PROTEIN-KINASE-C ISOFORMS IN MURINE ERYTHROLEUKEMIA-CELLS AND THEIR INVOLVEMENT IN THE DIFFERENTIATION PROCESS

Citation
M. Patrone et al., PROTEIN-KINASE-C ISOFORMS IN MURINE ERYTHROLEUKEMIA-CELLS AND THEIR INVOLVEMENT IN THE DIFFERENTIATION PROCESS, FEBS letters, 344(1), 1994, pp. 91-95
Citations number
16
Categorie Soggetti
Biophysics,Biology
Journal title
ISSN journal
00145793
Volume
344
Issue
1
Year of publication
1994
Pages
91 - 95
Database
ISI
SICI code
0014-5793(1994)344:1<91:PIIMEA>2.0.ZU;2-H
Abstract
In addition to alpha, delta and epsilon-protein kinase C, murine eryth roleukemia cells contain xi-PKC and also a c-PKC isoform, named alpha( 1), which shows cross-reactivity with an anti-alpha-PKC antipeptide an tibody. In a C44 MEL cell clone, characterized by a high rate of diffe rentiation, both c-PKC forms are expressed al a level higher than that of the N23 MEL cell clone which differentiates at a low rate and cont ains higher levels of epsilon-PKC and particularly of the delta-PKC is ozyme. In the course of MEL cell differentiation, delta-PKC in N23 cel ls and alpha(1)-PKC in C44 cells are rapidly down-regulated and the ov erall process is almost completed before cell commitment. Of the other three PKC isozymes present in both clones, only alpha-PKC is down-reg ulated to a significant extent. It is proposed that modulation of the signal delivered by each PKC isozyme is one of the biochemical mechani sms involved in MEL cell differentiation.