β-Catenin Signaling Biases Multipotent Lingual Epithelial Progenitors to Differentiate and Acquire Specific Taste Cell Fates
Taste is a fundamental sense that helps the body determine whether food can be ingested. Taste dysfunction can be a side effect of cancer therapies, can result from an alteration of the renewal capacities of the taste buds, and is often associated with psychological distress and malnutrition. Thus, understanding how taste cells renew throughout adult life, i.e. how newly born cells replace old cells as they die, is essential to find potential therapeutic targets to improve taste sensitivity in patients suffering taste dysfunction. Here we show that a specific molecular pathway, Wnt/β-catenin signaling, controls renewal of taste cells by regulating separate stages of taste cell turnover. We show that activating this pathway directs the newly born cells to become primarily a specific taste cell type whose role is to support the other taste cells and help them work efficiently.
Vyšlo v časopise:
β-Catenin Signaling Biases Multipotent Lingual Epithelial Progenitors to Differentiate and Acquire Specific Taste Cell Fates. PLoS Genet 11(5): e32767. doi:10.1371/journal.pgen.1005208
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pgen.1005208
Souhrn
Taste is a fundamental sense that helps the body determine whether food can be ingested. Taste dysfunction can be a side effect of cancer therapies, can result from an alteration of the renewal capacities of the taste buds, and is often associated with psychological distress and malnutrition. Thus, understanding how taste cells renew throughout adult life, i.e. how newly born cells replace old cells as they die, is essential to find potential therapeutic targets to improve taste sensitivity in patients suffering taste dysfunction. Here we show that a specific molecular pathway, Wnt/β-catenin signaling, controls renewal of taste cells by regulating separate stages of taste cell turnover. We show that activating this pathway directs the newly born cells to become primarily a specific taste cell type whose role is to support the other taste cells and help them work efficiently.
Zdroje
1. Roper SD. The cell biology of vertebrate taste receptors. Annual review of neuroscience. 1989;12:329–53. 2648951
2. Barlow LA, Northcutt RG. Embryonic Origin of Amphibian Taste Buds. Developmental Biology. 1995;169(1):273–85. 7750643
3. Stone LM, Finger TE, Tam PP, Tan SS. Taste receptor cells arise from local epithelium, not neurogenic ectoderm. Proceedings of the National Academy of Sciences. 1995;92(6):1916–20. 7892199
4. Liu H- X, Komatsu Y, Mishina Y, Mistretta CM. Neural crest contribution to lingual mesenchyme, epithelium and developing taste papillae and taste buds. Developmental Biology. 2012;368(2):294–303. doi: 10.1016/j.ydbio.2012.05.028 22659543
5. Feng P, Huang L, Wang H. Taste Bud Homeostasis in Health, Disease, and Aging. Chemical senses. 2014;39(1):3–16. doi: 10.1093/chemse/bjt059 24287552
6. Okubo T, Clark C, Hogan BL. Cell lineage mapping of taste bud cells and keratinocytes in the mouse tongue and soft palate. Stem cells (Dayton, Ohio). 2009;27(2):442–50. doi: 10.1634/stemcells.2008-0611 19038788
7. Presland RB, Dale BA. Epithelial Structural Proteins of the Skin and Oral Cavity: Function in Health and Disease. Critical Reviews in Oral Biology & Medicine. 2000;11(4):383–408. doi: 10.1186/s12967-014-0362-3 25592846
8. Hill MW. Influence of age on the morphology and transit time of murine stratified squamous epithelia. Archives of oral biology. 1988;33(4):221–9. 3165257
9. Potten CS, Booth D, Cragg NJ, O'Shea JA, Tudor GL, Booth C. Cell kinetic studies in murine ventral tongue epithelium: cell cycle progression studies using double labelling techniques. Cell proliferation. 2002;35:16–21. 12139704
10. Moore KA, Lemischka IR. Stem Cells and Their Niches. Science. 2006;311(5769):1880–5. 16574858
11. Creamer B, Shorter RG, Bamforth J. The turnover and shedding of epithelial cells. I. The turnover in the gastro-intestinal tract. Gut. 1961;2:110–8. 13696345
12. Potten CS, Saffhill R, Maibach HI. Measurement of the transit time for cells through the epidermis and stratum corneum of the mouse and guinea-pig. Cell proliferation. 1987;20(5):461–72. 3450396
13. Beidler LM, Smallman RL. Renewal of cells within taste buds. The Journal of cell biology. 1965;27(2):263–72. 5884625
14. Farbman AI. Renewal of taste bud cells in rat circumvallate papillae. Cell and tissue kinetics. 1980;13(4):349–57. 7428010
15. Hamamichi R, Asano-Miyoshi M, Emori Y. Taste bud contains both short-lived and long-lived cell populations. Neuroscience. 2006;141(4):2129–38. 16843606
16. Perea-Martinez I, Nagai T, Chaudhari N. Functional Cell Types in Taste Buds Have Distinct Longevities. PLoS ONE. 2013;8(1):e53399. doi: 10.1371/journal.pone.0053399 23320081
17. Vandenbeuch A, Clapp TR, Kinnamon SC. Amiloride-sensitive channels in type I fungiform taste cells in mouse. BMC Neurosci. 2008;9:1. doi: 10.1186/1471-2202-9-1 18171468
18. Chaudhari N, Roper SD. The cell biology of taste. The Journal of cell biology. 2010;190(3):285–96. doi: 10.1083/jcb.201003144 20696704
19. Ma H, Yang R, Thomas S, Kinnamon J. Qualitative and quantitative differences between taste buds of the rat and mouse. BMC Neuroscience. 2007;8(1):5.
20. Ohtubo Y, Yoshii K. Quantitative analysis of taste bud cell numbers in fungiform and soft palate taste buds of mice. Brain Research. 2011;1367:13–21. doi: 10.1016/j.brainres.2010.10.060 20971092
21. Miura H, Kusakabe Y, Harada S. Cell lineage and differentiation in taste buds. Archives of histology and cytology. 2006;69(4):209–25. 17287576
22. Miura H, Scott JK, Harada S, Barlow LA. Sonic hedgehog-expressing basal cells are general post-mitotic precursors of functional taste receptor cells. Developmental Dynamics. 2014;243(10):1286–97. doi: 10.1002/dvdy.24121 24590958
23. Liu F, Thirumangalathu S, Gallant NM, Yang SH, Stoick-Cooper CL, Reddy ST, et al. Wnt-beta-catenin signaling initiates taste papilla development. Nature genetics. 2007;39(1):106–12. 17128274
24. Iwatsuki K, Liu H- X, Gründer A, Singer MA, Lane TF, Grosschedl R, et al. Wnt signaling interacts with Shh to regulate taste papilla development. Proceedings of the National Academy of Sciences. 2007;104(7):2253–8. 17284610
25. Choi Yeon S, Zhang Y, Xu M, Yang Y, Ito M, Peng T, et al. Distinct Functions for Wnt/β-Catenin in Hair Follicle Stem Cell Proliferation and Survival and Interfollicular Epidermal Homeostasis. Cell stem cell. 2013;13(6):720–33. doi: 10.1016/j.stem.2013.10.003 24315444
26. Widelitz RB, Jiang T-X, Lu J, Chuong C-M. β-catenin in Epithelial Morphogenesis: Conversion of Part of Avian Foot Scales into Feather Buds with a Mutated β-Catenin. Developmental Biology. 2000;219(1):98–114. 10677258
27. Harada N, Tamai Y, Ishikawa T-o, Sauer B, Takaku K, Oshima M, et al. Intestinal polyposis in mice with a dominant stable mutation of the [beta]-catenin gene. EMBO J. 1999;18(21):5931–42. 10545105
28. Sangiorgi E, Capecchi MR. Bmi1 is expressed in vivo in intestinal stem cells. Nature genetics. 2008;40(7):915–20. doi: 10.1038/ng.165 18536716
29. Sansom OJ, Reed KR, Hayes AJ, Ireland H, Brinkmann H, Newton IP, et al. Loss of Apc in vivo immediately perturbs Wnt signaling, differentiation, and migration. Genes & Development. 2004;18(12):1385–90.
30. Varela-Nallar L, Inestrosa NC. Wnt signaling in the regulation of adult hippocampal neurogenesis. Frontiers in cellular neuroscience. 2013;7(100):1–11.
31. Gaillard D, Barlow LA. Taste bud cells of adult mice are responsive to Wnt/β-catenin signaling: Implications for the renewal of mature taste cells. Genesis. 2011;49(4):295–306. doi: 10.1002/dvg.20731 21328519
32. Rothova M, Thompson H, Lickert H, Tucker AS. Lineage tracing of the endoderm during oral development. Developmental Dynamics. 2012;241(7):1183–91. doi: 10.1002/dvdy.23804 22581563
33. Asano-Miyoshi M, Hamamichi R, Emori Y. Cytokeratin 14 is expressed in immature cells in rat taste buds. Journal of molecular histology. 2008;39(2):193–9. 17960487
34. Iwasaki S, Aoyagi H, Yoshizawa H. Localization of keratins 13 and 14 in the lingual mucosa of rats during the morphogenesis of circumvallate papillae. Acta histochemica. 2011;113(4):395–401. doi: 10.1016/j.acthis.2010.03.003 20546859
35. Zhang C, Cotter M, Lawton A, Oakley B, Wong L, Zeng Q. Keratin 18 is associated with a subset of older taste cells in the rat. Differentiation; research in biological diversity. 1995;59(3):155–62. 7589899
36. Miura H, Kusakabe Y, Sugiyama C, Kawamatsu M, Ninomiya Y, Motoyama J, et al. Shh and Ptc are associated with taste bud maintenance in the adult mouse. Mech Dev. 2001;106(1–2):143–5. 11472849
37. Liu HX, Ermilov A, Grachtchouk M, Li L, Gumucio DL, Dlugosz AA, et al. Multiple Shh signaling centers participate in fungiform papilla and taste bud formation and maintenance. Developmental Biology. 2013;382(1):82–97. doi: 10.1016/j.ydbio.2013.07.022 23916850
38. Shin K, Fogg VC, Margolis B. Tight Junctions and Cell Polarity. Annual Review of Cell and Developmental Biology. 2006;22(1):207–35.
39. Van Itallie C, Rahner C, Anderson JM. Regulated expression of claudin-4 decreases paracellular conductance through a selective decrease in sodium permeability. J Clin Invest. 2001;107(10):1319–27. 11375422
40. Michlig S, Damak S, Le Coutre J. Claudin-based permeability barriers in taste buds. The Journal of comparative neurology. 2007;502(6):1003–11. 17447253
41. Castillo D, Seidel K, Salcedo E, Ahn C, de Sauvage FJ, Klein OD, et al. Induction of ectopic taste buds by SHH reveals the competency and plasticity of adult lingual epithelium. Development. 2014;141(15):2993–3002. doi: 10.1242/dev.107631 24993944
42. Hosley MA, Oakley B. Postnatal development of the vallate papilla and taste buds in rats. The Anatomical record. 1987;218(2):216–22. 3619089
43. Bradley RM, Stern IB. The development of the human taste bud during the foetal period. Journal of anatomy. 1967;101(Pt 4):743–52.
44. Belecky TL, Smith DV. Postnatal development of palatal and laryngeal taste buds in the hamster. The Journal of comparative neurology. 1990;293(4):646–54. 2329198
45. Mbiene JP, Farbman AI. Evidence for stimulus access to taste cells and nerves during development: an electron microscopic study. Microscopy research and technique. 1993;26(2):94–105. 8241557
46. Nguyen HM, Reyland ME, Barlow LA. Mechanisms of taste bud cell loss after head and neck irradiation. J Neurosci. 2012;32(10):3474–84. doi: 10.1523/JNEUROSCI.4167-11.2012 22399770
47. Yang R, Crowley HH, Rock ME, Kinnamon JC. Taste cells with synapses in rat circumvallate papillae display SNAP-25-like immunoreactivity. The Journal of comparative neurology. 2000;424(2):205–15. 10906698
48. Clapp TR, Yang R, Stoick CL, Kinnamon SC, Kinnamon JC. Morphologic characterization of rat taste receptor cells that express components of the phospholipase C signaling pathway. The Journal of comparative neurology. 2004;468(3):311–21. 14681927
49. Bartel DL, Sullivan SL, Lavoie EG, Sevigny J, Finger TE. Nucleoside triphosphate diphosphohydrolase-2 is the ecto-ATPase of type I cells in taste buds. The Journal of comparative neurology. 2006;497(1):1–12. 16680780
50. Lawton DM, Furness DN, Lindemann B, Hackney CM. Localization of the glutamate-aspartate transporter, GLAST, in rat taste buds. The European journal of neuroscience. 2000;12(9):3163–71. 10998100
51. Pumplin DW, Yu C, Smith DV. Light and dark cells of rat vallate taste buds are morphologically distinct cell types. The Journal of comparative neurology. 1997;378(3):389–410. 9034899
52. Seta Y, Oda M, Kataoka S, Toyono T, Toyoshima K. Mash1 is required for the differentiation of AADC-positive type III cells in mouse taste buds. Dev Dyn. 2011;240(4):775–84. doi: 10.1002/dvdy.22576 21322090
53. Kito-Shingaki A, Seta Y, Toyono T, Kataoka S, Kakinoki Y, Yanagawa Y, et al. Expression of GAD67 and Dlx5 in the Taste Buds of Mice Genetically Lacking Mash1. Chemical senses. 2014;39(5):403–14. doi: 10.1093/chemse/bju010 24682237
54. Matsumoto I, Ohmoto M, Narukawa M, Yoshihara Y, Abe K. Skn-1a (Pou2f3) specifies taste receptor cell lineage. Nature neuroscience. 2011;14(6):685–7. doi: 10.1038/nn.2820 21572433
55. Gat U, DasGupta R, Degenstein L, Fuchs E. De Novo hair follicle morphogenesis and hair tumors in mice expressing a truncated beta-catenin in skin. Cell. 1998;95(5):605–14. 9845363
56. Lim X, Tan SH, Koh WLC, Chau RMW, Yan KS, Kuo CJ, et al. Interfollicular Epidermal Stem Cells Self-Renew via Autocrine Wnt Signaling. Science. 2013;342(6163):1226–30. doi: 10.1126/science.1239730 24311688
57. Lien W-H, Fuchs E. Wnt some lose some: transcriptional governance of stem cells by Wnt/β-catenin signaling. Genes & Development. 2014;28(14):1517–32.
58. Clevers H. The Intestinal Crypt, A Prototype Stem Cell Compartment. Cell. 2013;154(2):274–84. doi: 10.1016/j.cell.2013.07.004 23870119
59. Andreu P, Peignon G, Slomianny C, Taketo MM, Colnot S, Robine S, et al. A genetic study of the role of the Wnt/β-catenin signalling in Paneth cell differentiation. Developmental Biology. 2008;324(2):288–96. doi: 10.1016/j.ydbio.2008.09.027 18948094
60. Lowry WE, Blanpain C, Nowak JA, Guasch G, Lewis L, Fuchs E. Defining the impact of beta-catenin/Tcf transactivation on epithelial stem cells. Genes Dev. 2005;19(13):1596–611. 15961525
61. Zhang Y, Andl T, Yang SH, Teta M, Liu F, Seykora JT, et al. Activation of beta-catenin signaling programs embryonic epidermis to hair follicle fate. Development. 2008;135(12):2161–72. doi: 10.1242/dev.017459 18480165
62. Lien W- H, Polak L, Lin M, Lay K, Zheng D, Fuchs E. In vivo transcriptional governance of hair follicle stem cells by canonical Wnt regulators. Nature cell biology. 2014;16(2):179–90. doi: 10.1038/ncb2903 24463605
63. Clevers H. Wnt/[beta]-Catenin Signaling in Development and Disease. Cell. 2006;127(3):469–80. 17081971
64. Northcutt RG. Taste Buds: Development and Evolution. Brain, Behavior and Evolution. 2004;64(3):198–206. 15353910
65. Nguyen HM, Barlow LA. BMP4 expression differs in anterior fungiform versus posterior circumvallate taste buds of mice. BMC Neurosci. 2010;11(1):129.
66. Petersen CI, Jheon AH, Mostowfi P, Charles C, Ching S, Thirumangalathu S, et al. FGF Signaling Regulates the Number of Posterior Taste Papillae by Controlling Progenitor Field Size. PLoS genetics. 2011;7(6):e1002098. doi: 10.1371/journal.pgen.1002098 21655085
67. Kist R, Watson M, Crosier M, Robinson M, Fuchs J, Reichelt J, et al. The formation of endoderm-derived taste sensory organs requires a pax9-dependent expansion of embryonic taste bud progenitor cells. PLoS genetics. 2014;10(10):e1004709. doi: 10.1371/journal.pgen.1004709 25299669
68. Chai R, Xia A, Wang T, Jan TA, Hayashi T, Bermingham-McDonogh O, et al. Dynamic Expression of Lgr5, a Wnt Target Gene, in the Developing and Mature Mouse Cochlea. JARO. 2011;12(4):455–69. doi: 10.1007/s10162-011-0267-2 21472479
69. Yamamoto S, Nakase H, Matsuura M, Honzawa Y, Matsumura K, Uza N, et al. Heparan sulfate on intestinal epithelial cells plays a critical role in intestinal crypt homeostasis via Wnt/beta-catenin signaling. Am J Physiol Gastrointest Liver Physiol. 2013;305(3):G241–9. doi: 10.1152/ajpgi.00480.2012 23744737
70. Takeda N, Jain R, Li D, Li L, Lu MM, Epstein JA. Lgr5 Identifies Progenitor Cells Capable of Taste Bud Regeneration after Injury. PLoS ONE. 2013;8(6):e66314. 23824276
71. Yee KK, Li Y, Redding KM, Iwatsuki K, Margolskee RF, Jiang P. Lgr5-EGFP Marks Taste Bud Stem/Progenitor Cells in Posterior Tongue. Stem cells (Dayton, Ohio). 2013:N/A-N/A.
72. Zhang GH, Zhang HY, Deng SP, Qin YM. Regional differences in taste bud distribution and alpha-gustducin expression patterns in the mouse fungiform papilla. Chemical senses. 2008;33(4):357–62. doi: 10.1093/chemse/bjm093 18296428
73. Sandow PL, Hejrat-Yazdi M, Heft MW. Taste Loss and Recovery Following Radiation Therapy. Journal of dental research. 2006;85(7):608–11. 16798859
74. Ruat M, Hoch L, Faure H, Rognan D. Targeting of Smoothened for therapeutic gain. Trends in Pharmacological Sciences. 2014;35(5):237–46. doi: 10.1016/j.tips.2014.03.002 24703627
75. Diamond I, Owolabi T, Marco M, Lam C, Glick A. Conditional Gene Expression in the Epidermis of Transgenic Mice Using the Tetracycline-Regulated Transactivators tTA and rTA Linked to the Keratin 5 Promoter. J Invest Dermatol. 2000;115(5):788–94. 11069615
76. Perl A- KT, Wert SE, Nagy A, Lobe CG, Whitsett JA. Early restriction of peripheral and proximal cell lineages during formation of the lung. Proceedings of the National Academy of Sciences of the United States of America. 2002;99(16):10482–7. 12145322
77. Soriano P. Generalized lacZ expression with the ROSA26 Cre reporter strain. Nature genetics. 1999;21(1):70–1. 9916792
78. Harfe BD, Scherz PJ, Nissim S, Tian H, McMahon AP, Tabin CJ. Evidence for an Expansion-Based Temporal Shh Gradient in Specifying Vertebrate Digit Identities. Cell. 2004;118(4):517–28. 15315763
79. Srinivas S, Watanabe T, Lin C-S, William C, Tanabe Y, Jessell T, et al. Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus. BMC Developmental Biology. 2001;1(1):4.
80. Kim EJ, Battiste J, Nakagawa Y, Johnson JE. Ascl1 (Mash1) lineage cells contribute to discrete cell populations in CNS architecture. Molecular and Cellular Neuroscience. 2008;38(4):595–606. doi: 10.1016/j.mcn.2008.05.008 18585058
81. Kitamura K, Miura H, Yanazawa M, Miyashita T, Kato K. Expression patterns of Brx1 (Rieg gene), Sonic hedgehog, Nkx2.2, Dlx1 and Arx during zona limitans intrathalamica and embryonic ventral lateral geniculate nuclear formation. Mech Dev. 1997;67(1):83–96. 9347917
82. Kokovay E, Wang Y, Kusek G, Wurster R, Lederman P, Lowry N, et al. VCAM1 Is Essential to Maintain the Structure of the SVZ Niche and Acts as an Environmental Sensor to Regulate SVZ Lineage Progression. Cell stem cell. 2012;11(2):220–30. doi: 10.1016/j.stem.2012.06.016 22862947
83. Ceradini DJ, Kulkarni AR, Callaghan MJ, Tepper OM, Bastidas N, Kleinman ME, et al. Progenitor cell trafficking is regulated by hypoxic gradients through HIF-1 induction of SDF-1. Nat Med. 2004;10(8):858–64. 15235597
84. Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods (San Diego, Calif. 2001;25(4):402–8. 11846609
85. Braet F, De Zanger R, Wisse E. Drying cells for SEM, AFM and TEM by hexamethyldisilazane: a study on hepatic endothelial cells. Journal of microscopy. 1997;186(Pt 1):84–7.
86. Yoshie S, Wakasugi C, Teraki Y, Fujita T. Fine structure of the taste bud in guinea pigs. I. Cell characterization and innervation patterns. Archives of histology and cytology. 1990;53(1):103–19. 2364007
87. Gavet O, Pines J. Progressive Activation of CyclinB1-Cdk1 Coordinates Entry to Mitosis. Developmental Cell. 2010;18(4):533–43. doi: 10.1016/j.devcel.2010.02.013 20412769
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Genetika Reprodukčná medicínaČlánok vyšiel v časopise
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