Abstract
Starting as a model for developmental genetics, embryology, and organogenesis, the zebrafish has become increasingly popular as a model organism for numerous areas of biology and biomedicine over the last decades. Within haematology, this includes studies on blood cell development and function and the intricate regulatory mechanisms within vertebrate immunity. Here, we review recent studies on the immediate mechanisms mounting an inflammatory response by in vivo analyses using the zebrafish. These recently revealed novel roles of the reactive oxygen species hydrogen peroxide that have changed our view on the initiation of a granulocytic inflammatory response.
1. Introduction
The innate immune system comprises the cells and mechanisms that defend the host from infection by other organisms or damage to tissue integrity, in a nonspecific manner. This means that the cells of the innate system recognise and respond to pathogens and trauma in a generic way, but unlike the adaptive immune system, it does not confer long-lasting or protective immunity to the host. The innate immune system provides an immediate defence. A typical vertebrate immune response depends on the orchestrated motility and activity of various haematopoietic compartments and their interactions that ultimately control the magnitude of the response [1–3]. Inflammation is one of the first responses of the immune system to infection or irritation. Stimulated by factors released from injured cells, it serves to establish a physical barrier against the spread of infection. This further promotes healing of any damaged tissue following the clearance of pathogens or cell debris. Molecules produced during inflammation sensitise pain receptors, cause localised vasodilatation of blood vessels, and attract phagocytes, especially neutrophils and macrophages, which then trigger other parts of the immune system.
Failure to initiate a response allows uncontrolled proliferation of invading microorganisms and severe tissue damage that may become fatal. Failure to resolve an immune response can also cause severe tissue damage, due to persistent degranulation, and may lead to chronic inflammation, which ceases to be beneficial to the host. Overall, inflammation is now recognised as a central feature of prevalent pathologies, such as atherosclerosis, cancer, asthma, thyroiditis, inflammatory bowel disease, autoimmune disease, as well as Alzheimer’s and Parkinson’s disease [4–6]. Hence, the regulation of an inflammatory response is an active field of research. New players or novel functions of old players continue to be identified and we are only beginning to understand their specific function at the corresponding level during inflammation. Hydrogen peroxide is an example of a molecule with a long known function for pathogen clearance in inflammation. Here, we discuss how recent work using the zebrafish model has revealed a pivotal role of hydrogen peroxide in mounting an inflammatory response.
2. Cellular Lifecycle of Hydrogen Peroxide
Hydrogen peroxide belongs to a group of chemically reactive molecules known as reactive oxygen species (ROS) that arise through oxidative metabolism. ROS comprise oxygen derived small molecules such as the oxygen radicals: superoxide, hydroxyl, peroxyl, and alkoxyl; or the nonradicals: hypochlorous acid, ozone, singlet oxygen, and the current topic in focus, hydrogen peroxide [7]. ROS generation can either occur as a by-product of cellular metabolism (e.g., in mitochondria through autoxidation of respiratory chain components) or it can be created by enzymes with the primary function of ROS generation [8]. Enzymes capable of rapidly increasing local H2O2 levels include the family of NADPH oxidases [7] and other oxidases such as xanthine oxidase [9] and 5-lipoxygenase [10]. The mammalian NADPH oxidase family encompasses 7 members, which are NOX1-5 and DUOX1-2. To date, a single isoform of duox and four nox genes (nox1, 2, 4, 5) have been identified in the zebrafish genome [11]. Each member is capable of converting NADPH to NADP+ and then transporting the freed electrons across membranes. DUOX enzymes are capable of direct hydrogen peroxide production, while NOXes1-5 produce superoxide, which is rapidly converted to H2O2 by a separate superoxide dismutase or occurs spontaneously [12]. H2O2 may subsequently be utilised by peroxidase, such as thyroperoxidase, to produce thyroid hormones or myeloperoxidase and lactoperoxidase to generate more potent ROS. However, if not consumed, high concentrations of H2O2 may result in DNA damage and modifications of proteins, lipids and other molecules [13]. Thus, to avoid H2O2-mediated deleterious effects, excess H2O2 is usually rapidly catalysed or reduced by various antioxidant enzymes: such as glutathione peroxidase and catalase [14].
3. Functional Activities of H2O2
H2O2 is also involved in many regulatory cellular events including the activation of transcription factors, cell proliferation, and apoptosis [8]. H2O2 produced from the mitochondrial electron transport chain has been shown to play a role in haematopoietic cell differentiation and cell division in flies [15, 16]. NADPH oxidase generated H2O2 can affect cardiac differentiation [17], vascularisation [18], and angiogenesis [19]. In targeting cysteine and methionine residues of protein kinases and phosphatases, H2O2 is capable of modulating a number of principal signalling cascades including ERK, JNK, p38, MAPK, and PI3K/Akt [20, 21].
3.1. Inflammation-Related Functions
3.1.1. Respiratory Burst
The classical physiological role attributed to H2O2 is its capability to induce bacterial killing [12]. NOX2 is the enzyme responsible for phagocyte respiratory burst responses and is expressed in neutrophils, eosinophils, monocytes/macrophages, as well as nonphagocytic cells such as fibroblasts, cardiomyocytes, haematopoietic stem cells, and endothelial cells [7]. Under resting conditions neutrophil NOX2 resides in secondary granules, which upon activation of neutrophils fuse with phagosomal as well as plasma membranes [22].
The NADPH-oxidase-mediated respiratory burst response of neutrophils generates two superoxide anions by transporting two electrons from one NADPH across the membrane to the extracellular or intra-phagosomal space. Superoxide is further converted into hydrogen peroxide either through spontaneous dismutation, which involves the consumption of two protons, or facilitated by the catalytic activity of superoxide dismutase. Hydrogen peroxide alone and in conjunction with the amplification activity of myeloperoxidase (MPO) is responsible for bacterial killing [23, 24]. MPO, which is abundantly present in phagocyte granules, catalyses the conversion of halides and pseudohalides such as Cl−, I−, Br−, and SCN− to form hypohalous acids or pseudohypohalous acids. HOCl, however, is the primary MPO product in neutrophils responsible for bacterial killing.
3.1.2. Hydrogen Peroxide Mounting an Inflammatory Response
Recent advances accomplished by utilising the model organism zebrafish greatly expanded our view of H2O2 mediated cellular activities. The optical transparency of zebrafish larvae offers the unique advantage of real-time monitoring an immune response in a whole animal context. This is in contrast to in vitro studies and/or end-point analyses of stained tissues. Additionally, a recently developed genetically encoded H2O2 sensor provided an elegant solution for investigating the role of hydrogen peroxide dynamics during an immune response in vivo [25].
The previous view on the critical mechanisms in immediate inflammation focused on the activity of damage-associated molecular patterns (DAMPs) and pathogen-associated molecular patterns (PAMPs). Tissue damage results in the release of intracellular DAMPs usually hidden from the immune system (i.e., ATP, uric acid, lipids, DNA, nuclear proteins) or extracellular DAMPs released through degradation of extracellular matrix upon tissue injury (i.e., hyaluronan, byglycan, heparan sulfate). The receiving cell senses these signals through 5 different types of pattern recognition receptors (PRRs). Activation of these receptors in turn activates downstream NFkB, MAPK, or type I interferon-signalling pathways that are important for inflammatory and antimicrobial responses. The significance of DAMPs, PAMPs, and PRRs is comprehensively reviewed elsewhere [26, 27]. However, the mechanisms for immediate immune cell recruitment were not well defined.
Recently, Niethammer et al. described for the first time that wounded epithelium of zebrafish larvae produces a tissue-scale gradient of H2O2 mediating leukocyte recruitment [28]. This finding was in contrast to the prevalent view that leukocytes undergoing an oxidative burst response were the only source of H2O2 at a site of trauma or infection [29]. The authors employed the genetically encoded ratiometric HyPer sensor to visualise H2O2 in vivo and in real time. HyPer consists of the bacterial H2O2-sensitive transcription factor, OxyR, fused to a circularly permutated yellow fluorescent protein (YFP). Cysteine oxidation of OxyR induces a conformational change in the YFP that increases emission excited at 500 nm and decreases emission excited at 420 nm. This change is rapidly reversible within the reducing cytoplasmic environment, which allows dynamic monitoring of the intracellular hydrogen peroxide concentration [30].
Tailfin transection on zebrafish larvae induced a rapid increase in H2O2 levels extending approximately 100–200 μm from the wound margin as a decreasing concentration gradient. Furthermore, gradient formation preceded leukocyte arrival at the scene and H2O2 levels started to decrease again with accumulation of immune cells. Generation of the gradient as well as leukocyte recruitment was dependent on the activity of Duox in epithelial cells. Both, genetic knockdown of Duox and chemical inhibition of oxidase activity abolished gradient formation and significantly decreased absolute numbers of leukocytes at the wound margin, without affecting general cellular motility. These findings were corroborated by a study in drosophila focusing on prioritising competing signals by migrating macrophages [31] emphasising the crucial role of the tissue scale gradient of H2O2 for leukocyte attraction.
A study, also using zebrafish larvae, demonstrated that newly oncogene-transformed cells and their neighbours attracted leukocytes through H2O2 signalling. Utilising the H2O2-indicating dye, acetyl-pentafluorobenzene sulphonyl fluorescein, and 5,5-dimethyl-l-pyrroline N-oxide (DMPO) that reports a history of ROS exposure, it was shown that H2O2 was stochastically and momentarily produced around V12RAS expressing cells in the epidermis. Like wounded epithelial cells, transformed cells generated H2O2 in a Duox dependent manner, highlighting parallels between oncogene-transformed cells and mechanical induced injury initiation of the host inflammatory response [32].
3.1.3. Hydrogen Peroxide as a Signalling Molecule in Inflammation
Functional roles of H2O2 during inflammation have been observed previously. Mechanistically, hydrogen peroxide can modulate protein function by reversible chemical modification of protein thiols, which can result in conformational changes affecting DNA binding, enzymatic activity, multimerisation, or protein complex formation. For example, the NFkB/Rel family, key regulatory molecules in the transcription of many genes involved in inflammation, is a well-known redox-sensitive transcription factor family [33]. H2O2-induced activation of NFkB, which includes tyrosine phosphorylation of IkB and activation of IKK by H2O2 has been reported [34, 35]. Moreover, H2O2 can activate the release of high mobility group 1 protein from macrophages resulting in amplification of proinflammatory stimuli [36] or modulate leukocyte adhesion molecule expression and leukocyte endothelial adhesion [29]. VCAM-1, an endothelial scaffold on which leukocytes migrate, can activate signals in endothelial cells required for VCAM-1-dependent leukocyte migration. Leukocyte binding to VCAM-1 stimulates NOX2 in endothelial cells, resulting in the generation of H2O2, which locally activates matrix metalloproteinases (MMPs). These MMPs in turn degrade matrix and endothelial cell surface receptors in cell junctions facilitating leukocyte transendothelial migration [37, 38].
These examples show how H2O2 can act as an intracellular or local signalling molecule but long-distance intercellular mechanisms of H2O2-mediated leukocyte recruitment were less well defined.
The open question of how leukocytes may receive the signal to initiate directional migration was recently addressed in another elegant study using the zebrafish model by Yoo et al. [39]. They have identified the SRC family kinase (SFK) Lyn as a redox sensor in neutrophils that detects hydrogen peroxide emanating from wounds and guiding their migration. Yoo and colleagues were able to provide direct evidence for punctate SFK activation at the leading edge of neutrophils in response to wounding. Through the knockdown of Duox, which is responsible for H2O2 production at the wound margin, they have explored the role of H2O2 in SFK activation. Duox knockdown prevented SFK phosphorylation indicating that activation of neutrophil SFKs may be dependent on the presence of hydrogen peroxide levels at wounds. Further evidence suggesting that SFKs can act as a redox sensor was provided by utilisation of SFK inhibitors that resulted in impairment of early neutrophil accumulation, while having no effect on epithelial hydrogen peroxide bursts [39].
Profiling SFK family members in zebrafish myeloid cells identified the Lyn kinase as a promising candidate acting as the redox sensor in neutrophils and macrophages. Morpholino knockdown of Lyn impaired directional migration of neutrophils to a tailfin wound in zebrafish larvae.
Further in vitro investigation revealed that hydrogen peroxide directly activates Lyn through the oxidation of Cys466, leading to downstream signalling, for example, Erk activation. This in vitro evidence was elegantly confirmed in vivo using a combination of genetic knockdown of Lyn and neutrophil-specific transgenic reconstitution of a Cys466 mutant or wild-type Lyn-GFP fusion.
In conclusion, these two sophisticated studies demonstrated a novel role of H2O2 as mediator of immediate inflammation and revealed aspects of the mechanisms resulting in leukocyte recruitment to a site of trauma (Figure 1). Evidence is accumulating that H2O2 signalling to phagocytes is a widely conserved mechanism present not only in zebrafish [28, 32, 39] but also flies [31] and mammals [39, 40].
4. Outlook
The discovery of a new biological mechanism opens up a new line of research and poses numerous new questions to address. The most obvious being: How is Duox activated in epithelial cells upon wounding and how is the H2O2 gradient resolved? One hypothesis would place calcium as the immediate injury signal to the wounded cell in order to produce hydrogen peroxide through Duox. Physical disruption of plasma membranes results in an uncontrolled influx of calcium [41]. Giving credence to this hypothesis, evidence exists showing that DUOX activation by calcium regulates H2O2 generation [42].
In order to avoid excess tissue damage and persistent granulocyte recruitment/retention, the presence of the hydrogen peroxide gradient must be tightly regulated. Regulation could occur on the enzymatic level in terms of H2O2 production as well as on the molecular level in terms of H2O2 stability. Oxidase activity results in membrane depolarisation due to the electrogenic properties of the enzymes to the point of NADPH oxidase inhibition. Prolonged H2O2 production depletes the NADPH pools, which may automatically result in cessation of H2O2 generation. Alternatively or in addition, neutrophil MPO could be responsible for the decrease in hydrogen peroxide levels upon arrival at the wound [24].
This mechanism suggests new approaches to therapeutically modulate both the onset of the cellular inflammatory response and its resolution, particularly as it involves a small, relatively unstable signalling molecule and is dependent on multiple enzymatic steps amenable to pharmacologic intervention.
Authors’ Contribution
C. Wittman and P. Chockley contributed equally to this paper.
Acknowledgments
CW was supported by a PhD fellowship from the Helmholtz program “BioInterfaces international graduate school” (BIFIGS). Further support was provided by a KIT-RISC grant and by a Marie Curie International Reintegration Grant within the 7th European Community Framework Program (PIRG07-GA-2010-267552) to CG. The Australian Regenerative Medicine Institute is supported by grants from the State Government of Victoria and the Australian Government.