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Dermatology Research and Practice
Volume 2013 (2013), Article ID 359756, 14 pages
Tamarind Seed Xyloglucans Promote Proliferation and Migration of Human Skin Cells through Internalization via Stimulation of Proproliferative Signal Transduction Pathways
Westfalian Wilhelms University of Muenster, Institute for Pharmaceutical Biology and Phytochemistry, Hittorfstraße 56, 48149 Muenster, Germany
Received 14 March 2013; Revised 9 June 2013; Accepted 23 June 2013
Academic Editor: Lajos Kemeny
Copyright © 2013 W. Nie and A. M. Deters. 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.
- S. C. Fry, “The structure and functions of xyloglucan,” Journal of Experimental Botany, vol. 40, no. 1, pp. 1–11, 1989.
- C. Niemann, N. C. Carpita, and R. L. Whistler, “Arabinose-containing oligosaccharides from tamarind xyloglucan,” Starch/Staerke, vol. 49, no. 4, pp. 154–159, 1997.
- E. Abraham Tholath and K. S. Ghandroth, “Transparent Xyloglucan/Chitosan Gel and a Process for the Preparation Thereof,” US 20120009132 A1, 2012.
- A. M. Avachat, K. N. Gujar, and K. V. Wagh, “Development and evaluation of tamarind seed xyloglucan-based mucoadhesive buccal films of rizatriptan benzoate,” Carbohydrate Polymers, vol. 91, pp. 537–542, 2013.
- D. Pal and A. K. Nayak, “Novel tamarind seed polysaccharide-alginate mucoadhesive microspheres for oral gliclazide delivery: in vitro-in vivo evaluation,” Drug Delivery, vol. 19, no. 3, pp. 123–131, 2012.
- D. Chen, P. Guo, S. Chen et al., “Properties of xyloglucan hydrogel as the biomedical sustained-release carriers,” Journal of Materials Science, vol. 23, pp. 955–962, 2012.
- G. Uccello-Barretta, S. Nazzi, Y. Zambito, G. Di Colo, F. Balzano, and M. Sansò, “Synergistic interaction between TS-polysaccharide and hyaluronic acid: implications in the formulation of eye drops,” International Journal of Pharmaceutics, vol. 395, no. 1-2, pp. 122–131, 2010.
- A. Takahashi, S. Suzuki, N. Kawasaki et al., “Percutaneous absorption of non-steroidal anti-inflammatory drugs from in situ gelling xyloglucan formulations in rats,” International Journal of Pharmaceutics, vol. 246, no. 1-2, pp. 179–186, 2002.
- H. S. Mahajan, V. Tyagi, G. Lohiya, and P. Nerkar, “Thermally reversible xyloglucan gels as vehicles for nasal drug delivery,” Drug Delivery, vol. 19, no. 5, pp. 270–276, 2012.
- F. M. Strickland, Y. Sun, A. Darvill, S. Eberhard, M. Pauly, and P. Albersheim, “Preservation of the delayed-type hypersensitivity response to alloantigen by xyloglucans or oligogalacturonide does not correlate with the capacity to reject ultraviolet-induced skin tumors in mice,” The Journal of Investigative Dermatology, vol. 116, no. 1, pp. 62–68, 2001.
- S. R. Aravind, M. M. Joseph, S. Varghese, P. Balaram, and T. T. Sreelekha, “Antitumor and immunopotentiating activity of polysaccharide PST001 isolated from the seed kernel of Tamarindus indica: an in vivo study in mice,” The Scientific World Journal, vol. 2012, Article ID 361382, 14 pages, 2012.
- M. M. T. do Rosário, M. M. Kangussu-Marcolino, A. E. do Amaral, G. R. Noleto, and C. L. D. O. Petkowicz, “Storage xyloglucans: potent macrophages activators,” Chemico-Biological Interactions, vol. 189, no. 1-2, pp. 127–133, 2011.
- T. Komutarin, S. Azadi, L. Butterworth et al., “Extract of the seed coat of Tamarindus indica inhibits nitric oxide production by murine macrophages in vitro and in vivo,” Food and Chemical Toxicology, vol. 42, no. 4, pp. 649–658, 2004.
- S. Burgalassi, L. Raimondi, R. Pirisino, G. Banchelli, E. Boldrini, and M. F. Saettone, “Effect of xyloglucan (tamarind seed polysaccharide) on conjunctival cell adhesion to laminin and on corneal epithelium wound healing,” European Journal of Ophthalmology, vol. 10, no. 1, pp. 71–76, 2000.
- M. Rolando and C. Valente, “Establishing the tolerability and performance of tamarind seed polysaccharide (TSP) in treating dry eye syndrome: results of a clinical study,” BMC Ophthalmology, vol. 7, article 5, 2007.
- M. Y. Bin Mohamad, H. B. Akram, D. N. Bero, and M. T. Rahman, “Tamarind seed extract enhances epidermal wound healing,” International Journal of Biology, vol. 4, pp. 81–88, 2012.
- J. M. Kuchel, R. S. C. Barnetson, L. Zhuang, P. M. Strickland, R. P. Pelley, and G. M. Halliday, “Tamarind inhibits solar-simulated ultraviolet radiation-induced suppression of recall responses in humans,” Letters in Drug Design & Discovery, vol. 2, no. 2, pp. 165–171, 2005.
- T. K. Hunt, “The physiology of wound healing,” Annals of Emergency Medicine, vol. 17, no. 12, pp. 1265–1273, 1988.
- W. Mutschler, “Physiology and pathophysiology of wound healing of wound defects,” Der Unfallchirurg, vol. 115, pp. 767–773, 2012.
- M. Maas, M. Kemper, F. Lamerding, A. Klenke, and A. Deters, “Variations in extraction protocol lead to differences in monosaccharide composition and bioactivity on human keratinocytes as shown by polysaccharides from banana and plum fruits,” Planta Medica, vol. 72, p. 237, 2006.
- C. Junchen, L. Pufu, S. Hengsheng, Z. Hengguang, and F. Rutao, “Effect of extraction methods on polysaccharide of clitocybe maxima stipe,” Advance Journal of Food Science and Technology, vol. 5, pp. 370–373, 2013.
- H. C. Srivastava and P. P. Singh, “Structure of the polysaccharide from tamarind kernel,” Carbohydrate Research, vol. 4, no. 4, pp. 326–342, 1967.
- A. M. Deters, K. R. Schröder, T. Smiatek, and A. Hensel, “Ispaghula (Plantago ovata) seed husk polysaccharides promote proliferation of human epithelial cells (skin keratinocytes and fibroblasts) via enhanced growth factor receptors and energy production,” Planta Medica, vol. 71, no. 1, pp. 33–39, 2005.
- M. Monsigny, C. Petit, and A.-C. Roche, “Colorimetric determination of neutral sugars by a resorcinol sulfuric acid micromethod,” Analytical Biochemistry, vol. 175, no. 2, pp. 525–530, 1988.
- M. M. Bradford, “A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein dye binding,” Analytical Biochemistry, vol. 72, no. 1-2, pp. 248–254, 1976.
- S. Abakuks and A. M. Deters, “Polysaccharides of St. John's Wort herb stimulate NHDF proliferation and NEHK differentiation via influence on extracellular structures and signal pathways,” Advances in Pharmacology Science, vol. 2012, Article ID 304317, 11 pages, 2012.
- A. N. de Belder and K. Granath, “Preparation and properties of fluorescein-labelled dextrans,” Carbohydrate Research, vol. 30, no. 2, pp. 375–378, 1973.
- K. Gescher and A. M. Deters, “Typha latifolia L. fruit polysaccharides induce the differentiation and stimulate the proliferation of human keratinocytes in vitro,” Journal of Ethnopharmacology, vol. 137, no. 1, pp. 352–358, 2011.
- T. Mosmann, “Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays,” Journal of Immunological Methods, vol. 65, no. 1-2, pp. 55–63, 1983.
- T. Schreier, E. Degen, and W. Baschong, “Fibroblast migration and proliferation during in vitro wound healing. A quantitative comparison between various growth factors and a low molecular weight blood dialyzate used in the clinic to normalize impaired wound healing,” Research in Experimental Medicine, vol. 193, no. 4, pp. 195–205, 1993.
- M. Maas, A. M. Deters, and A. Hensel, “Anti-inflammatory activity of Eupatorium perfoliatum L. extracts, eupafolin, and dimeric guaianolide via iNOS inhibitory activity and modulation of inflammation-related cytokines and chemokines,” Journal of Ethnopharmacology, vol. 137, no. 1, pp. 371–381, 2011.
- The GeneCards Human, Crown Human Genome Center, Department of Molecular Genetics, Weizmann Institute of Science, “hostname: 356977-web1.xennexinc.com db genecards_309_100 index build: 100 solr: 1.4”.
- I. V. Yang, E. Chen, J. P. Hasseman et al., “Within the fold: assessing differential expression measures and reproducibility in microarray assays,” Genome Biology, vol. 3, no. 11, Article ID research0062, 2002.
- M. V. Berridge, P. M. Herst, and A. S. Tan, “Tetrazolium dyes as tools in cell biology: new insights into their cellular reduction,” Biotechnology Annual Review, vol. 11, pp. 127–152, 2005.
- P. Lang and K. Kajiwara, “Investigations of the architecture of tamarind seed polysaccharide in aqueous solution by different scattering techniques,” Journal of Biomaterials Science. Polymer Edition, vol. 4, no. 5, pp. 517–528, 1993.
- M. J. Gidley, P. J. Lillford, D. W. Rowlands et al., “Structure and solution properties of tamarind-seed polysaccharide,” Carbohydrate Research, vol. 214, no. 2, pp. 299–314, 1991.
- Y. Li, M. N. Corradetti, K. Inoki, and K.-L. Guan, “TSC2: filling the GAP in the mTOR signaling pathway,” Trends in Biochemical Sciences, vol. 29, no. 1, pp. 32–38, 2004.
- J. Zhou, J. Wulfkuhle, H. Zhang, et al., “Activation of the PTEN/mTOR/STAT3 pathway in breast cancer stem-like cells is required for viability and maintenance,” Proceedings of the National Academy of Sciences of the United States of America, vol. 104, pp. 16158–16163, 2007.
- R. R. Ricardo-Gonzalez, A. R. Eagle, J. I. Odegaard et al., “IL-4/STAT6 immune axis regulates peripheral nutrient metabolism and insulin sensitivity,” Proceedings of the National Academy of Sciences of the United States of America, vol. 107, no. 52, pp. 22617–22622, 2010.
- P. P. Roux and J. Blenis, “ERK and p38 MAPK-activated protein kinases: a family of protein kinases with diverse biological functions,” Microbiology and Molecular Biology Reviews, vol. 68, no. 2, pp. 320–344, 2004.
- K. A. Gallo and G. L. Johnson, “Mixed-lineage kinase control of JNK and p38 MAPK pathways,” Nature Reviews Molecular Cell Biology, vol. 3, no. 9, pp. 663–672, 2002.
- E. R. Andersson, “The role of endocytosis in activating and regulating signal transduction,” Cellular and Molecular Life Sciences, vol. 69, pp. 1755–1771, 2012.
- S. Ilangumaran, B. Borisch, and D. C. Hoessli, “Signal transduction via CD44: role of plasma membrane microdomains,” Leukemia & Lymphoma, vol. 35, no. 5-6, pp. 455–469, 1999.
- M. Krauss and V. Haucke, “Shaping membranes for endocytosis,” Reviews of Physiology, Biochemistry and Pharmacology, vol. 161, pp. 45–66, 2011.
- M. Bienz, “β-catenin: a pivot between cell adhesion and Wnt signalling,” Current Biology, vol. 15, no. 2, pp. R64–R67, 2005.
- C. R. Weston and R. J. Davis, “The JNK signal transduction pathway,” Current Opinion in Genetics and Development, vol. 12, no. 1, pp. 14–21, 2002.
- M. Sano, E. Miyata, S. Tamano, A. Hagiwara, N. Ito, and T. Shirai, “Lack of carcinogenicity of tamarind seed polysaccharide in B6C3F1 mice,” Food and Chemical Toxicology, vol. 34, no. 5, pp. 463–467, 1996.