Pantazis P, Sariban E, Kufe D, Antoniades H N
Proc Natl Acad Sci U S A. 1986 Sep;83(17):6455-9. doi: 10.1073/pnas.83.17.6455.
Phorbol esters induce the differentiation of human myeloid leukemia cells HL-60 and U-937 along the monocytic-macrophage lineage. This process has been associated with the induction of several cellular protooncogenes, including the c-fos and c-fms genes. We now report that phorbol ester-induced differentiation of the HL-60 and U-937 cells results in the induction of the expression of the c-sis platelet-derived growth factor 2 (PDGF-2) protooncogene. sis mRNA transcripts were not detectable in the uninduced cells but were detectable within 12 hr of phorbol ester induction. Concomitantly, the induced cells were shown to synthesize and secrete biologically active PDGF-like proteins, identified in the conditioned medium of the phorbol ester-treated cells by direct immunoprecipitation with PDGF antiserum. Addition of cycloheximide to phorbol ester-treated HL-60 cells superinduced sis mRNA transcripts. c-sis gene transcripts were also detected in freshly isolated human monocytes but not in human granulocytes or in HL-60 cells induced to differentiate along the granulocytic lineage. Activation of the c-sis/PDGF-2 gene in human hematopoietic cells during monocytic differentiation may serve in the mediation of physiologic functions of the differentiated cells by means of the secretion of potent PDGF-like mitogen.
佛波酯可诱导人髓系白血病细胞HL - 60和U - 937沿单核巨噬细胞谱系分化。这一过程与多种细胞原癌基因的诱导有关,包括c - fos和c - fms基因。我们现在报告,佛波酯诱导HL - 60和U - 937细胞分化会导致c - sis血小板衍生生长因子2(PDGF - 2)原癌基因表达的诱导。在未诱导的细胞中检测不到sis mRNA转录本,但在佛波酯诱导后12小时内可检测到。同时,诱导的细胞被证明能合成并分泌具有生物活性的类PDGF蛋白,通过用PDGF抗血清直接免疫沉淀在佛波酯处理细胞的条件培养基中鉴定出来。向佛波酯处理的HL - 60细胞中添加环己酰亚胺可超诱导sis mRNA转录本。在新鲜分离的人单核细胞中也检测到c - sis基因转录本,但在人粒细胞或沿粒细胞谱系诱导分化的HL - 60细胞中未检测到。在单核细胞分化过程中,人造血细胞中c - sis/PDGF - 2基因被激活,可能通过分泌强效的类PDGF有丝分裂原介导分化细胞的生理功能。