Mapara M Y, Bommert K, Bargou R C, Leng C, Beck C, Ludwig W D, Gierschik P, Dörken B
Free University of Berlin, University Medical Center Rudolf Virchow, Robert Rössle Klinik, Department of Internal Medicine, Germany.
Blood. 1995 Apr 1;85(7):1836-42.
Recently G alpha 16, a new guanosine triphosphate (GTP) binding protein alpha subunit has been described to be specifically expressed in human hematopoietic cells. Expression of G alpha 16 was observed in human cell lines of myelomonocytic and T-lymphocytic origin, but not in human B-cell lines Raji and IM9. We studied the expression of G alpha 16 in human B cells corresponding to different stages of B-cell differentiation by means of reverse transcriptase-polymerase chain reaction (RT-PCR) and Western blotting. The human Burkitt's lymphoma cell lines Raji, Ramos, BJAB, the lymphoblastoid cell line SKW6.4, and the plasmocytoma cell line U266 were devoid of G alpha 16. In contrast, G alpha 16 was detected in the human progenitor B cell lines Reh and Nalm-6. Using the mu+, k- cell line BLIN-1 (pre-B cell phenotype) and its derived subclone 1E8 (surface mu+, k+; B-cell phenotype) G alpha 16 expression was found to disappear on transition from pre-B to B-cell differentiation stage. The analysis of a broad panel of human neoplastic B lymphocytes ranging from progenitor B-acute lymphatic leukemia (pre-pre-B-ALL), common acute leukemias (cALL), pre-B-ALL, mature B-ALL to low grade B-cell lymphoma (chronic lymphocytic leukemia of B-cell type, leukemic centrocytic non-Hodgkins lymphoma [NHL], hairy cell leukemia) showed that G alpha 16 expression is limited to progenitor and pre-B-ALL cells. Therefore, we conclude that within B-cell differentiation, G alpha 16 is expressed solely during early B cell ontogeny and downregulated during differentiation. Thus, G alpha 16 might be an important regulator involved in signaling processes in progenitor B cells.
最近,一种新的鸟苷三磷酸(GTP)结合蛋白α亚基——Gα16已被描述为在人类造血细胞中特异性表达。在源自髓单核细胞和T淋巴细胞的人类细胞系中观察到了Gα16的表达,但在人类B细胞系Raji和IM9中未观察到。我们通过逆转录聚合酶链反应(RT-PCR)和蛋白质免疫印迹法研究了Gα16在对应于B细胞分化不同阶段的人类B细胞中的表达。人类伯基特淋巴瘤细胞系Raji、Ramos、BJAB、淋巴母细胞系SKW6.4和浆细胞瘤细胞系U266均缺乏Gα16。相比之下,在人类祖B细胞系Reh和Nalm-6中检测到了Gα16。使用μ⁺、κ⁻细胞系BLIN-1(前B细胞表型)及其衍生的亚克隆1E8(表面μ⁺、κ⁺;B细胞表型),发现Gα16表达在从前B细胞向B细胞分化阶段转变时消失。对一系列广泛的人类肿瘤性B淋巴细胞进行分析,范围从祖B急性淋巴细胞白血病(前前B-ALL)、普通急性白血病(cALL)、前B-ALL、成熟B-ALL到低级别B细胞淋巴瘤(B细胞型慢性淋巴细胞白血病、白血病性中心细胞性非霍奇金淋巴瘤[NHL]、毛细胞白血病),结果表明Gα16表达仅限于祖细胞和前B-ALL细胞。因此,我们得出结论,在B细胞分化过程中,Gα16仅在早期B细胞个体发育期间表达,并在分化过程中下调。因此,Gα16可能是参与祖B细胞信号传导过程的重要调节因子。