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Bcl-2家族成员与疾病。

Bcl-2 family members and disease.

作者信息

Sorenson Christine M

机构信息

Department of Pediatrics, University of Wisconsin-Madison, H4/444 CSC, 600 Highland Ave., Madison, WI 53792-4108, USA.

出版信息

Biochim Biophys Acta. 2004 Mar 1;1644(2-3):169-77. doi: 10.1016/j.bbamcr.2003.08.010.

Abstract

Apoptosis plays an important role during development and in the maintenance of multicellular organisms. Bcl-2 family members affect cell death in either a positive or negative fashion. Although some redundancy exists between family members, expression of certain family members is important during development in an organ-specific manner. The founding family member bcl-2 tends to be highly expressed in the embryo and declines postnatally following differentiation and maturation. Altered expression of bcl-2, as well as other family members, has been observed in disease states potentially affecting treatment modalities. Here we examine the distribution and role death repressors bcl-2, bcl-x(L) and bcl-w as well as death effectors bax and bak play regulating apoptosis in a tissue-specific manner. Understanding the normal role of these proteins during embryogenesis and in the mature organ will give us important insight into what goes awry in various disease states.

摘要

细胞凋亡在多细胞生物体的发育和维持过程中发挥着重要作用。Bcl-2家族成员以正向或负向方式影响细胞死亡。尽管家族成员之间存在一些冗余,但某些家族成员的表达在发育过程中以器官特异性方式发挥重要作用。家族创始成员bcl-2在胚胎中往往高度表达,出生后随着分化和成熟而下降。在可能影响治疗方式的疾病状态中,已观察到bcl-2以及其他家族成员的表达改变。在这里,我们研究死亡抑制因子bcl-2、bcl-x(L)和bcl-w以及死亡效应因子bax和bak在以组织特异性方式调节细胞凋亡中所起的分布和作用。了解这些蛋白质在胚胎发生过程中和成熟器官中的正常作用,将使我们深入了解各种疾病状态中出现的问题。

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