Calcium-Dependent Neuroepithelial Contractions Expel Damaged Cells from the Developing Brain

Developmental Cell

Volumn 31, Issue 5, 2014, Pages 599-613

  Herrgen, Leah ^a   Voss, Oliver P ^a   Akerman, Colin J ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

MYOSIN ADENOSINE TRIPHOSPHATASE; RHO KINASE; CALCIUM;

ADULT; ANIMAL CELL; APOPTOSIS; ARTICLE; BRAIN DEVELOPMENT; BRAIN VENTRICLE; CALCIUM SIGNALING; CELL DAMAGE; CELL DEATH; CELL NUCLEUS; CELL SHAPE; DISEASE EXACERBATION; ENZYME ACTIVATION; IN VITRO STUDY; IN VIVO STUDY; INFLAMMATION; NEUROEPITHELIUM; NONHUMAN; SCAR FORMATION; STEM CELL; SUPERIOR COLLICULUS; TISSUE INJURY; WOUND HEALING; XENOPUS LAEVIS; ANIMAL; BRAIN; CYTOLOGY; EPITHELIUM; GROWTH, DEVELOPMENT AND AGING; METABOLISM; PATHOLOGY; PHYSIOLOGY;

MAMMALIA; XENOPUS LAEVIS;

ACTOMYOSIN; ANIMALS; BRAIN; CALCIUM; CELL DEATH; EPITHELIUM; WOUND HEALING; XENOPUS LAEVIS;

EID: 84918534316     PISSN: 15345807     EISSN: 18781551     Source Type: Journal    
DOI: 10.1016/j.devcel.2014.10.012     Document Type: Article

References (53)

1. Abbracchio M.P., Burnstock G., Boeynaems J.-M., Barnard E.A., Boyer J.L., Kennedy C., Knight G.E., Fumagalli M., Gachet C., Jacobson K.A., Weisman G.A. International Union of Pharmacology LVIII: update on the P2Y G protein-coupled nucleotide receptors: from molecular mechanisms and pathophysiology to therapy. Pharmacol. Rev. 2006, 58:281-341.
2. Andrade D., Rosenblatt J. Apoptotic regulation of epithelial cellular extrusion. Apoptosis 2011, 16:491-501.
3. Baethmann M., Kahn T., Lenard H.G., Voit T. Fetal CNS damage after exposure to maternal trauma during pregnancy. Acta Paediatr. 1996, 85:1331-1338.
4. Bement W.M., Forscher P., Mooseker M.S. A novel cytoskeletal structure involved in purse string wound closure and cell polarity maintenance. J.Cell Biol. 1993, 121:565-578.
5. Bement W.M., Mandato C.A., Kirsch M.N. Wound-induced assembly and closure of an actomyosin purse string in Xenopus oocytes. Curr. Biol. 1999, 9:579-587.
6. Benink H.A., Bement W.M. Concentric zones of active RhoA and Cdc42 around single cell wounds. J.Cell Biol. 2005, 168:429-439.
7. Bielefeld K.A., Amini-Nik S., Alman B.A. Cutaneous wound healing: recruiting developmental pathways for regeneration. Cell. Mol. Life Sci. 2013, 70:2059-2081.
8. Burkel B.M., von Dassow G., Bement W.M. Versatile fluorescent probes for actin filaments based on the actin-binding domain of utrophin. Cell Motil. Cytoskeleton 2007, 64:822-832.
9. Clark A.G., Miller A.L., Vaughan E., Yu H.-Y.E., Penkert R., Bement W.M. Integration of single and multicellular wound responses. Curr. Biol. 2009, 19:1389-1395.
10. Cordeiro J.V., Jacinto A. The role of transcription-independent damage signals in the initiation of epithelial wound healing. Nat. Rev. Mol. Cell Biol. 2013, 14:249-262.
11. Corrigall D., Walther R.F., Rodriguez L., Fichelson P., Pichaud F. Hedgehog signaling is a principal inducer of Myosin-II-driven cell ingression in Drosophila epithelia. Dev. Cell 2007, 13:730-742.
12. Crosby L.M., Waters C.M. Epithelial repair mechanisms in the lung. Am. J. Physiol. Lung Cell. Mol. Physiol. 2010, 298:L715-L731.
13. Degen K.E., Gourdie R.G. Embryonic wound healing: a primer for engineering novel therapies for tissue repair. Birth Defects Res. C Embryo Today 2012, 96:258-270.
14. Gu Y., Forostyan T., Sabbadini R., Rosenblatt J. Epithelial cell extrusion requires the sphingosine-1-phosphate receptor 2 pathway. J.Cell Biol. 2011, 193:667-676.
15. Gurtner G.C., Werner S., Barrandon Y., Longaker M.T. Wound repair and regeneration. Nature 2008, 453:314-321.
16. Halfter W. Effect of wound healing and tissue transplantation on thenavigation of axons in organ-cultured embryonic chick eyes. J.Comp. Neurol. 1993, 327:442-457.
17. Hayes B., Ryan S., Stephenson J.B.P., King M.D. Cerebral palsy after maternal trauma in pregnancy. Dev. Med. Child Neurol. 2007, 49:700-706.
18. Joshi S.D., von Dassow M., Davidson L.A. Experimental control of excitable embryonic tissues: three stimuli induce rapid epithelial contraction. Exp. Cell Res. 2010, 316:103-114.
19. Khakh B.S., Burnstock G., Kennedy C., King B.F., North R.A., Séguéla P., Voigt M., Humphrey P.P. International union of pharmacology. XXIV. Current status of the nomenclature and properties of P2X receptors and their subunits. Pharmacol. Rev. 2001, 53:107-118.
20. Kroemer G., Galluzzi L., Vandenabeele P., Abrams J., Alnemri E.S., Baehrecke E.H., Blagosklonny M.V., El-Deiry W.S., Golstein P., Green D.R., et al. Classification of cell death: recommendations of the Nomenclature Committee on Cell Death 2009. Cell Death Differ. 2009, 16:3-11. Nomenclature Committee on Cell Death 2009.
21. Krysko D.V., D'Herde K., Vandenabeele P. Clearance ofapoptotic and necrotic cells and its immunological consequences. Apoptosis 2006, 11:1709-1726.
22. Larson B.J., Longaker M.T., Lorenz H.P. Scarless fetal wound healing: a basic science review. Plast. Reconstr. Surg. 2010, 126:1172-1180.
23. Lawson A., England M.A. Studies on wound healing in the neuroepithelium of the chick embryo. Anat. Rec. 1992, 233:291-300.
24. Lawson A., England M.A. The effect of embryonic cerebrospinal fluid pressure and morphogenetic brain expansion on wound healing in the midbrain of the chick embryo. Anat. Embryol. (Berl.) 1996, 193:601-610.
25. Lázár G. The development of the optic tectum in Xenopus laevis: a Golgi study. J.Anat. 1973, 116:347-355.
26. Leroy-Malherbe V., Bonnier C., Papiernik E., Groos E., Landrieu P. The association between developmental handicaps and traumatic brain injury during pregnancy: an issue that deserves more systematic evaluation. Brain Inj. 2006, 20:1355-1365.
27. Liu X., Hashimoto-Torii K., Torii M., Ding C., Rakic P. Gap junctions/hemichannels modulate interkinetic nuclear migration in the forebrain precursors. J.Neurosci. 2010, 30:4197-4209.
28. Lo D.D., Zimmermann A.S., Nauta A., Longaker M.T., Lorenz H.P. Scarless fetal skin wound healing update. Birth Defects Res. C Embryo Today 2012, 96:237-247.
29. Martin P., Lewis J. Actin cables and epidermal movement in embryonic wound healing. Nature 1992, 360:179-183.
30. Martin P., Leibovich S.J. Inflammatory cells during wound repair: the good, the bad and the ugly. Trends Cell Biol. 2005, 15:599-607.
31. Martin A.C., Kaschube M., Wieschaus E.F. Pulsed contractions of an actin-myosin network drive apical constriction. Nature 2009, 457:495-499.
32. McCluskey J., Martin P. Analysis of the tissue movements of embryonic wound healing-DiI studies in the limb bud stage mouse embryo. Dev. Biol. 1995, 170:102-114.
33. Naik-Mathuria B., Gay A.N., Zhu X., Yu L., Cass D.L., Olutoye O.O. Age-dependent recruitment of neutrophils by fetal endothelial cells: implications in scarless wound healing. J.Pediatr. Surg. 2007, 42:166-171.
34. Nieuwkoop P.D., Faber J. Normal Table of Xenopus laevis (Daudin) 1994, Garland Publishing, New York.
35. Novo E., Parola M. Redox mechanisms in hepatic chronic wound healing and fibrogenesis. Fibrogenesis Tissue Repair 2008, 1:5.
36. Pearson R.A., Dale N., Llaudet E., Mobbs P. ATP released viagap junction hemichannels from the pigment epithelium regulates neural retinal progenitor proliferation. Neuron 2005, 46:731-744.
37. Rauzi M., Lenne P.-F., Lecuit T. Planar polarized actomyosin contractile flows control epithelial junction remodelling. Nature 2010, 468:1110-1114.
38. Razzell W., Evans I.R., Martin P., Wood W. Calcium flashes orchestrate the wound inflammatory response through DUOX activation and hydrogen peroxide release. Curr. Biol. 2013, 23:424-429.
39. Riento K., Ridley A.J. Rocks: multifunctional kinases in cell behaviour. Nat. Rev. Mol. Cell Biol. 2003, 4:446-456.
40. Rosenblatt J., Raff M.C., Cramer L.P. An epithelial cell destined for apoptosis signals its neighbors to extrude it by an actin- and myosin-dependent mechanism. Curr. Biol. 2001, 11:1847-1857.
41. Sauer F.C. Mitosis in the neural tube. J.Comp. Neurol. 1935, 62:377-405.
42. Sauzeau V., Le Jeune H., Cario-Toumaniantz C., Vaillant N., Gadeau A.P., Desgranges C., Scalbert E., Chardin P., Pacaud P., Loirand G. P2Y(1), P2Y(2), P2Y(4), and P2Y(6) receptors are coupled to Rho and Rho kinase activation in vascular myocytes. Am. J. Physiol. Heart Circ. Physiol. 2000, 278:H1751-H1761.
43. Sherrard K., Robin F., Lemaire P., Munro E. Sequential activation of apical and basolateral contractility drives ascidian endoderm invagination. Curr. Biol. 2010, 20:1499-1510.
44. Sieger D., Moritz C., Ziegenhals T., Prykhozhij S., Peri F. Long-range Ca2+ waves transmit brain-damage signals to microglia. Dev. Cell 2012, 22:1138-1148.
45. Siehler S. Regulation of RhoGEF proteins by G12/13-coupled receptors. Br. J. Pharmacol. 2009, 158:41-49.
46. Singer A.J., Clark R.A. Cutaneous wound healing. N.Engl. J. Med. 1999, 341:738-746.
47. Sonnemann K.J., Bement W.M. Wound repair: toward understanding and integration of single-cell and multicellular wound responses. Annu. Rev. Cell Dev. Biol. 2011, 27:237-263.
48. Soto X., Li J., Lea R., Dubaissi E., Papalopulu N., Amaya E. Inositol kinase and its product accelerate wound healing by modulating calcium levels, Rho GTPases, and F-actin assembly. Proc. Natl. Acad. Sci. USA 2013, 110:11029-11034.
49. Straight A.F., Cheung A., Limouze J., Chen I., Westwood N.J., Sellers J.R., Mitchison T.J. Dissecting temporal and spatial control of cytokinesis with a myosin II Inhibitor. Science 2003, 299:1743-1747.
50. Straznicky K., Gaze R.M. The development of the tectum in Xenopus laevis: an autoradiographic study. J.Embryol. Exp. Morphol. 1972, 28:87-115.
51. Wallingford J.B., Ewald A.J., Harland R.M., Fraser S.E. Calcium signaling during convergent extension in Xenopus. Curr. Biol. 2001, 11:652-661.
52. Weissman T.A., Riquelme P.A., Ivic L., Flint A.C., Kriegstein A.R. Calcium waves propagate through radial glial cells and modulate proliferation in the developing neocortex. Neuron 2004, 43:647-661.
53. Whitby D.J., Longaker M.T., Harrison M.R., Adzick N.S., Ferguson M.W. Rapid epithelialisation of fetal wounds is associated with the early deposition of tenascin. J.Cell Sci. 1991, 99:583-586.