Literature DB >> 16308861

Cellular plasticity in vertebrate regeneration.

Shannon J Odelberg1.   

Abstract

Within the animal kingdom, there are several examples of organisms with remarkable regenerative abilities. Among vertebrates, newts appear to be the most adept at replacing lost structures and injured organs and can regenerate their limbs, tails, spinal cords, jaws, retinas, lenses, optic nerves, intestines, and heart ventricles. This regenerative ability is dependent on the induction of an unusual degree of cellular plasticity near the site of injury. Mature cells lose their differentiated characteristics and revert to proliferating progenitor cells that will later redifferentiate to replace the lost or injured tissues. This degree of cellular plasticity appears to be restricted to those vertebrates with the most remarkable regenerative abilities and is not observed in mammals. However, in the last several years, there have been a few studies suggesting that certain factors present in newt tissues can induce a dedifferentiation response in mammalian cells. These results suggest that the knowledge gained from studying the molecular basis of cellular plasticity in newts and other regeneration-competent model organisms might one day be used to enhance the regenerative potential in mammals. (c) 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 16308861     DOI: 10.1002/ar.b.20080

Source DB:  PubMed          Journal:  Anat Rec B New Anat        ISSN: 1552-4906


  19 in total

1.  Heart of newt: a recipe for regeneration.

Authors:  Bhairab N Singh; Naoko Koyano-Nakagawa; John P Garry; Cyprian V Weaver
Journal:  J Cardiovasc Transl Res       Date:  2010-06-16       Impact factor: 4.132

2.  Blastema cells derived from New Zealand white rabbit's pinna carry stemness properties as shown by differentiation into insulin producing, neural, and osteogenic lineages representing three embryonic germ layers.

Authors:  Morvarid Saeinasab; Maryam M Matin; Fatemeh B Rassouli; Ahmad Reza Bahrami
Journal:  Cytotechnology       Date:  2014-11-05       Impact factor: 2.058

3.  Differential mRNA and tissue expression of lymphangiogenic growth factors (VEGF-C and -D) and their receptor (VEGFR-3) during tail regeneration in a gecko.

Authors:  Helen A Blacker; Sandra Orgeig
Journal:  J Comp Physiol B       Date:  2011-07-29       Impact factor: 2.200

Review 4.  Research proceedings on amphibian model organisms.

Authors:  Lu-Sha Liu; Lan-Ying Zhao; Shou-Hong Wang; Jian-Ping Jiang
Journal:  Dongwuxue Yanjiu       Date:  2016-07-18

Review 5.  miRNA control of tissue repair and regeneration.

Authors:  Chandan K Sen; Subhadip Ghatak
Journal:  Am J Pathol       Date:  2015-06-06       Impact factor: 4.307

6.  Subtractive screen of potential limb regeneration related genes from Pachytriton brevipes.

Authors:  Dan Jiang; Xiao-Long Zhu; Jun-Fang Zhao; Yan-Kuan Zhou; Chao Zhong; Ji Zhang; Xiao Huang
Journal:  Mol Biol Rep       Date:  2014-01-04       Impact factor: 2.316

7.  Activation of pancreatic-duct-derived progenitor cells during pancreas regeneration in adult rats.

Authors:  Wan-Chun Li; J Michael Rukstalis; Wataru Nishimura; Vaja Tchipashvili; Joel F Habener; Arun Sharma; Susan Bonner-Weir
Journal:  J Cell Sci       Date:  2010-07-27       Impact factor: 5.285

8.  Molecular and cellular aspects of amphibian lens regeneration.

Authors:  Jonathan J Henry; Panagiotis A Tsonis
Journal:  Prog Retin Eye Res       Date:  2010-07-16       Impact factor: 21.198

9.  Gene expression profiles of lens regeneration and development in Xenopus laevis.

Authors:  Erica L Malloch; Kimberly J Perry; Lisa Fukui; Verity R Johnson; Jason Wever; Caroline W Beck; Michael W King; Jonathan J Henry
Journal:  Dev Dyn       Date:  2009-09       Impact factor: 3.780

10.  Meningeal cells and glia establish a permissive environment for axon regeneration after spinal cord injury in newts.

Authors:  Katherine A Zukor; David T Kent; Shannon J Odelberg
Journal:  Neural Dev       Date:  2011-01-04       Impact factor: 3.842

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