Changes in the expression of c-myc, RB and tyrosine-phosphorylated proteins during proliferation of NIH 3T3 cells induced by hyaluronic acid.
- Author:
Soon Ok MOON
1
;
Ji Hyun LEE
;
Tai Jin KIM
Author Information
1. Division of Life Science, University of Suwon, Korea.
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
proliferation;
tyrosine phosphorylation;
c-myc;
pRb;
hyaluronic acid
- MeSH:
3T3 Cells;
Amiloride/pharmacology;
Animal;
Cell Division;
Dose-Response Relationship, Drug;
Egtazic Acid/pharmacology;
Hyaluronic Acid/pharmacology*;
Mice;
Mitogens/pharmacology*;
Phosphoproteins/metabolism*;
Phosphorylation;
Proto-Oncogene Proteins c-myc/metabolism*;
Retinoblastoma Protein/metabolism*;
Signal Transduction;
Sodium-Hydrogen Antiporter/antagonists & inhibitors;
Tyrosine
- From:Experimental & Molecular Medicine
1998;30(1):29-33
- CountryRepublic of Korea
- Language:English
-
Abstract:
We have shown that hyaluronic acid stimulates the proliferation of quiescent NIH 3T3 cells. We have shown that treatment of 1 mg/ml hyaluronic acid results in increase of tyrosine phosphorylation of two proteins, MW 124 kDa and 60 kDa as detected by anti-tyrosine antibodies by Western blot analysis. Maximum phosphorylation occurred within 2 h after addition of 1 mg/ml hyaluronic acid. Stimulation of proliferation was also accompanied by increase in c-Myc protein, which was inhibited by amlloride, an inhibitor of Na+/H+ antiporter and EGTA and increase in the steady state level of pRb, the RB gene product. These results suggest that the intracellular signal transduction pathways that mediate the stimulatory effects of hyaluronic acid on cellular proliferation are similar to those of growth factors.
