首页> 外文期刊>Developmental dynamics: an official publication of the American Association of Anatomists >Macrophage and microglia ontogeny in the mouse visual system can be traced by the expression of Cathepsins B and D.
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Macrophage and microglia ontogeny in the mouse visual system can be traced by the expression of Cathepsins B and D.

机译:小鼠视觉系统中的巨噬细胞和小胶质细胞瘤发生可以通过组织蛋白酶B和D的表达来追踪。

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摘要

Here, we show a detailed chronotopographical analysis of cathepsin B and D expression during development of the mouse visual system. Both proteases were detected in large rounded/ameboid cells usually located in close relationship with prominent sites of extensive physiological cell death. In concordance with their morphological features and topographical distribution, we demonstrate that expressing cells corresponded with macrophages and microglial precursors. We found that as microglial precursors differentiated the expression of both cathepsins was down-regulated. Of interest, cathepsin B and D transcripts were never observed in degenerating cells. Our findings point to a role for cathepsin D and B in cell debris degradation after apoptotic processes rather than promoting cell death, as proposed for other developmental models. Additionally their pattern of expression suggests a role in the maturation of the microglial precursors.
机译:在这里,我们显示了组织视觉B和D表达的小鼠视觉系统发育过程中的详细时序地形分析。两种蛋白酶都在大的圆形/类动物细胞中检测到,通常与广泛的生理性细胞死亡的显着位点紧密相关。根据它们的形态特征和地形分布,我们证明了表达细胞与巨噬细胞和小胶质前体相对应。我们发现,随着小胶质细胞前体的分化,两种组织蛋白酶的表达均被下调。有趣的是,从未在退化细胞中观察到组织蛋白酶B和D转录本。我们的发现指向组织蛋白酶D和B在凋亡过程后细胞碎片降解中的作用,而不是促进细胞死亡,这是针对其他发育模型提出的。另外,它们的表达模式表明在小胶质前体的成熟中起作用。

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