TY - JOUR
T1 - Correlation between levels of δ protein kinase C and resistance to differentiation in murine erythroleukemia cells
AU - Patrone, Mauro
AU - Pessino, Anna
AU - Passalacqua, Mario
AU - Sparatore, Bianca
AU - Melloni, Edon
AU - Pontremoli, Sandro
N1 - Funding Information:
This work was supported, in part, by grants from the Italian Consiglio Nazionale delle Ricerche, Progetto Finalizzato ACRO, from the Associazione Italiana per la Ricerca sul Cancro (AIRC) and from the Ministero dell’Università e della Ricerca Scientifica e Tecnologica (MURST).
PY - 1996/3/7
Y1 - 1996/3/7
N2 - It has been demonstrated that the level of δ protein kinase C is inversely correlated to the responsiveness of murine erythroleukemia cells to chemical induction to terminal erythroid differentiation. In these cells, δPKC is largely present in a membrane associated form, and thus in a constitutively active state, a condition which characterizes the undifferentiated phenotype. Accordingly, commitment to cell differentiation has been shown to be preceded by down regulation of δPKC, a process significantly accelerated and induced to almost completion by the differentiation enhancing factor (DEF) in a dose dependent manner. The present results provide a better understanding of the role of δPKC in characterizing the undifferentiated MEL cell phenotype, and suggest a relationship between the acceleration in the rate of differentiation induced by DEF and the down regulation of this kinase form.
AB - It has been demonstrated that the level of δ protein kinase C is inversely correlated to the responsiveness of murine erythroleukemia cells to chemical induction to terminal erythroid differentiation. In these cells, δPKC is largely present in a membrane associated form, and thus in a constitutively active state, a condition which characterizes the undifferentiated phenotype. Accordingly, commitment to cell differentiation has been shown to be preceded by down regulation of δPKC, a process significantly accelerated and induced to almost completion by the differentiation enhancing factor (DEF) in a dose dependent manner. The present results provide a better understanding of the role of δPKC in characterizing the undifferentiated MEL cell phenotype, and suggest a relationship between the acceleration in the rate of differentiation induced by DEF and the down regulation of this kinase form.
UR - http://www.scopus.com/inward/record.url?scp=0029921563&partnerID=8YFLogxK
U2 - 10.1006/bbrc.1996.0350
DO - 10.1006/bbrc.1996.0350
M3 - Article
SN - 0006-291X
VL - 220
SP - 26
EP - 30
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 1
ER -