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对人外周血和淋巴组织中Bcl-2家族蛋白(Bcl-2、Bax、Bcl-X和Mcl-1)的细胞表达进行免疫印迹分析。

Immunoblot analysis of cellular expression of Bcl-2 family proteins, Bcl-2, Bax, Bcl-X and Mcl-1, in human peripheral blood and lymphoid tissues.

作者信息

Ohta K, Iwai K, Kasahara Y, Taniguchi N, Krajewski S, Reed J C, Miyawaki T

机构信息

Department of Pediatrics, School of Medicine, Kanazawa University, Ishikawa, Japan.

出版信息

Int Immunol. 1995 Nov;7(11):1817-25. doi: 10.1093/intimm/7.11.1817.

Abstract

The ability of Bcl-2 to inhibit apoptotic cell death is well established. Several homologues of the bcl-2 gene, such as bax, bcl-x or mcl-1, have recently been identified. Like Bcl-2, both Bcl-XL and Mcl-1 appear to function as repressors of apoptotic cell death, whereas Bax facilitates it, indicating possible interactions among them in the control of cellular survival. To investigate the in vivo role of expression of bcl-2 gene family products, immunoblot analysis using corresponding specific antisera was performed for peripheral blood cells and some lymphoid tissues in humans. We demonstrated that all Bcl-2 family proteins were expressed at various levels in hematolymphoid cell subpopulations isolated from peripheral blood, tonsil, spleen and thymus. Lymphoid expression of Bcl-2 family proteins tended to increase following activation, but declined with time in culture. Loss of Bcl-2 in cultured lymphoid cells was especially marked. Sole expression of Bax, but not other members of the Bcl-2 family, was observed on neutrophils, seemingly reflecting their shortest life-span among blood leukocytes. The results support the notion that a balance of expression of Bcl-2 family proteins may regulate the life and death of hematolymphoid cells at different stages of cell differentiation and activation.

摘要

Bcl-2抑制凋亡性细胞死亡的能力已得到充分证实。最近已鉴定出bcl-2基因的几种同源物,如bax、bcl-x或mcl-1。与Bcl-2一样,Bcl-XL和Mcl-1似乎都作为凋亡性细胞死亡的抑制因子发挥作用,而Bax则促进细胞死亡,这表明它们在控制细胞存活方面可能存在相互作用。为了研究bcl-2基因家族产物表达在体内的作用,我们使用相应的特异性抗血清对人类外周血细胞和一些淋巴组织进行了免疫印迹分析。我们证明,所有Bcl-2家族蛋白在从外周血、扁桃体、脾脏和胸腺分离的血液淋巴细胞亚群中均有不同程度的表达。Bcl-2家族蛋白的淋巴细胞表达在激活后趋于增加,但在培养过程中随时间下降。培养的淋巴细胞中Bcl-2的丧失尤为明显。在中性粒细胞上仅观察到Bax的表达,而未观察到Bcl-2家族的其他成员,这似乎反映了它们在血液白细胞中最短的寿命。这些结果支持这样一种观点,即Bcl-2家族蛋白表达的平衡可能在细胞分化和激活的不同阶段调节血液淋巴细胞的生死。

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