Literature DB >> 11059808

One path to cell death in the nervous system.

J Glasgow1, R Perez-Polo.   

Abstract

Both acute and chronic insults to the nervous system can result in changes in homeostasis that result in cell death or recovery processes that alter function. The signaling mechanisms for this broad spectrum of events that impair neurological function span the gamut from abrupt injury to the slow onset of neurodegenerative diseases in extreme aging. A common element in all of these events is the triggering of signal cascades that determine cellular commitment to apoptosis as a ameliorative alternative to inflammatory necrosis. Key in these cascades is the activation of the caspase and Bcl-family of proteins by the NF-kappaB transcription factor. Here we consider aspects of specificity of activation as a result of the differential expression of NF-kappaB proteins and their regulation of selective genes as a result of binding to select DNA consensus sequences out of the 64 different combinations that constitute the NF-kappaB DNA binding consensus sequence.

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Year:  2000        PMID: 11059808     DOI: 10.1023/a:1007612716591

Source DB:  PubMed          Journal:  Neurochem Res        ISSN: 0364-3190            Impact factor:   3.996


  147 in total

1.  IKK-1 and IKK-2: cytokine-activated IkappaB kinases essential for NF-kappaB activation.

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Journal:  Science       Date:  1997-10-31       Impact factor: 47.728

2.  Induction of apoptotic program in cell-free extracts: requirement for dATP and cytochrome c.

Authors:  X Liu; C N Kim; J Yang; R Jemmerson; X Wang
Journal:  Cell       Date:  1996-07-12       Impact factor: 41.582

Review 3.  A novel strategy for gene therapy and gene regulation analysis using transcription factor decoy oligonucleotides.

Authors:  N Tomita; R Morishita; J Higaki; T Ogihara
Journal:  Exp Nephrol       Date:  1997 Sep-Oct

Review 4.  BCL-2 family: regulators of cell death.

Authors:  D T Chao; S J Korsmeyer
Journal:  Annu Rev Immunol       Date:  1998       Impact factor: 28.527

5.  Apoptosis in the absence of poly-(ADP-ribose) polymerase.

Authors:  M Leist; B Single; G Künstle; C Volbracht; H Hentze; P Nicotera
Journal:  Biochem Biophys Res Commun       Date:  1997-04-17       Impact factor: 3.575

6.  Methylprednisolone inhibition of TNF-alpha expression and NF-kB activation after spinal cord injury in rats.

Authors:  J Xu; G Fan; S Chen; Y Wu; X M Xu; C Y Hsu
Journal:  Brain Res Mol Brain Res       Date:  1998-08-31

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Journal:  Cell       Date:  1993-08-27       Impact factor: 41.582

8.  Bad, a heterodimeric partner for Bcl-XL and Bcl-2, displaces Bax and promotes cell death.

Authors:  E Yang; J Zha; J Jockel; L H Boise; C B Thompson; S J Korsmeyer
Journal:  Cell       Date:  1995-01-27       Impact factor: 41.582

9.  The C. elegans cell death gene ced-3 encodes a protein similar to mammalian interleukin-1 beta-converting enzyme.

Authors:  J Yuan; S Shaham; S Ledoux; H M Ellis; H R Horvitz
Journal:  Cell       Date:  1993-11-19       Impact factor: 41.582

10.  Lamin proteolysis facilitates nuclear events during apoptosis.

Authors:  L Rao; D Perez; E White
Journal:  J Cell Biol       Date:  1996-12       Impact factor: 10.539

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  1 in total

1.  Alteration of NF-kappaB activity leads to mitochondrial apoptosis after infection with pathological prion protein.

Authors:  Soizic Bourteele; Katja Oesterle; Andreas O Weinzierl; Stephan Paxian; Marc Riemann; Roland M Schmid; Oliver Planz
Journal:  Cell Microbiol       Date:  2007-06-15       Impact factor: 3.715

  1 in total

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