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转化生长因子βⅡ型受体在大鼠肾血管发育中的作用:定位于肾小球旁细胞。

TGF-beta type II receptor in rat renal vascular development: localization to juxtaglomerular cells.

作者信息

Liu A, Ballermann B J

机构信息

Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

出版信息

Kidney Int. 1998 Mar;53(3):716-25. doi: 10.1046/j.1523-1755.1998.00810.x.

Abstract

To further define the role of transforming growth factor-beta (TGF-beta) receptors in renal vascular development, detailed immunohistochemical studies of TGF-beta receptor expression were performed from gestational day 15 through adulthood. On gestational day 15, TGF-beta type II receptor immunoreactivity was restricted to perirenal stromal and vascular cells. On gestational day 17 TGF-beta type II receptor immunoreactive stromal cells were observed within the kidney, with the same distribution as stromal alpha-smooth muscle actin and renin immunoreactive cells, and intense stromal TGF-beta type II receptor immunoreactivity continued through postnatal day 5. As vascular development progressed, TGF-beta type II receptor, alpha-smooth muscle actin and renin immunoreactivity became progressively restricted to small renal arteries and arterioles. Expression of TGF-beta type II receptors and renin was very intense in afferent glomerular arterioles during postnatal days 5 to 15, and then became progressively restricted only to juxtaglomerular cells in the mature kidney. TGF-beta type I receptor (ALK-5, ALK-1 and ALK-2) immunoreactivity was not detected in stromal or vascular elements during development or in the mature kidney. Intense TGF-beta type II receptor expression in renal stromal vascular smooth muscle cell precursors and developing blood vessels suggests a role for the TGF-beta type II receptors in the formation of the renal vascular smooth muscle compartment. The continued intense expression in juxtaglomerular cells argues for a role in renin synthesis and/or release. The absence of ALK-5, ALK-1, and ALK-2 in developing vascular smooth muscle and mature juxtaglomerular cells indicates that the canonical view of TGF-beta signaling may not hold in these locations.

摘要

为了进一步明确转化生长因子-β(TGF-β)受体在肾血管发育中的作用,我们进行了从妊娠第15天到成年期的TGF-β受体表达的详细免疫组织化学研究。在妊娠第15天,TGF-β II型受体免疫反应性局限于肾周基质和血管细胞。在妊娠第17天,在肾内观察到TGF-β II型受体免疫反应性基质细胞,其分布与基质α-平滑肌肌动蛋白和肾素免疫反应性细胞相同,并且强烈的基质TGF-β II型受体免疫反应性持续到出生后第5天。随着血管发育的进展,TGF-β II型受体、α-平滑肌肌动蛋白和肾素免疫反应性逐渐局限于小肾动脉和小动脉。在出生后第5至15天,TGF-β II型受体和肾素在入球小动脉中的表达非常强烈,然后在成熟肾脏中逐渐仅局限于球旁细胞。在发育过程中或成熟肾脏的基质或血管成分中未检测到TGF-β I型受体(ALK-5、ALK-1和ALK-2)免疫反应性。肾基质血管平滑肌细胞前体和发育中的血管中强烈的TGF-β II型受体表达表明TGF-β II型受体在肾血管平滑肌隔室形成中起作用。球旁细胞中持续的强烈表达表明其在肾素合成和/或释放中起作用。发育中的血管平滑肌和成熟球旁细胞中不存在ALK-5、ALK-1和ALK-2表明TGF-β信号传导的经典观点在这些部位可能不成立。

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