Literature DB >> 1279330

Differential gene expression between young and senescent, quiescent WI-38 cells.

D L Doggett1, M O Rotenberg, R J Pignolo, P D Phillips, V J Cristofalo.   

Abstract

To investigate age-related changes in gene expression in WI-38 cells, we isolated RNA from young and senescent, quiescent cultures and made subtracted cDNA libraries. Density-arrested cells were incubated in serum-free MCDB-104 for 3 days. RNA was then isolated and subtracted cDNA libraries were made in the phagemid vector pCDM8. Both by picking clones at random from these subtracted libraries and by differential hybridization screening with subtracted cDNA probes from young and senescent cells, we have identified a total of 11 genes for which RNA is expressed differentially in these quiescent young and senescent WI-38 cultures. Two genes, EPC-1 and EPC-A2, with elevated RNA levels in young cells, have sequences which have not previously been identified. Two of the genes with elevated RNA expression in the senescent cells are the mitochondria-coded genes for NADH dehydrogenase subunit 4 and for cytochrome b. We also identified seven other genes with elevated RNA levels in senescent cells. Three of these, LPC-1, LPC-14 and LPC-24, have been partially sequenced and have not previously been identified. These studies show that density-arrested, serum-deprived, quiescent young and senescent cells express a number of genes differentially. These differences are not growth-dependent, but are age-dependent. Our studies also show that the methods employed here, which include careful regulation of the cell cultures and subtraction of the libraries, result in libraries from which differentially expressed genes can be identified, either by random selection or by differential hybridization screening with subtracted probes.

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Year:  1992        PMID: 1279330     DOI: 10.1016/0047-6374(92)90039-g

Source DB:  PubMed          Journal:  Mech Ageing Dev        ISSN: 0047-6374            Impact factor:   5.432


  7 in total

1.  Cataloging altered gene expression in young and senescent cells using enhanced differential display.

Authors:  M H Linskens; J Feng; W H Andrews; B E Enlow; S M Saati; L A Tonkin; W D Funk; B Villeponteau
Journal:  Nucleic Acids Res       Date:  1995-08-25       Impact factor: 16.971

2.  Recombinant pigment epithelium-derived factor PEDF binds vascular endothelial growth factor receptors 1 and 2.

Authors:  Erin K Johnston; Mary K Francis; Janice E Knepper
Journal:  In Vitro Cell Dev Biol Anim       Date:  2015-05-07       Impact factor: 2.416

3.  Pigment epithelium-derived factor (PEDF) shares binding sites in collagen with heparin/heparan sulfate proteoglycans.

Authors:  Atsushi Sekiya; Hitomi Okano-Kosugi; Chisato M Yamazaki; Takaki Koide
Journal:  J Biol Chem       Date:  2011-06-07       Impact factor: 5.157

Review 4.  The effects of PEDF on cancer biology: mechanisms of action and therapeutic potential.

Authors:  S Patricia Becerra; Vicente Notario
Journal:  Nat Rev Cancer       Date:  2013-03-14       Impact factor: 60.716

5.  Donor age-dependent acceleration of cellular aging by repeated ultraviolet A irradiation of human dermal fibroblasts derived from a single donor.

Authors:  Eiji Naru; Toshiro Ohta; Ken Inomata; Akinobu Hayashi; Kazuhiko Kaji
Journal:  Hum Cell       Date:  2009-05       Impact factor: 4.174

6.  Modulation of mitochondrial gene expression in pulmonary epithelial cells exposed to oxidants.

Authors:  Y M Janssen; K E Driscoll; C R Timblin; D Hassenbein; B T Mossman
Journal:  Environ Health Perspect       Date:  1998-10       Impact factor: 9.031

Review 7.  From old organisms to new molecules: integrative biology and therapeutic targets in accelerated human ageing.

Authors:  L S Cox; R G A Faragher
Journal:  Cell Mol Life Sci       Date:  2007-10       Impact factor: 9.261

  7 in total

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