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小鼠发育过程中的Bcl-2蛋白表达。

Bcl-2 protein expression during murine development.

作者信息

Novack D V, Korsmeyer S J

机构信息

Department of Medicine, Howard Hughes Medical Institute, Washington University School of Medicine, St. Louis, Missouri 63110.

出版信息

Am J Pathol. 1994 Jul;145(1):61-73.

PMID:8030757
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1887292/
Abstract

Bcl-2 functions as a death repressor molecule in an evolutionarily conserved cell death pathway. To further explore the role of Bcl-2 in development, we assessed its pattern of expression during murine embryogenesis. Immunohistochemical analysis demonstrates that Bcl-2 is widely expressed early in mouse fetal development in tissues derived from all three germ layers and that this expression becomes restricted with maturation. Within epithelium, the E12.5 lung bud demonstrates a proximal to distal gradient of Bcl-2 expression which is enhanced by E18.5. Bcl-2 is expressed throughout the intestinal epithelium through E14.5, but by E18.5 only cells in the crypts and lower villi express Bcl-2. In the mesoderm-derived kidney, Bcl-2 is expressed in both the ureteric bud and metanephric cap tissue at E12.5. Tubular structures also express Bcl-2, although overall levels drop as the kidney matures. Retinal neuroepithelial cells uniformly express Bcl-2 until cells begin to differentiate and then display the topographic distribution maintained into adulthood. The developing limb provides a clear example where Bcl-2 is restricted to zones of cell survival; Bcl-2 is expressed in the digital zones but not in the interdigital zones of cell death. The wide distribution of Bcl-2 in the developing mouse suggests that many immature cells require a death repressor molecule or that Bcl-2 may have roles beyond regulating developmental cell death.

摘要

Bcl-2在一条进化上保守的细胞死亡途径中作为一种死亡抑制分子发挥作用。为了进一步探究Bcl-2在发育过程中的作用,我们评估了其在小鼠胚胎发生过程中的表达模式。免疫组织化学分析表明,Bcl-2在小鼠胚胎发育早期在源自所有三个胚层的组织中广泛表达,并且这种表达随着成熟而受到限制。在上皮组织中,E12.5期的肺芽显示出Bcl-2表达从近端到远端的梯度,在E18.5期增强。Bcl-2在整个肠上皮中持续表达至E14.5期,但到E18.5期时,只有隐窝和较低绒毛中的细胞表达Bcl-2。在中胚层来源的肾脏中,E12.5期时输尿管芽和后肾帽组织中均表达Bcl-2。肾小管结构也表达Bcl-2,尽管随着肾脏成熟总体水平下降。视网膜神经上皮细胞在细胞开始分化之前均一表达Bcl-2,然后呈现出维持至成年期的拓扑分布。发育中的肢体提供了一个明确的例子,其中Bcl-2局限于细胞存活区域;Bcl-2在指区表达,但在细胞死亡的指间区不表达。Bcl-2在发育中的小鼠体内广泛分布,这表明许多未成熟细胞需要一种死亡抑制分子,或者Bcl-2可能具有除调节发育性细胞死亡之外的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee71/1887292/58ea74ed0b0b/amjpathol00055-0077-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee71/1887292/b1bdbbe38937/amjpathol00055-0069-a.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee71/1887292/3833963a9eee/amjpathol00055-0076-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee71/1887292/58ea74ed0b0b/amjpathol00055-0077-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee71/1887292/b1bdbbe38937/amjpathol00055-0069-a.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee71/1887292/16b843e8b1b6/amjpathol00055-0071-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee71/1887292/57f6158deaf6/amjpathol00055-0072-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee71/1887292/ab03a7104442/amjpathol00055-0073-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee71/1887292/a28eb9dfdcf9/amjpathol00055-0074-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee71/1887292/93fdd69e4956/amjpathol00055-0074-b.jpg
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本文引用的文献

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Bcl-2-deficient mice demonstrate fulminant lymphoid apoptosis, polycystic kidneys, and hypopigmented hair.Bcl-2基因缺陷型小鼠表现出暴发性淋巴细胞凋亡、多囊肾和毛发色素减退。
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Apoptosis: final common pathway of photoreceptor death in rd, rds, and rhodopsin mutant mice.凋亡:rd、rds和视紫红质突变小鼠中光感受器死亡的最终共同途径。
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Bcl-2 blocks apoptosis in cells lacking mitochondrial DNA.Bcl-2可阻止线粒体DNA缺失细胞中的细胞凋亡。
周细胞和星形胶质细胞中的 Bcl-2 表达影响血管发育和稳态。
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BBC3 (PUMA) regulates developmental apoptosis but not axonal injury induced death in the retina.BBC3(PUMA)调节视网膜发育性细胞凋亡,但不调节轴突损伤诱导的细胞死亡。
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BCL-2 is a downstream target of ATF5 that mediates the prosurvival function of ATF5 in a cell type-dependent manner.BCL-2 是 ATF5 的下游靶点,以细胞类型依赖的方式介导 ATF5 的生存促进功能。
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