Literature DB >> 17093139

Is caspase-dependent apoptosis only cell differentiation taken to the extreme?

Pasan Fernando1, Lynn A Megeney.   

Abstract

The benefits of apoptosis for a multicellular organism are obvious and fit the current dogma that the maintenance and viability of such organisms are dependent on the selective elimination of unneeded or deleterious cell types. However, self destruction at the level of the individual cell defies the most basic precepts of biology (sustaining life). If apoptosis is viewed through this construct then one question becomes paramount, i.e., why would an individual cell and its progeny develop, retain, or evolve a mechanism the sole purpose of which is to eliminate itself? In consideration of such a paradox, it is reasonable to postulate that prospective apoptotic pathways coevolved with and or were co-opted from another basic cell function(s) that did not involve the death of the cell per se. In the following article, we present the hypothesis that the conserved biochemical pathways of apoptosis are integral components of terminal cell differentiation and it is the time of engagement and activity level of these pathways that ultimately determines the choice between cell death or cell maturation.

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Year:  2006        PMID: 17093139     DOI: 10.1096/fj.06-5912hyp

Source DB:  PubMed          Journal:  FASEB J        ISSN: 0892-6638            Impact factor:   5.191


  37 in total

1.  High-fat feeding does not induce an autophagic or apoptotic phenotype in female rat skeletal muscle.

Authors:  Troy L Campbell; Andrew S Mitchell; Elliott M McMillan; Darin Bloemberg; Dmytro Pavlov; Isabelle Messa; John G Mielke; Joe Quadrilatero
Journal:  Exp Biol Med (Maywood)       Date:  2014-10-30

Review 2.  Driving apoptosis-relevant proteins toward neural differentiation.

Authors:  Susana Solá; Márcia M Aranha; Cecília M P Rodrigues
Journal:  Mol Neurobiol       Date:  2012-07-01       Impact factor: 5.590

3.  Parole terms for a killer: directing caspase3/CAD induced DNA strand breaks to coordinate changes in gene expression.

Authors:  Brian D Larsen; Lynn A Megeney
Journal:  Cell Cycle       Date:  2010-08-01       Impact factor: 4.534

4.  Insulin-like growth factor receptor-1 and nuclear factor κB are crucial survival signals that regulate caspase-3-mediated lens epithelial cell differentiation initiation.

Authors:  Subhasree Basu; Suren Rajakaruna; A Sue Menko
Journal:  J Biol Chem       Date:  2012-01-24       Impact factor: 5.157

5.  NEU3 sialidase strictly modulates GM3 levels in skeletal myoblasts C2C12 thus favoring their differentiation and protecting them from apoptosis.

Authors:  Luigi Anastasia; Nadia Papini; Francesca Colazzo; Giacomo Palazzolo; Cristina Tringali; Loredana Dileo; Marco Piccoli; Erika Conforti; Clementina Sitzia; Eugenio Monti; Maurilio Sampaolesi; Guido Tettamanti; Bruno Venerando
Journal:  J Biol Chem       Date:  2008-10-22       Impact factor: 5.157

6.  Wnt11 promotes cardiomyocyte development by caspase-mediated suppression of canonical Wnt signals.

Authors:  Mohammad Abdul-Ghani; Daniel Dufort; Rebecca Stiles; Yves De Repentigny; Rashmi Kothary; Lynn A Megeney
Journal:  Mol Cell Biol       Date:  2010-11-01       Impact factor: 4.272

7.  Delay in apoptosome formation attenuates apoptosis in mouse embryonic stem cell differentiation.

Authors:  Shiva Akbari-Birgani; Saman Hosseinkhani; Sepideh Mollamohamadi; Hossein Baharvand
Journal:  J Biol Chem       Date:  2014-04-22       Impact factor: 5.157

8.  Autophagy, apoptosis, and mitochondria: molecular integration and physiological relevance in skeletal muscle.

Authors:  Darin Bloemberg; Joe Quadrilatero
Journal:  Am J Physiol Cell Physiol       Date:  2019-04-24       Impact factor: 4.249

9.  Nuclear Condensation during Mouse Erythropoiesis Requires Caspase-3-Mediated Nuclear Opening.

Authors:  Baobing Zhao; Yang Mei; Matthew J Schipma; Eric Wayne Roth; Reiner Bleher; Joshua Z Rappoport; Amittha Wickrema; Jing Yang; Peng Ji
Journal:  Dev Cell       Date:  2016-03-07       Impact factor: 12.270

10.  N-(4-Hydroxyphenyl) retinamide potentiated paclitaxel for cell cycle arrest and apoptosis in glioblastoma C6 and RG2 cells.

Authors:  Rajiv Janardhanan; Jonathan T Butler; Naren L Banik; Swapan K Ray
Journal:  Brain Res       Date:  2009-03-10       Impact factor: 3.252

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