimer disease and frontotemporal dementia,” Archives of Neurology, vol. 65, no. 10, pp. 1368–1374, 2008.
- J. J. Pei, E. Braak, H. Braak et al., “Distribution of active glycogen synthase kinase 3beta (GSK-3beta) in brains staged for Alzheimer disease neurofibrillary changes,” Journal of Neuropathology & Experimental Neurology, vol. 58, pp. 1010–1019, 1999.
- U. Wagner, M. Utton, J. M. Gallo, and C. C. J. Miller, “Cellular phosphorylation of tau by GSK-3β influences tau binding to microtubules and microtubule organisation,” Journal of Cell Science, vol. 109, no. 6, pp. 1537–1543, 1996.
- A. D. C. Alonso, I. Grundke-Iqbal, H. S. Barra, and K. Iqbal, “Abnormal phosphorylation of tau and the mechanism of Alzheimer neurofibrillary degeneration: sequestration of microtubule-associated proteins 1 and 2 and the disassembly of microtubules by the abnormal tau,” Proceedings of the National Academy of Sciences of the United States of America, vol. 94, no. 1, pp. 298–303, 1997.
- P. J. Lu, G. Wulf, X. Z. Zhou, P. Davies, and K. P. Lu, “The prolyl isomerase Pin1 restores the function of Alzheimer-associated phosphorylated tau protein,” Nature, vol. 399, no. 6738, pp. 784–788, 1999.
- S. L. Ma, L. Pastorino, X. Z. Zhou, and K. P. Lu, “Prolyl isomerase Pin1 promotes amyloid precursor protein (APP) turnover by inhibiting glycogen synthase kinase-3beta (GSK3beta) activity: novel mechanism for Pin1 to protect against alzheimer disease,” The Journal of Biological Chemistry, vol. 287, pp. 6969–6973, 2012.
- L. Pastorino, A. Sun, P. J. Lu et al., “The prolyl isomerase Pin1 regulates amyloid precursor protein processing and amyloid-β production,” Nature, vol. 440, no. 7083, pp. 528–534, 2006.
- C. J. Phiel, C. A. Wilson, V. M. Y. Lee, and P. S. Klein, “GSK-3α regulates production of Alzheimer's disease amyloid-β peptides,” Nature, vol. 423, no. 6938, pp. 435–439, 2003.
- R. J. Castellani, A. Nunomura, H. G. Lee, G. Perry, and M. A. Smith, “Phosphorylated tau: toxic, protective, or none of the above,” Journal of Alzheimer's Disease, vol. 14, no. 4, pp. 377–383, 2008.
- S. Chatterjee, T. K. Sang, G. M. Lawless, and G. R. Jackson, “Dissociation of tau toxicity and phosphorylation: role of GSK-3β, MARK and Cdk5 in a Drosophila model,” Human Molecular Genetics, vol. 18, no. 1, pp. 164–177, 2009.
- Y. Talmat-Amar, Y. Arribat, C. Redt-Clouet et al., “Important neuronal toxicity of microtubule-bound Tau in vivo in Drosophila,” Human Molecular Genetics, vol. 20, pp. 3738–3745, 2011.
- C. Andorfer, C. M. Acker, Y. Kress, P. R. Hof, K. Duff, and P. Davies, “Cell-cycle reentry and cell death in transgenic mice expressing nonmutant human tau isoforms,” Journal of Neuroscience, vol. 25, no. 22, pp. 5446–5454, 2005.
- J. Reifert, D. Hartung-Cranston, and S. C. Feinstein, “Amyloid β-mediated cell death of cultured hippocampal neurons reveals extensive Tau fragmentation without increased full-length Tau phosphorylation,” Journal of Biological Chemistry, vol. 286, no. 23, pp. 20797–20811, 2011.
- L. Aarden, S. R. Ruuls, and G. Wolbink, “Immunogenicity of anti-tumor necrosis factor antibodies-toward improved methods of anti-antibody measurement,” Current Opinion in Immunology, vol. 20, no. 4, pp. 431–435, 2008.
- F. Hernández and J. Avila, “Tau aggregates and tau pathology,” Journal of Alzheimer's Disease, vol. 14, no. 4, pp. 449–452, 2008.
- C. A. Lasagna-Reeves, D. L. Castillo-Carranza, M. J. Guerrero-Muñoz, G. R. Jackson, and R. Kayed, “Preparation and characterization of neurotoxic tau oligomers,” Biochemistry, vol. 49, no. 47, pp. 10039–10041, 2010.
- M. Perez, F. Hernandez, F. Lim, J. Diaz-Nido, and J. Avila, “Chronic lithium treatment decreases mutant tau protein aggregation in a transgenic mouse model,” Journal of Alzheimer's Disease, vol. 5, pp. 301–308, 2003.
- W. Noble, E. Planel, C. Zehr et al., “Inhibition of glycogen synthase kinase-3 by lithium correlates with reduced tauopathy and degeneration in vivo,” Proceedings of the National Academy of Sciences of the United States of America, vol. 102, no. 19, pp. 6990–6995, 2005.
- S. Oddo, V. Vasilevko, A. Caccamo, M. Kitazawa, D. H. Cribbs, and F. M. LaFerla, “Reduction of soluble Aβ and tau, but not soluble Aβ alone, ameliorates cognitive decline in transgenic mice with plaques and tangles,” Journal of Biological Chemistry, vol. 281, no. 51, pp. 39413–39423, 2006.
- K. Santacruz, J. Lewis, T. Spires et al., “Medicine: Tau suppression in a neurodegenerative mouse model improves memory function,” Science, vol. 309, no. 5733, pp. 476–481, 2005.
- S. Saman, W. Kim, M. Raya, et al., “Exosome-associated tau is secreted in tauopathy models and is selectively phosphorylated in cerebrospinal fluid (CSF) in early Alzheimer's Disease,” The Journal of Biological Chemistry, vol. 287, no. 6, pp. 3842–3849, 2012.
- D. Simon, E. Garcia-Garcia, F. Royo, J. M. Falcon-Perez, and J. Avila, “Proteostasis of tau. Tau overexpression results in its secretion via membrane vesicles,” The FEBS Letter, vol. 586, pp. 47–54, 2012.
- G. V. W. Johnson, R. S. Jope, and L. I. Binder, “Proteolysis of tau by calpain,” Biochemical and Biophysical Research Communications, vol. 163, no. 3, pp. 1505–1511, 1989.
- F. Zhou, X. Zhu, R. J. Castellani et al., “Hibernation, a model of neuroprotection,” American Journal of Pathology, vol. 158, no. 6, pp. 2145–2151, 2001.
- Y. Tamura, M. Monden, M. Shintani, A. Kawai, and H. Shiomi, “Neuroprotective effects of hibernation-regulating substances against low-temperature-induced cell death in cultured hamster hippocampal neurons,” Brain Research, vol. 1108, no. 1, pp. 107–116, 2006.
- A. Ittner, Y. D. Ke, J. Van Eersel, A. Gladbach, J. Götz, and L. M. Ittner, “Brief update on different roles of tau in neurodegeneration,” IUBMB Life, vol. 63, no. 7, pp. 495–502, 2011.
- H. Moreno, S. Choi, E. Yu et al., “Blocking effects of human Tau on squid giant synapse transmission and its prevention by T-817 MA,” Frontiers in Synaptic Neuroscience, vol. 3, article 3, 2011.
- B. R. Hoover, M. N. Reed, J. Su et al., “Tau mislocalization to dendritic spines mediates synaptic dysfunction independently of neurodegeneration,” Neuron, vol. 68, no. 6, pp. 1067–1081, 2010.
- J. Avila, E. Gómez De Barreda, T. Engel, J. J. Lucas, and F. Hernández, “Tau phosphorylation in hippocampus results in toxic gain-of-function,” Biochemical Society Transactions, vol. 38, no. 4, pp. 977–980, 2010.
- E. G. de Barreda, M. Pérez, P. G. Ramos et al., “Tau-knockout mice show reduced GSK3-induced hippocampal degeneration and learning deficits,” Neurobiology of Disease, vol. 37, no. 3, pp. 622–629, 2010.
- A. M. Pooler and D. P. Hanger, “Functional implications of the association of tau with the plasma membrane,” Biochemical Society Transactions, vol. 38, no. 4, pp. 1012–1015, 2010.
- A. M. Pooler, A. Usardi, C. J. Evans, K. L. Philpott, W. Noble, and D. P. Hanger, “Dynamic association of tau with neuronal membranes is regulated by phosphorylation,” Neurobiology of Aging, vol. 33, no. 2, pp. 431.e27–431.e38, 2012.
- T. Fath, J. Eidenmüller, and R. Brandt, “Tau-mediated cytotoxicity in a pseudohyperphosphorylation model of Alzheimer's disease,” Journal of Neuroscience, vol. 22, no. 22, pp. 9733–9741, 2002.
- A. D. Alonso, J. Di Clerico, B. Li et al., “Phosphorylation of Tau at Thr212, Thr231, and Ser262 combined causes neurodegeneration,” Journal of Biological Chemistry, vol. 285, no. 40, pp. 30851–30860, 2010.
- A. Del, I. Grundke-Iqbal, and K. Iqbal, “Alzheimer's disease hyperphosphorylated tau sequesters normal tau into tangles of filaments and disassembles microtubules,” Nature Medicine, vol. 2, no. 7, pp. 783–787, 1996.
- L. Glodzik, Santi S. de, W. H. Tsui, et al., “Phosphorylated tau 231, memory decline and medial temporal atrophy in normal elders,” Neurobiology of Aging, vol. 32, pp. 2131–2141, 2011.
- S. Jeganathan, M. Von Bergen, H. Brutlach, H. J. Steinhoff, and E. Mandelkow, “Global hairpin folding of tau in solution,” Biochemistry, vol. 45, no. 7, pp. 2283–2293, 2006.
- S. Jeganathan, A. Hascher, S. Chinnathambi, J. Biernat, E. M. Mandelkow, and E. Mandelkow, “Proline-directed pseudo-phosphorylation at AT8 and PHF1 epitopes induces a compaction of the paperclip folding of tau and generates a pathological (MC-1) conformation,” Journal of Biological Chemistry, vol. 283, no. 46, pp. 32066–32076, 2008.
- E. Braak, H. Braaak, and E. M. Mandelkow, “A sequence of cytoskeleton changes related to the formation of neurofibrillary tangles and neuropil threads,” Acta Neuropathologica, vol. 87, no. 6, pp. 554–567, 1994.
- M. Mercken, M. Vandermeeren, U. Lubke et al., “Monoclonal antibodies with selective specificity for Alzheimer Tau are directed against phosphatase-sensitive epitopes,” Acta Neuropathologica, vol. 84, no. 3, pp. 265–272, 1992.
- L. Otvos Jr., L. Feiner, E. Lang, G. I. Szendrei, M. Goedert, and V. M. Y. Lee, “Monoclonal antibody PHF-1 recognizes tau protein phosphorylated at serine residues 396 and 404,” Journal of Neuroscience Research, vol. 39, no. 6, pp. 669–673, 1994.
- F. Hernández, J. J. Lucas, R. Cuadros, and J. Avila, “GSK-3 dependent phosphoepitopes recognized by PHF-1 and AT-8 antibodies are present in different tau isoforms,” Neurobiology of Aging, vol. 24, no. 8, pp. 1087–1094, 2003.
- A. Delacourte, J. P. David, N. Sergeant et al., “The biochemical pathway of neurofibrillary degeneration in aging and Alzheimer's disease,” Neurology, vol. 52, no. 6, pp. 1158–1165, 1999.
- L. Blazquez-Llorca, V. Garcia-Marin, P. Merino-Serrais, J. Avila, and J. Defelipe, “Abnormal Tau phosphorylation in the thorny excrescences of CA3 hippocampal neurons in patients with Alzheimer's disease,” Journal of Alzheimer's Disease, vol. 26, pp. 683–698, 2011.
- N. Spruston, “Pyramidal neurons: dendritic structure and synaptic integration,” Nature Reviews Neuroscience, vol. 9, no. 3, pp. 206–221, 2008.
- D. F. Swaab, E. J. G. Dubelaar, M. A. Hofman, E. J. A. Scherder, E. J. W. Van Someren, and R. W. H. Verwer, “Brain aging and Alzheimer's disease; use it or lose it,” Progress in Brain Research, vol. 138, pp. 343–373, 2002.
- E. Planel, T. Miyasaka, T. Launey et al., “Alterations in glucose metabolism induce hypothermia leading to Tau hyperphosphorylation through differential inhibition of kinase and phosphatase activities: implications for Alzheimer's disease,” Journal of Neuroscience, vol. 24, no. 10, pp. 2401–2411, 2004.
- T. Arendt, J. Stieler, A. M. Strijkstra et al., “Reversible paired helical filament-like phosphorylation of tau is an adaptive process associated with neuronal plasticity in hibernating animals,” Journal of Neuroscience, vol. 23, no. 18, pp. 6972–6981, 2003.
- W. Härtig, J. Stieler, A. S. Boerema et al., “Hibernation model of tau phosphorylation in hamsters: selective vulnerability of cholinergic basal forebrain neurons—implications for Alzheimer's disease,” European Journal of Neuroscience, vol. 25, no. 1, pp. 69–80, 2007.
- M. Oklejewicz, S. Daan, and A. M. Strijkstra, “Temporal organisation of hibernation in wild-type and tau mutant Syrian hamsters,” Journal of Comparative Physiology, vol. 171, no. 5, pp. 431–439, 2001.
- W. Härtig, M. Oklejewicz, A. M. Strijkstra, A. S. Boerema, J. Stieler, and T. Arendt, “Phosphorylation of the tau protein sequence 199-205 in the hippocampal CA3 region of Syrian hamsters in adulthood and during aging,” Brain Research, vol. 1056, no. 1, pp. 100–104, 2005.
- C. G. Von Der Ohe, C. Darian-Smith, C. C. Garner, and H. C. Heller, “Ubiquitous and temperature-dependent neural plasticity in hibernators,” Journal of Neuroscience, vol. 26, no. 41, pp. 10590–10598, 2006.
- A. S. I. Loudon, Q. J. Meng, E. S. Maywood, D. A. Bechtold, R. P. Boot-Handford, and M. H. Hastings, “The biology of the circadian CK1ε tau mutation in mice and Syrian hamsters: a tale of two species,” Cold Spring Harbor Symposia on Quantitative Biology, vol. 72, pp. 261–271, 2007.
- Q. J. Meng, E. S. Maywood, D. A. Bechtold et al., “Entrainment of disrupted circadian behavior through inhibition of casein kinase 1 (CK1) enzymes,” Proceedings of the National Academy of Sciences of the United States of America, vol. 107, no. 34, pp. 15240–15245, 2010.
- M. Fotuhi, V. Hachinski, and P. J. Whitehouse, “Changing perspectives regarding late-life dementia,” Nature Reviews Neurology, vol. 5, no. 12, pp. 649–658, 2009.
- F. Benedetti, A. Serretti, C. Colombo, C. Lorenzi, V. Tubazio, and E. Smeraldi, “A glycogen synthase kinase 3-β promoter gene single nucleotide polymorphism is associated with age at onset and response to total sleep deprivation in bipolar depression,” Neuroscience Letters, vol. 368, no. 2, pp. 123–126, 2004.
- B. Su, X. Wang, K. L. Drew, G. Perry, M. A. Smith, and X. Zhu, “Physiological regulation of tau phosphorylation during hibernation,” Journal of Neurochemistry, vol. 105, no. 6, pp. 2098–2108, 2008.
- V. Srinivasan, D. W. Spence, S. R. Pandi-Perumal, G. M. Brown, and D. P. Cardinali, “Melatonin in mitochondrial dysfunction and related disorders,” International Journal of Alzheimer's Disease, vol. 2011, Article ID 326320, 16 pages, 2011.
- E. Planel, K. E. G. Richter, C. E. Nolan et al., “Anesthesia leads to tau hyperphosphorylation through inhibition of phosphatase activity by hypothermia,” Journal of Neuroscience, vol. 27, no. 12, pp. 3090–3097, 2007.
- M. T. Lin and M. F. Beal, “Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases,” Nature, vol. 443, no. 7113, pp. 787–795, 2006.
- J. Avila, “Common mechanisms in neurodegeneration,” Nature Medicine, vol. 16, no. 12, p. 1372, 2010.
- M. D. Ledesma, P. Bonay, C. Colaco, and J. Avila, “Analysis of microtubule-associated protein tau glycation in paired helical filaments,” Journal of Biological Chemistry, vol. 269, no. 34, pp. 21614–21619, 1994.
- S. G. de Arriba, G. Stuchbury, J. Yarin, J. Burnell, C. Loske, and G. Münch, “Methylglyoxal impairs glucose metabolism and leads to energy depletion in neuronal cells-protection by carbonyl scavengers,” Neurobiology of Aging, vol. 28, no. 7, pp. 1044–1050, 2007.