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Genetic Models of Apoptosis-Induced Proliferation Decipher Activation of JNK and Identify a Requirement of EGFR Signaling for Tissue Regenerative Responses in
Recent work in several model organisms has revealed that apoptotic cells are able to stimulate neighboring surviving cells to undergo additional proliferation, a phenomenon termed apoptosis-induced proliferation. This process depends critically on apoptotic caspases such as Dronc, the Caspase-9 ortholog in Drosophila, and may have important implications for tumorigenesis. While it is known that Dronc can induce the activity of Jun N-terminal kinase (JNK) for apoptosis-induced proliferation, the mechanistic details of this activation are largely unknown. It is also controversial if JNK activity occurs in dying or in surviving cells. Signaling molecules of the Wnt and BMP families have been implicated in apoptosis-induced proliferation, but it is unclear if they are the only ones. To address these questions, we have developed an efficient assay for screening and identification of genes that regulate or mediate apoptosis-induced proliferation. We have identified a subset of genes acting upstream of JNK activity including Rho1. We also demonstrate that JNK activation occurs both in apoptotic cells as well as in neighboring surviving cells. In a genetic screen, we identified signaling by the EGFR pathway as important for apoptosis-induced proliferation acting downstream of JNK signaling. These data underscore the importance of genetic screening and promise an improved understanding of the mechanisms of apoptosis-induced proliferation.
Vyšlo v časopise: Genetic Models of Apoptosis-Induced Proliferation Decipher Activation of JNK and Identify a Requirement of EGFR Signaling for Tissue Regenerative Responses in. PLoS Genet 10(1): e32767. doi:10.1371/journal.pgen.1004131
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1004131Souhrn
Recent work in several model organisms has revealed that apoptotic cells are able to stimulate neighboring surviving cells to undergo additional proliferation, a phenomenon termed apoptosis-induced proliferation. This process depends critically on apoptotic caspases such as Dronc, the Caspase-9 ortholog in Drosophila, and may have important implications for tumorigenesis. While it is known that Dronc can induce the activity of Jun N-terminal kinase (JNK) for apoptosis-induced proliferation, the mechanistic details of this activation are largely unknown. It is also controversial if JNK activity occurs in dying or in surviving cells. Signaling molecules of the Wnt and BMP families have been implicated in apoptosis-induced proliferation, but it is unclear if they are the only ones. To address these questions, we have developed an efficient assay for screening and identification of genes that regulate or mediate apoptosis-induced proliferation. We have identified a subset of genes acting upstream of JNK activity including Rho1. We also demonstrate that JNK activation occurs both in apoptotic cells as well as in neighboring surviving cells. In a genetic screen, we identified signaling by the EGFR pathway as important for apoptosis-induced proliferation acting downstream of JNK signaling. These data underscore the importance of genetic screening and promise an improved understanding of the mechanisms of apoptosis-induced proliferation.
Zdroje
1. ThompsonCB (1995) Apoptosis in the pathogenesis and treatment of disease. Science 267 : 1456–1462.
2. KumarS (2007) Caspase function in programmed cell death. Cell Death Differ 14 : 32–43.
3. BaoQ, ShiY (2007) Apoptosome: a platform for the activation of initiator caspases. Cell Death Differ 14 : 56–65.
4. DorstynL, ColussiPA, QuinnLM, RichardsonH, KumarS (1999) DRONC, an ecdysone-inducible Drosophila caspase. Proc Natl Acad Sci U S A 96 : 4307–4312.
5. FraserAG, McCarthyNJ, EvanGI (1997) drICE is an essential caspase required for apoptotic activity in Drosophila cells. Embo J 16 : 6192–6199.
6. SongZ, McCallK, StellerH (1997) DCP-1, a Drosophila cell death protease essential for development. Science 275 : 536–540.
7. XuD, LiY, ArcaroM, LackeyM, BergmannA (2005) The CARD-carrying caspase Dronc is essential for most, but not all, developmental cell death in Drosophila. Development 132 : 2125–2134.
8. XuD, WangY, WilleckeR, ChenZ, DingT, et al. (2006) The effector caspases drICE and dcp-1 have partially overlapping functions in the apoptotic pathway in Drosophila. Cell Death Differ 13 : 1697–1706.
9. ChewSK, AkdemirF, ChenP, LuWJ, MillsK, et al. (2004) The apical caspase dronc governs programmed and unprogrammed cell death in Drosophila. Dev Cell 7 : 897–907.
10. DaishTJ, MillsK, KumarS (2004) Drosophila caspase DRONC is required for specific developmental cell death pathways and stress-induced apoptosis. Dev Cell 7 : 909–915.
11. MuroI, BerryDL, HuhJR, ChenCH, HuangH, et al. (2006) The Drosophila caspase Ice is important for many apoptotic cell deaths and for spermatid individualization, a nonapoptotic process. Development 133 : 3305–3315.
12. KondoS, Senoo-MatsudaN, HiromiY, MiuraM (2006) DRONC coordinates cell death and compensatory proliferation. Mol Cell Biol 26 : 7258–7268.
13. VauxDL, SilkeJ (2005) IAPs, RINGs and ubiquitylation. Nat Rev Mol Cell Biol 6 : 287–297.
14. MeierP, SilkeJ, LeeversSJ, EvanGI (2000) The Drosophila caspase DRONC is regulated by DIAP1. Embo J 19 : 598–611.
15. ZachariouA, TenevT, GoyalL, AgapiteJ, StellerH, et al. (2003) IAP-antagonists exhibit non-redundant modes of action through differential DIAP1 binding. Embo J 22 : 6642–6652.
16. WhiteK, GretherME, AbramsJM, YoungL, FarrellK, et al. (1994) Genetic control of programmed cell death in Drosophila. Science 264 : 677–683.
17. GretherME, AbramsJM, AgapiteJ, WhiteK, StellerH (1995) The head involution defective gene of Drosophila melanogaster functions in programmed cell death. Genes Dev 9 : 1694–1708.
18. ChenP, NordstromW, GishB, AbramsJM (1996) grim, a novel cell death gene in Drosophila. Genes Dev 10 : 1773–1782.
19. HaysR, WicklineL, CaganR (2002) Morgue mediates apoptosis in the Drosophila melanogaster retina by promoting degradation of DIAP1. Nat Cell Biol 4 : 425–431.
20. HolleyCL, OlsonMR, Colon-RamosDA, KornbluthS (2002) Reaper eliminates IAP proteins through stimulated IAP degradation and generalized translational inhibition. Nat Cell Biol 4 : 439–444.
21. RyooHD, BergmannA, GonenH, CiechanoverA, StellerH (2002) Regulation of Drosophila IAP1 degradation and apoptosis by reaper and ubcD1. Nat Cell Biol 4 : 432–438.
22. WingJP, SchreaderBA, YokokuraT, WangY, AndrewsPS, et al. (2002) Drosophila Morgue is an F box/ubiquitin conjugase domain protein important for grim-reaper mediated apoptosis. Nat Cell Biol 4 : 451–456.
23. YooSJ, HuhJR, MuroI, YuH, WangL, et al. (2002) Hid, Rpr and Grim negatively regulate DIAP1 levels through distinct mechanisms. Nat Cell Biol 4 : 416–424.
24. HaynieJL, BryantPJ (1977) The effects of X-rays on the proliferation dynamics of cells in the imaginal disc of Drosophila melanogaster. Rouxs Arch Dev Biol 183 : 85–100.
25. Perez-GarijoA, MartinFA, MorataG (2004) Caspase inhibition during apoptosis causes abnormal signalling and developmental aberrations in Drosophila. Development 131 : 5591–5598.
26. Perez-GarijoA, ShlevkovE, MorataG (2009) 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 136 : 1169–1177.
27. RyooHD, GorencT, StellerH (2004) Apoptotic cells can induce compensatory cell proliferation through the JNK and the Wingless signaling pathways. Dev Cell 7 : 491–501.
28. HuhJR, GuoM, HayBA (2004) 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 14 : 1262–1266.
29. FanY, BergmannA (2008) Distinct mechanisms of apoptosis-induced compensatory proliferation in proliferating and differentiating tissues in the Drosophila eye. Dev Cell 14 : 399–410.
30. CheraS, GhilaL, DobretzK, WengerY, BauerC, et al. (2009) Apoptotic cells provide an unexpected source of Wnt3 signaling to drive hydra head regeneration. Dev Cell 17 : 279–289.
31. TsengAS, AdamsDS, QiuD, KoustubhanP, LevinM (2007) Apoptosis is required during early stages of tail regeneration in Xenopus laevis. Dev Biol 301 : 62–69.
32. PellettieriJ, FitzgeraldP, WatanabeS, MancusoJ, GreenDR, et al. (2010) Cell death and tissue remodeling in planarian regeneration. Dev Biol 338 : 76–85.
33. PellettieriJ, Sanchez AlvaradoA (2007) Cell turnover and adult tissue homeostasis: from humans to planarians. Annu Rev Genet 41 : 83–105.
34. VlaskalinT, WongCJ, TsilfidisC (2004) Growth and apoptosis during larval forelimb development and adult forelimb regeneration in the newt (Notophthalmus viridescens). Dev Genes Evol 214 : 423–431.
35. LiF, HuangQ, ChenJ, PengY, RoopDR, et al. (2010) Apoptotic cells activate the “phoenix rising” pathway to promote wound healing and tissue regeneration. Sci Signal 3: ra13.
36. FanY, BergmannA (2008) Apoptosis-induced compensatory proliferation. The Cell is dead. Long live the Cell! Trends Cell Biol 18 : 467–473.
37. BergmannA, StellerH (2010) Apoptosis, stem cells, and tissue regeneration. Science Signaling 3: re8.
38. RyooHD, BergmannA (2012) The role of apoptosis-induced proliferation for regeneration and cancer. Cold Spring Harb Perspect Biol 4: a008797.
39. MollereauB, Perez-GarijoA, BergmannA, MiuraM, GerlitzO, et al. (2013) Compensatory proliferation and apoptosis-induced proliferation: A need for clarification. Cell Death Differ 20 (1) 181.
40. HawkinsCJ, YooSJ, PetersonEP, WangSL, VernooySY, et al. (2000) The Drosophila caspase DRONC cleaves following glutamate or aspartate and is regulated by DIAP1, HID, and GRIM. J Biol Chem 275 : 27084–27093.
41. ClemRJ, FechheimerM, MillerLK (1991) Prevention of apoptosis by a baculovirus gene during infection of insect cells. Science 254 : 1388–1390.
42. Smith-BoltonRK, WorleyMI, KandaH, HariharanIK (2009) Regenerative growth in Drosophila imaginal discs is regulated by Wingless and Myc. Dev Cell 16 : 797–809.
43. BergantinosC, CorominasM, SerrasF (2010) Cell death-induced regeneration in wing imaginal discs requires JNK signalling. Development 137 : 1169–1179.
44. HerreraSC, MartinR, MorataG (2013) Tissue homeostasis in the wing disc of Drosophila melanogaster: immediate response to massive damage during development. PLoS Genet 9: e1003446.
45. Ryoo HD, Bergmann A (2012) The role of apoptosis-induced proliferation for regeneration and cancer. In: Cell Survival and Cell Death EH Baehrecke, DR Green, S Kornbluth and G Salvesen Eds, Cold Spring Harbor Press, Cold Spring Harbor, NY
46. WellsBS, YoshidaE, JohnstonLA (2006) Compensatory proliferation in Drosophila imaginal discs requires Dronc-dependent p53 activity. Curr Biol 16 : 1606–1615.
47. WellsBS, JohnstonLA (2012) Maintenance of imaginal disc plasticity and regenerative potential in Drosophila by p53. Dev Biol 361 : 263–276.
48. ShlevkovE, MorataG (2012) A dp53/JNK-dependant feedback amplification loop is essential for the apoptotic response to stress in Drosophila. Cell Death Differ 19 : 451–460.
49. SuissaY, ZivO, DinurT, AramaE, GerlitzO (2011) The NAB-Brk signal bifurcates at JNK to independently induce apoptosis and compensatory proliferation. J Biol Chem 286 : 15556–15564.
50. UhlirovaM, JasperH, BohmannD (2005) Non-cell-autonomous induction of tissue overgrowth by JNK/Ras cooperation in a Drosophila tumor model. Proc Natl Acad Sci U S A 102 : 13123–13128.
51. WarnerSJ, YashiroH, LongmoreGD (2010) The Cdc42/Par6/aPKC polarity complex regulates apoptosis-induced compensatory proliferation in epithelia. Curr Biol 20 : 677–686.
52. IgakiT (2009) Correcting developmental errors by apoptosis: lessons from Drosophila JNK signaling. Apoptosis 14 : 1021–1028.
53. WestonCR, DavisRJ (2007) The JNK signal transduction pathway. Curr Opin Cell Biol 19 : 142–149.
54. SunG, IrvineKD (2011) Regulation of Hippo signaling by Jun kinase signaling during compensatory cell proliferation and regeneration, and in neoplastic tumors. Dev Biol 350 : 139–151.
55. SunG, IrvineKD (2013) Ajuba family proteins link JNK to Hippo signaling. Sci Signal 6: ra81.
56. ChenL, ParkSM, TumanovAV, HauA, SawadaK, et al. (2010) CD95 promotes tumour growth. Nature 465 : 492–496.
57. HalderG, CallaertsP, FlisterS, WalldorfU, KloterU, et al. (1998) Eyeless initiates the expression of both sine oculis and eyes absent during Drosophila compound eye development. Development 125 : 2181–2191.
58. LegentK, TreismanJE (2008) Wingless signaling in Drosophila eye development. Methods Mol Biol 469 : 141–161.
59. ChatterjeeN, BohmannD (2012) A versatile PhiC31 based reporter system for measuring AP-1 and Nrf2 signaling in Drosophila and in tissue culture. PLoS One 7: e34063.
60. RudrapatnaVA, BangiE, CaganRL (2013) Caspase signalling in the absence of apoptosis drives Jnk-dependent invasion. EMBO Rep 14 : 172–177.
61. BoutrosM, AgaisseH, PerrimonN (2002) Sequential activation of signaling pathways during innate immune responses in Drosophila. Dev Cell 3 : 711–722.
62. GeukingP, NarasimamurthyR, LemaitreB, BaslerK, LeulierF (2009) A non-redundant role for Drosophila Mkk4 and hemipterous/Mkk7 in TAK1-mediated activation of JNK. PLoS One 4: e7709.
63. NeischAL, SpeckO, StronachB, FehonRG (2010) Rho1 regulates apoptosis via activation of the JNK signaling pathway at the plasma membrane. J Cell Biol 189 : 311–323.
64. BrumbyAM, GouldingKR, SchlosserT, LoiS, GaleaR, et al. (2011) Identification of novel Ras-cooperating oncogenes in Drosophila melanogaster: a RhoGEF/Rho-family/JNK pathway is a central driver of tumorigenesis. Genetics 188 : 105–125.
65. KhooP, AllanK, WilloughbyL, BrumbyAM, RichardsonHE (2013) In Drosophila, RhoGEF2 cooperates with activated Ras in tumorigenesis through a pathway involving Rho1-Rok-Myosin-II and JNK signalling. Dis Model Mech 6 : 661–678.
66. RudrapatnaVA, BangiE, CaganRL (2013) A Jnk-Rho-Actin remodeling positive feedback network directs Src-driven invasion. Oncogene [epub ahead of print].
67. WuY, BrockAR, WangY, FujitaniK, UedaR, et al. (2009) A blood-borne PDGF/VEGF-like ligand initiates wound-induced epidermal cell migration in Drosophila larvae. Curr Biol 19 : 1473–1477.
68. BabcockDT, LandryC, GalkoMJ (2009) Cytokine signaling mediates UV-induced nociceptive sensitization in Drosophila larvae. Curr Biol 19 : 799–806.
69. LeschC, JoJ, WuY, FishGS, GalkoMJ (2010) A targeted UAS-RNAi screen in Drosophila larvae identifies wound closure genes regulating distinct cellular processes. Genetics 186 : 943–957.
70. FanY, BergmannA (2010) The cleaved-Caspase-3 antibody is a marker of Caspase-9-like DRONC activity in Drosophila. Cell Death Differ 17 : 534–539.
71. MorenoE, YanM, BaslerK (2002) Evolution of TNF signaling mechanisms: JNK-dependent apoptosis triggered by Eiger, the Drosophila homolog of the TNF superfamily. Curr Biol 12 : 1263–1268.
72. IgakiT, KandaH, Yamamoto-GotoY, KanukaH, KuranagaE, et al. (2002) Eiger, a TNF superfamily ligand that triggers the Drosophila JNK pathway. Embo J 21 : 3009–3018.
73. XueL, IgakiT, KuranagaE, KandaH, MiuraM, et al. (2007) Tumor suppressor CYLD regulates JNK-induced cell death in Drosophila. Dev Cell 13 : 446–454.
74. RutledgeBJ, ZhangK, BierE, JanYN, PerrimonN (1992) The Drosophila spitz gene encodes a putative EGF-like growth factor involved in dorsal-ventral axis formation and neurogenesis. Genes Dev 6 : 1503–1517.
75. SpradlingAC, SternD, BeatonA, RhemEJ, LavertyT, et al. (1999) The Berkeley Drosophila Genome Project gene disruption project: Single P-element insertions mutating 25% of vital Drosophila genes. Genetics 153 : 135–177.
76. MusacchioM, PerrimonN (1996) The Drosophila kekkon genes: novel members of both the leucine-rich repeat and immunoglobulin superfamilies expressed in the CNS. Dev Biol 178 : 63–76.
77. MorrisonCM, HalderG (2010) Characterization of a dorsal-eye Gal4 Line in Drosophila. Genesis 48 : 3–7.
78. McGuireSE, LePT, OsbornAJ, MatsumotoK, DavisRL (2003) Spatiotemporal rescue of memory dysfunction in Drosophila. Science 302 : 1765–1768.
79. TioM, MaC, MosesK (1994) spitz, a Drosophila homolog of transforming growth factor-alpha, is required in the founding photoreceptor cells of the compound eye facets. Mech Dev 48 : 13–23.
80. FreemanM (1994) The spitz gene is required for photoreceptor determination in the Drosophila eye where it interacts with the EGF receptor. Mech Dev 48 : 25–33.
81. KurokawaH, NishioK, FukumotoH, TomonariA, SuzukiT, et al. (1999) Alteration of caspase-3 (CPP32/Yama/apopain) in wild-type MCF-7, breast cancer cells. Oncol Rep 6 : 33–37.
82. DevarajanE, SahinAA, ChenJS, KrishnamurthyRR, AggarwalN, et al. (2002) Down-regulation of caspase 3 in breast cancer: a possible mechanism for chemoresistance. Oncogene 21 : 8843–8851.
83. IolasconA, BorrielloA, GiordaniL, CucciollaV, MorettiA, et al. (2003) Caspase 3 and 8 deficiency in human neuroblastoma. Cancer Genet Cytogenet 146 : 41–47.
84. GhavamiS, HashemiM, AndeSR, YeganehB, XiaoW, et al. (2009) Apoptosis and cancer: mutations within caspase genes. J Med Genet 46 : 497–510.
85. SnipasSJ, DragM, StennickeHR, SalvesenGS (2008) Activation mechanism and substrate specificity of the Drosophila initiator caspase DRONC. Cell Death Differ 15 : 938–945.
86. IrvineKD (2012) Integration of intercellular signaling through the Hippo pathway. Semin Cell Dev Biol 23 (7) 812–7.
87. HalderG, JohnsonRL (2011) Hippo signaling: growth control and beyond. Development 138 : 9–22.
88. LiQ, LiuDW, ZhangLM, ZhuB, HeYT, et al. (2005) Effects of augmentation of liver regeneration recombinant plasmid on rat hepatic fibrosis. World J Gastroenterol 11 : 2438–2443.
89. PawlowskiR, JuraJ (2006) ALR and liver regeneration. Mol Cell Biochem 288 : 159–169.
90. CheraS, GhilaL, WengerY, GalliotB (2011) Injury-induced activation of the MAPK/CREB pathway triggers apoptosis-induced compensatory proliferation in hydra head regeneration. Dev Growth Differ 53 : 186–201.
91. BergmannA, AgapiteJ, McCallK, StellerH (1998) The Drosophila gene hid is a direct molecular target of Ras-dependent survival signaling. Cell 95 : 331–341.
92. KuradaP, WhiteK (1998) Ras promotes cell survival in Drosophila by downregulating hid expression. Cell 95 : 319–329.
93. GerholdAR, RichterDJ, YuAS, HariharanIK (2011) Identification and characterization of genes required for compensatory growth in Drosophila. Genetics 189 : 1309–1326.
94. HuangQ, LiF, LiuX, LiW, ShiW, et al. (2011) Caspase 3-mediated stimulation of tumor cell repopulation during cancer radiotherapy. Nat Med 17 : 860–866.
Štítky
Genetika Reprodukčná medicína
Článek Unwrapping BacteriaČlánek A Chaperone-Assisted Degradation Pathway Targets Kinetochore Proteins to Ensure Genome StabilityČlánek The Candidate Splicing Factor Sfswap Regulates Growth and Patterning of Inner Ear Sensory OrgansČlánek The SPF27 Homologue Num1 Connects Splicing and Kinesin 1-Dependent Cytoplasmic Trafficking inČlánek Down-Regulation of eIF4GII by miR-520c-3p Represses Diffuse Large B Cell Lymphoma DevelopmentČlánek Meta-Analysis Identifies Gene-by-Environment Interactions as Demonstrated in a Study of 4,965 MiceČlánek High Risk Population Isolate Reveals Low Frequency Variants Predisposing to Intracranial Aneurysms
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