Compensatory cellular hypertrophy: The other strategy for tissue homeostasis

Trends in Cell Biology

Volumn 24, Issue 4, 2014, Pages 230-237

  Tamori, Yoichiro ^a   Deng, Wu Min ^a  

^a FLORIDA STATE UNIVERSITY   (United States)

Author keywords

Cell competition; Compensatory cellular hypertrophy; Compensatory proliferation; Drosophila follicle cells; Postmitotic tissue; Tissue homeostasis

Indexed keywords

CASPASE 2; CYCLIN E; EFFECTOR CASPASE; INTERLEUKIN 1BETA; INTERLEUKIN 6; STRESS ACTIVATED PROTEIN KINASE;

COLUMNAR EPITHELIUM; COMPENSATORY CELLULAR HYPERTROPHY; CORNEA ENDOTHELIUM; DROSOPHILA; ENDOREDUPLICATION; EPIDERMIS; HOMEOSTASIS; HYPERTROPHY; LIVER; MITOSIS; NONHUMAN; ORGANOGENESIS; POLYPLOIDY; PRIORITY JOURNAL; REVIEW; TISSUE GROWTH; TISSUE HOMEOSTASIS; TISSUE REPAIR; UPREGULATION; ANIMAL; APOPTOSIS; CELL DIFFERENTIATION; CELL DIVISION; CELL PROLIFERATION; HUMAN; METABOLISM; PHYSIOLOGY;

MAMMALIA; METAZOA;

ANIMALS; APOPTOSIS; CELL DIFFERENTIATION; CELL DIVISION; CELL PROLIFERATION; HOMEOSTASIS; HUMANS; HYPERTROPHY;

EID: 84897091739     PISSN: 09628924     EISSN: 18793088     Source Type: Journal    
DOI: 10.1016/j.tcb.2013.10.005     Document Type: Review

References (71)

1. Pellettieri J., Alvarado A.S. Cell turnover and adult tissue homeostasis: from humans to planarians. Annu. Rev. Genet. 2007, 41:83-105.
2. Fan Y., Bergmann A. Apoptosis-induced compensatory proliferation. The Cell is dead. Long live the Cell!. Trends Cell Biol. 2008, 18:467-473.
3. Tamori Y., Deng W-M. Tissue repair through cell competition and compensatory cellular hypertrophy in postmitotic epithelia. Dev. Cell 2013, 25:350-363.
4. Losick V.P., et al. Polyploidization and cell fusion contribute to wound healing in the adult Drosophila epithelium. Curr. Biol. 2013, 10.1016/j.cub.2013.09.029.
5. Morata G., et al. Mitogenic signaling from apoptotic cells in Drosophila. Dev. Growth Differ. 2011, 53:168-176.
6. Haynie J.L., Bryant P.J. The effects of X-rays on the proliferation dynamics of cells in the imaginal disc of Drosophila melanagaster. Rouxs Arch. Dev. Biol. 1977, 183:85-100.
7. James A.A., Bryant P.J. A quantitative study of cell death and mitotic inhibition in γ-irradiated imaginal wing discs of Drosophila melanogaster. Radiat. Res. 1981, 87:552-564.
8. Milan M., et al. Developmental parameters of cell death in the wing disc of Drosophila. Proc. Natl. Acad. Sci. U.S.A. 1997, 94:5691-5696.
9. Huh J.R., et al. Compensatory proliferation induced by cell death in the Drosophila wing disc requires activity of the apical cell death caspase Dronc in a nonapoptotic role. Curr. Biol. 2004, 14:1262-1266.
10. Pérez-Garijo A., et al. Caspase inhibition during apoptosis causes abnormal signalling and developmental aberrations in Drosophila. Development 2004, 131:5591-5598.
11. Ryoo H.D., et al. Apoptotic cells can induce compensatory cell proliferation through the JNK and the Wingless signaling pathways. Dev. Cell 2004, 7:491-501.
12. Lee T.V., et al. Drosophila IAP1-mediated ubiquitylation controls activation of the initiator caspase DRONC independent of protein degradation. PLoS Genet. 2011, 7:e1002261.
13. Kondo S., et al. DRONC coordinates cell death and compensatory proliferation. Mol. Cell. Biol. 2006, 26:7258-7268.
14. Smith-Bolton R., et al. Regenerative growth in Drosophila imaginal discs is regulated by Wingless and Myc. Dev. Cell 2009, 16:797-809.
15. V12 and scribbled clones induces tumour growth and invasion. Nature 2010, 463:545-548.
16. Grusche F.A., et al. The Salvador/Warts/Hippo pathway controls regenerative tissue growth in Drosophila melanogaster. Dev. Biol. 2011, 350:255-266.
17. Sun G., Irvine K.D. Regulation of Hippo signaling by Jun kinase signaling during compensatory cell proliferation and regeneration, and in neoplastic tumors. Dev. Biol. 2011, 350:139-151.
18. Pérez-Garijo A., et al. The role of Dpp and Wg in compensatory proliferation and in the formation of hyperplastic overgrowths caused by apoptotic cells in the Drosophila wing disc. Development 2009, 136:1169-1177.
19. Fan Y., Bergmann A. Distinct mechanisms of apoptosis-induced compensatory proliferation in proliferating and differentiating tissues in the Drosophila eye. Dev. Cell 2008, 14:399-410.
20. Calvi B., et al. Cell cycle control of chorion gene amplification. Genes Dev. 1998, 12:734-744.
21. Cavaliere V., et al. dAkt kinase controls follicle cell size during Drosophila oogenesis. Dev. Dyn. 2005, 232:845-854.
22. Hietakangas V., Cohen S.M. Regulation of tissue growth through nutrient sensing. Annu. Rev. Genet. 2009, 43:389-410.
23. Zielke N., et al. Control of Drosophila endocycles by E2F and CRL4(CDT2). Nature 2011, 480:123-127.
24. Duncan A.W. Aneuploidy, polyploidy and ploidy reversal in the liver. Semin. Cell Dev. Biol. 2013, 24:347-356.
25. Duncan A.W., et al. Frequent aneuploidy among normal human hepatocytes. Gastroenterology 2012, 142:25-28.
26. Michalopoulos G.K. Liver regeneration. J. Cell. Physiol. 2007, 213:286-300.
27. Minamishima Y.A., et al. Recovery of liver mass without proliferation of hepatocytes after partial hepatectomy in Skp2-deficient mice. Cancer Res. 2002, 62:995-999.
28. Satyanarayana A., et al. Telomere shortening impairs organ regeneration by inhibiting cell cycle re-entry of a subpopulation of cells. EMBO J. 2003, 22:4003-4013.
29. Miyaoka Y., et al. Hypertrophy and unconventional cell division of hepatocytes underlie liver regeneration. Curr. Biol. 2012, 22:1166-1175.
30. Haga S., et al. Compensatory recovery of liver mass by Akt-mediated hepatocellular hypertrophy in liver-specific STAT3-deficient mice. J. Hepatol. 2005, 43:799-807.
31. Schmucker D.L. Hepatocyte fine structure during maturation and senescence. J. Electron Microsc. Tech. 1990, 14:106-125.
32. Kudryavtsev B.N., et al. Human hepatocyte polyploidization kinetics in the course of life cycle. Virchows Arch. B: Cell Pathol. Incl. Mol. Pathol. 1993, 64:387-393.
33. Joyce N.C. Proliferative capacity of the corneal endothelium. Prog. Retin. Eye Res. 2003, 22:359-389.
34. Mimura T., et al. Corneal endothelial regeneration and tissue engineering. Prog. Retin. Eye Res. 2013, 35:1-17.
35. Roszkowska A.M. Age-related modifications of the corneal endothelium in adults. Int. Ophthalmol. 2004, 25:163-166.
36. Honda H., et al. Cell movements in a living mammalian tissue: long-term observation of individual cells in wounded corneal endothelia of cats. J. Morphol. 1982, 174:25-39.
37. Ikebe H., et al. Changes in nuclear DNA content and cell size of injured human corneal endothelium. Exp. Eye Res. 1988, 47:205-215.
38. Ikebe H., et al. Cytofluorometric nuclear DNA determinations on human corneal endothelial cells. Exp. Eye Res. 1984, 39:497-504.
39. Ikebe H., et al. Age-dependent changes in nuclear DNA content and cell size of presumably normal human corneal endothelium. Exp. Eye Res. 1986, 43:251-258.
40. Blaauw E., et al. Stretch-induced hypertrophy of isolated adult rabbit cardiomyocytes. Am. J. Physiol. Heart Circ. Physiol. 2010, 299:H780-H787.
41. Leychenko A., et al. Stretch-induced hypertrophy activates NFkB-mediated VEGF secretion in adult cardiomyocytes. PLoS ONE 2011, 6:e29055.
42. Sasai N., et al. Involvement of PI3K/Akt/TOR pathway in stretch-induced hypertrophy of myotubes. Muscle Nerve 2010, 41:100-106.
43. Hu B.S., et al. An analysis of the effects of stretch on IGF-I secretion from rat ventricular fibroblasts. Am. J. Physiol. Heart Circ. Physiol. 2007, 293:H677-H683.
44. Unhavaithaya Y., Orr-Weaver T.L. Polyploidization of glia in neural development links tissue growth to blood-brain barrier integrity. Genes Dev. 2012, 26:31-36.
45. Angel P., et al. Function and regulation of AP-1 subunits in skin physiology and pathology. Oncogene 2001, 20:2413-2423.
46. Razzell W., et al. Swatting flies: modelling wound healing and inflammation in Drosophila. Dis. Model Mech. 2011, 4:569-574.
47. Ohsawa S., et al. Mitochondrial defect drives non-autonomous tumour progression through Hippo signalling in Drosophila. Nature 2012, 490:547-551.
48. Enomoto M., Igaki T. Src controls tumorigenesis via JNK-dependent regulation of the Hippo pathway in Drosophila. EMBO Rep. 2013, 14:65-72.
49. Sun G., Irvine K.D. Ajuba family proteins link JNK to Hippo signaling. Sci. Signal. 2013, 6:ra81.
50. Ruohola H., et al. Role of neurogenic genes in establishment of follicle cell fate and oocyte polarity during oogenesis in Drosophila. Cell 1991, 66:433-449.
51. Deng W-M., et al. Notch-Delta signaling induces a transition from mitotic cell cycle to endocycle in Drosophila follicle cells. Development 2001, 128:4737-4746.
52. López-Schier H., St Johnston D. Delta signaling from the germ line controls the proliferation and differentiation of the somatic follicle cells during Drosophila oogenesis. Genes Dev. 2001, 15:1393-1405.
53. Sun J., Deng W-M. Hindsight mediates the role of notch in suppressing hedgehog signaling and cell proliferation. Dev. Cell 2007, 12:431-442.
54. Sun J., Deng W-M. Regulation of the endocycle/gene amplification switch by Notch and ecdysone signaling. J. Cell Biol. 2008, 182:885-896.
55. Polesello C., Tapon N. Salvador-Warts-Hippo signaling promotes Drosophila posterior follicle cell maturation downstream of Notch. Curr. Biol. 2007, 17:1864-1870.
56. Yu J., et al. The Hippo pathway promotes Notch signaling in regulation of cell differentiation, proliferation, and oocyte polarity. PLoS ONE 2008, 3:e1761.
57. Galko M.J., Mark A.K. Cellular and genetic analysis of wound healing in Drosophila larvae. PLoS Biol. 2004, 2:e239.
58. Lecuit T., Le Goff L. Orchestrating size and shape during morphogenesis. Nature 2007, 450:189-192.
59. Weigmann K., et al. Cell cycle progression, growth and patterning in imaginal discs despite inhibition of cell division after inactivation of Drosophila Cdc2 kinase. Development 1997, 124:3555-3563.
60. Neufeld T.P., et al. Coordination of growth and cell division in the Drosophila wing. Cell 1998, 93:1183-1193.
61. Tamori Y., Deng W-M. Cell competition and its implications for development and cancer. J. Genet. Genomics 2011, 38:483-496.
62. Johnston L.A. Competitive interactions between cells: death, growth, and geography. Science 2009, 324:1679-1682.
63. Baker N.E. Cell competition. Curr. Biol. 2011, 21:R11-R15.
64. de Beco S., et al. New frontiers in cell competition. Dev. Dyn. 2012, 241:831-841.
65. Levayer R., Moreno E. Mechanisms of cell competition: Themes and variations. J. Cell Biol. 2013, 200:689-698.
66. Simpson P., Morata G. Differential mitotic rates and patterns of growth in compartments in the Drosophila wing. Dev. Biol. 1981, 85:299-308.
67. de la Cova C., et al. Drosophila myc regulates organ size by inducing cell competition. Cell 2004, 117:107-116.
68. Moreno E., et al. Cells compete for decapentaplegic survival factor to prevent apoptosis in Drosophila wing development. Nature 2002, 416:755-759.
69. Merino M.M., et al. 'Fitness Fingerprints' mediate physiological culling of unwanted neurons in Drosophila. Curr. Biol. 2013, 23:1300-1309.
70. Li W., et al. Merlin/NF2 suppresses tumorigenesis by inhibiting the E3 ubiquitin ligase CRL4(DCAF1) in the nucleus. Cell 2010, 140:477-490.
71. Tamori Y., et al. Involvement of Lgl and Mahjong/VprBP in cell competition. PLoS Biol. 2010, 8:e1000422.