Drach J, Zhao S, Malavasi F, Mehta K
Department of Hematology, University of Texas M.D. Anderson Cancer Center, Houston 77030.
Biochem Biophys Res Commun. 1993 Sep 15;195(2):545-50. doi: 10.1006/bbrc.1993.2080.
The CD38 or T10 molecule is one of the least understood differentiation antigens. Virtually no information is available on the regulation and functions of CD38 antigen in hematopoietic cells. Using human promyelocytic leukemia cells, we demonstrate that all trans-retinoic acid is a potent and specific inducer of CD38 expression in myeloid lineage. At physiological doses, all trans-retinoic acid induces significant levels (8 to 10-fold) of CD38. Similarly, in patients with promyelocytic leukemia, a significant increase (3 to 6-fold) in CD38 expression was observed in vivo following single oral dose administration of all trans-retinoic acid. The induction of CD38 is a specific response of myeloid cells to retinoic acid and is not seen with other agents that induce differentiation. We believe that the induction of CD38 antigen is an early event in retinoid-regulated gene expression in normal and transformed myeloid cells.
CD38或T10分子是人们了解最少的分化抗原之一。关于造血细胞中CD38抗原的调节和功能,几乎没有可用信息。利用人早幼粒细胞白血病细胞,我们证明全反式维甲酸是髓系谱系中CD38表达的一种强效且特异性诱导剂。在生理剂量下,全反式维甲酸可诱导显著水平(8至10倍)的CD38表达。同样,在早幼粒细胞白血病患者中,单次口服全反式维甲酸后,体内观察到CD38表达显著增加(3至6倍)。CD38的诱导是髓系细胞对维甲酸的特异性反应,而其他诱导分化的药物则不会出现这种情况。我们认为,CD38抗原的诱导是正常和转化髓系细胞中类维生素A调节基因表达的早期事件。