CCAAT ENHANCER-BINDING PROTEIN ALPHA C/EBP-ALPHA INHIBITS CELL-PROLIFERATION THROUGH THE P21 (WAF-1/CIP-1/SDI-1) PROTEIN/

C/EBP alpha has a role in growth arrest and differentiation of mouse p readipocytes. To study the mechanism of C/EBP alpha-induced growth arr est, we developed a cell line, HT1, that contained the human C/EBP alp ha gene under Lac repressor control. IPTG-induced C/EBP alpha caused i nhibition of cell proliferation and DNA synthesis as measured by colon y growth assays, cell counting, and BrdU uptake. A number of proteins that are known to be involved in the regulation of the cell cycle, suc h as cyclin-dependent kinase (CDK) 2 and CDK4, proliferating cell nucl ear antigen (PCNA), p53, c-fos, and the CDK inhibitor p16 and p27 were investigated by Western analysis, No change in their expression was o bserved. However, the p21 (WAF-1/CIP-1/SDI-1) protein was significantl y elevated in growth-arrested HT1 cells. Elevation of p21/SDI-1 mRNA ( threefold) and activation of the p21/SDI-1 promoter by C/EBP alpha did not account for the 12- to 20-fold increase in P21/SDI-1 protein. Pro tein synthesis inhibition by cycloheximide (CHX) treatment indicated t hat the half-life of p21/SDI-1 in dividing HT1 cells was similar to 30 min. However, in C/EBP alpha growth-arrested cells, the level of the p21/SDI-1 did not change for >80 min after CHX addition. Our studies d emonstrate that C/EBP alpha activates p21/SDI-1 by increasing p21/SDI- 1 gene expression and by post-translational stabilization of p21/SDI-1 protein. Furthermore, induction of p21/SDI-1 is responsible for the a bility of C/EBP alpha to inhibit proliferation because transcription o f antisense p21/SDI-1 mRNA eliminated growth inhibition by C/EBP alpha .