Injury‐induced activation of the MAPK/CREB pathway triggers apoptosis‐induced compensatory proliferation in hydra head regeneration

After bisection, Hydra polyps regenerate their head from the lower half thanks to a head‐organizer activity that is rapidly established at the tip. Head regeneration is also highly plastic as both the wild‐type and the epithelial Hydra (that lack the interstitial cell lineage) can regenerate their head. In the wild‐type context, we previously showed that after mid‐gastric bisection, a large subset of the interstitial cells undergo apoptosis, inducing compensatory proliferation of the surrounding progenitors. This asymmetric process is necessary and sufficient to launch head regeneration. The apoptotic cells transiently release Wnt3, which promotes the formation of a proliferative zone by activating the beta‐catenin pathway in the adjacent cycling cells. However the injury‐induced signaling that triggers apoptosis is unknown. We previously reported an asymmetric immediate activation of the mitogen‐activated protein kinase/ribosomal S6 kinase/cAMP response element binding protein (MAPK/RSK/CREB) pathway in head‐regenerating tips after mid‐gastric bisection. We show here that pharmacological inhibition of the MAPK/ERK pathway or RNAi knockdown of the RSK, CREB, CREB binding protein (CBP) genes prevents apoptosis, compensatory proliferation and blocks head regeneration. As the activation of the MAPK pathway upon injury plays an essential role in regenerating bilaterian species, these results suggest that the MAPK‐dependent activation of apoptosis‐induced compensatory proliferation represents an evolutionary‐conserved mechanism to launch a regenerative process.

[1]  Andreas Bergmann,et al.  Apoptosis, Stem Cells, and Tissue Regeneration , 2010, Science Signaling.

[2]  B. Galliot,et al.  Cell plasticity in homeostasis and regeneration , 2010, Molecular reproduction and development.

[3]  Simona Chera,et al.  The Hydra model: disclosing an apoptosis-driven generator of Wnt-based regeneration. , 2010, Trends in cell biology.

[4]  D. Martinez,et al.  FoxO and Stress Responses in the Cnidarian Hydra vulgaris , 2010, PloS one.

[5]  J. Söding,et al.  The molecular cell death machinery in the simple cnidarian Hydra includes an expanded caspase family and pro- and anti-apoptotic Bcl-2 proteins , 2010, Cell Research.

[6]  G. Longmore,et al.  The Cdc42/Par6/aPKC Polarity Complex Regulates Apoptosis-Induced Compensatory Proliferation in Epithelia , 2010, Current Biology.

[7]  M. Corominas,et al.  Cell death-induced regeneration in wing imaginal discs requires JNK signalling , 2010, Development.

[8]  M. Corominas,et al.  Imaginal discs: Renaissance of a model for regenerative biology , 2010, BioEssays : news and reviews in molecular, cellular and developmental biology.

[9]  A. Böttger,et al.  Apoptosis in pre-Bilaterians: Hydra as a model , 2010, Apoptosis.

[10]  Fang Li,et al.  Apoptotic Cells Activate the “Phoenix Rising” Pathway to Promote Wound Healing and Tissue Regeneration , 2010, Science Signaling.

[11]  D. Green,et al.  Cell death and tissue remodeling in planarian regeneration. , 2010, Developmental biology.

[12]  W. Buzgariu,et al.  Autophagy in Hydra: a response to starvation and stress in early animal evolution. , 2009, Biochimica et biophysica acta.

[13]  J. Martinou,et al.  Apoptotic cells provide an unexpected source of Wnt3 signaling to drive hydra head regeneration. , 2009, Developmental cell.

[14]  I. Hariharan,et al.  Regenerative growth in Drosophila imaginal discs is regulated by Wingless and Myc. , 2009, Developmental cell.

[15]  Oleg Simakov,et al.  Multiple Wnts are involved in Hydra organizer formation and regeneration. , 2009, Developmental biology.

[16]  G. Morata,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 , 2009, Development.

[17]  A. Winoto,et al.  Non‐redundant function of the MEK5–ERK5 pathway in thymocyte apoptosis , 2008, The EMBO journal.

[18]  A. Bergmann,et al.  Distinct mechanisms of apoptosis-induced compensatory proliferation in proliferating and differentiating tissues in the Drosophila eye. , 2008, Developmental cell.

[19]  Ling Wang,et al.  Stress-induced c-Jun Activation Mediated by Polo-like Kinase 3 in Corneal Epithelial Cells* , 2007, Journal of Biological Chemistry.

[20]  N. Satoh,et al.  ERK- and JNK-signalling regulate gene networks that stimulate metamorphosis and apoptosis in tail tissues of ascidian tadpoles , 2007, Development.

[21]  Thomas C G Bosch,et al.  Why polyps regenerate and we don't: towards a cellular and molecular framework for Hydra regeneration. , 2007, Developmental biology.

[22]  M. Miura,et al.  Nonapoptotic functions of caspases: caspases as regulatory molecules for immunity and cell-fate determination. , 2007, Trends in cell biology.

[23]  T. Holstein,et al.  An ancient chordin-like gene in organizer formation of Hydra , 2007, Proceedings of the National Academy of Sciences.

[24]  Brigitte Galliot,et al.  The cAMP response element binding protein (CREB) as an integrative HUB selector in metazoans: Clues from the hydra model system , 2007, Biosyst..

[25]  R. de Rosa,et al.  Hydra, a niche for cell and developmental plasticity. , 2006, Seminars in cell & developmental biology.

[26]  L. Salgado,et al.  Activities of the protein kinases STK, PI3K, MEK, and ERK are required for the development of the head organizer in Hydra magnipapillata. , 2006, Differentiation; research in biological diversity.

[27]  R. de Rosa,et al.  Silencing of the hydra serine protease inhibitor Kazal1 gene mimics the human SPINK1 pancreatic phenotype , 2006, Journal of Cell Science.

[28]  H. Bode,et al.  PI3K and ERK 1‐2 regulate early stages during head regeneration in hydra , 2006, Development, growth & differentiation.

[29]  Yang Luo,et al.  A Splice Variant of Stress Response Gene ATF3 Counteracts NF-κB-dependent Anti-apoptosis through Inhibiting Recruitment of CREB-binding Protein/p300 Coactivator* , 2006, Journal of Biological Chemistry.

[30]  A. Böttger,et al.  Hydra and the Evolution of Apoptosis1 , 2005, Integrative and comparative biology.

[31]  E. Martín-Blanco,et al.  JNK signaling pathway required for wound healing in regenerating Drosophila wing imaginal discs. , 2005, Developmental biology.

[32]  T. Holstein,et al.  HvJNK, a Hydra member of the c-Jun NH2-terminal kinase gene family, is expressed during nematocyte differentiation. , 2005, Gene expression patterns : GEP.

[33]  G. Morata,et al.  Caspase inhibition during apoptosis causes abnormal signalling and developmental aberrations in Drosophila , 2004, Development.

[34]  V. Laudet,et al.  The orphan COUP-TF nuclear receptors are markers for neurogenesis from cnidarians to vertebrates. , 2004, Developmental biology.

[35]  Hyung Don Ryoo,et al.  Apoptotic cells can induce compensatory cell proliferation through the JNK and the Wingless signaling pathways. , 2004, Developmental cell.

[36]  C. Tsilfidis,et al.  Growth and apoptosis during larval forelimb development and adult forelimb regeneration in the newt (Notophthalmus viridescens) , 2004, Development Genes and Evolution.

[37]  Jun R Huh,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 , 2004, Current Biology.

[38]  T. Gojobori,et al.  Detection of apoptosis during planarian regeneration by the expression of apoptosis-related genes and TUNEL assay. , 2004, Gene.

[39]  B. Galliot,et al.  Reactivation of developmental programs: the cAMP-response element-binding protein pathway is involved in hydra head regeneration. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[40]  U. Technau,et al.  Arrested apoptosis of nurse cells during Hydra oogenesis and embryogenesis. , 2003, Developmental biology.

[41]  T. Holstein,et al.  Cnidarians: An evolutionarily conserved model system for regeneration? , 2003, Developmental dynamics : an official publication of the American Association of Anatomists.

[42]  A. Lin Activation of the JNK signaling pathway: Breaking the brake on apoptosis , 2003, BioEssays : news and reviews in molecular, cellular and developmental biology.

[43]  Thomas C G Bosch,et al.  Epithelial interactions in Hydra: apoptosis in interspecies grafts is induced by detachment from the extracellular matrix. , 2002, The Journal of experimental biology.

[44]  M. Miura,et al.  Molecular genetic control of caspases and JNK-mediated neural cell death. , 2002, Archives of histology and cytology.

[45]  Z. Ronai,et al.  An ATF2-derived peptide sensitizes melanomas to apoptosis and inhibits their growth and metastasis. , 2002, The Journal of clinical investigation.

[46]  H. Okano,et al.  Reaper-mediated inhibition of DIAP1-induced DTRAF1 degradation results in activation of JNK in Drosophila , 2002, Nature Cell Biology.

[47]  R. Steele Developmental signaling in Hydra: what does it take to build a "simple" animal? , 2002, Developmental biology.

[48]  Minhong Yan,et al.  Evolution of TNF Signaling Mechanisms JNK-Dependent Apoptosis Triggered by Eiger, the Drosophila Homolog of the TNF Superfamily , 2002, Current Biology.

[49]  A. Leontovich,et al.  Epithelial morphogenesis in hydra requires de novo expression of extracellular matrix components and matrix metalloproteinases. , 2002, Development.

[50]  Marc Montminy,et al.  Transcriptional regulation by the phosphorylation-dependent factor CREB , 2001, Nature Reviews Molecular Cell Biology.

[51]  H. Bode,et al.  Parameters of self-organization in Hydra aggregates. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[52]  Christoph M. Happel,et al.  WNT signalling molecules act in axis formation in the diploblastic metazoan Hydra , 2000, Nature.

[53]  M. Miller,et al.  Oocyte development in Hydra involves selection from competent precursor cells. , 2000, Developmental biology.

[54]  C. David,et al.  Identification of caspases and apoptosis in the simple metazoan Hydra , 1999, Current Biology.

[55]  H. Bode,et al.  HyBra1, a Brachyury homologue, acts during head formation in Hydra. , 1999, Development.

[56]  H. Horvitz,et al.  Genetic control of programmed cell death in the Caenorhabditis elegans hermaphrodite germline. , 1999, Development.

[57]  T. Holstein,et al.  prdl-a, a gene marker for hydra apical differentiation related to triploblastic paired-like head-specific genes. , 1998, Development.

[58]  H. Bode,et al.  Budhead, a fork head/HNF-3 homologue, is expressed during axis formation and head specification in hydra. , 1997, Developmental biology.

[59]  Michael E. Greenberg,et al.  Opposing Effects of ERK and JNK-p38 MAP Kinases on Apoptosis , 1995, Science.

[60]  H. Schaller,et al.  The cAMP response element binding protein is involved in hydra regeneration. , 1995, Development.

[61]  Tsonwin Hai,et al.  ATF3 and ATF3 delta Zip. Transcriptional repression versus activation by alternatively spliced isoforms. , 1994, The Journal of biological chemistry.

[62]  H. Terada,et al.  Genetic analysis of developmental mechanisms in hydra. XVIII. Mechanism for elimination of the interstitial cell lineage in the mutant strain Sf-1. , 1988, Developmental biology.

[63]  T. Bosch,et al.  Growth regulation in Hydra: relationship between epithelial cell cycle length and growth rate. , 1984, Developmental biology.

[64]  T. Fujisawa,et al.  Loss of differentiating nematocytes induced by regeneration and wound healing in Hydra. , 1984, Journal of cell science.

[65]  T Sugiyama,et al.  Genetic analysis of developmental mechanisms in hydra. XII. Analysis of chimaeric hydra produced from a normal and a slow-budding strain (L4). , 1984, Journal of embryology and experimental morphology.

[66]  H. Macwilliams Hydra transplantation phenomena and the mechanism of Hydra head regeneration. II. Properties of the head activation. , 1983, Developmental biology.

[67]  R. D. Campbell,et al.  Tissue economics of hydra: regulation of cell cycle, animal size and development by controlled feeding rates. , 1977, Journal of cell science.

[68]  R. D. Campbell,et al.  Budding in Hydra attenuata: bud stages and fate map. , 1977, The Journal of experimental zoology.

[69]  R. D. Campbell Elimination by Hydra interstitial and nerve cells by means of colchicine. , 1976, Journal of cell science.

[70]  A. Gierer,et al.  Regeneration of hydra from reaggregated cells. , 1972, Nature: New biology.

[71]  Ethel Nicholson Browne,et al.  The production of new hydranths in Hydra by the insertion of small grafts , 1909 .

[72]  W. Buzgariu,et al.  Methods to investigate autophagy during starvation and regeneration in hydra. , 2008, Methods in enzymology.

[73]  M. Levin,et al.  Apoptosis is required during early stages of tail regeneration in Xenopus laevis. , 2007, Developmental biology.

[74]  B. Galliot,et al.  Cnidarians as a model system for understanding evolution and regeneration. , 2002, The International journal of developmental biology.

[75]  T. Bosch,et al.  Role of epithelial cells and programmed cell death in Hydra spermatogenesis. , 2001, Zoology.

[76]  Konstantinos Kaloulis Molecular basis of morphogenetic events in Hydra : study of the CREB and hedgehog pathways during budding and regeneration , 2001 .

[77]  P. Tardent,et al.  Oogenesis in Hydra carnea: A new model based on light and electron microscopic analyses of oocyte and nurse cell differentiation. , 1989, Tissue & cell.

[78]  S. Kondo Altruistic cell suicide in relation to radiation hormesis. , 1988, International journal of radiation biology and related studies in physics, chemistry, and medicine.

[79]  H. Macwilliams Hydra transplantation phenomena and the mechanism of hydra head regeneration. I. Properties of the head inhibition. , 1983, Developmental biology.

[80]  Abraham Trembley Mémoires, pour servir à l'histoire d'un genre de polypes d'eau douce, à bras en forme de cornes , 1975 .

[81]  K. Noda Reconstitution of dissociated cells of hydra , 1971 .