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亨氏袢髓质内层细段的三维功能重建

Three-dimensional functional reconstruction of inner medullary thin limbs of Henle's loop.

作者信息

Pannabecker Thomas L, Abbott Diane E, Dantzler William H

机构信息

Department of Physiology, College of Medicine, University of Arizona, Tucson, AZ 85724-5051, USA.

出版信息

Am J Physiol Renal Physiol. 2004 Jan;286(1):F38-45. doi: 10.1152/ajprenal.00285.2003. Epub 2003 Sep 30.

DOI:10.1152/ajprenal.00285.2003
PMID:14519595
Abstract

Digital three-dimensional (3-D) functional reconstructions of inner medullary nephrons were performed. Antibodies against aquaporins (AQP)-1 and -2 and the chloride channel ClC-K1 identified descending thin limbs (DTLs), collecting ducts (CDs), and ascending thin limbs (ATLs), respectively, through indirect immunofluorescence. Tubules were labeled in transverse sections and assembled into 3-D arrays, permitting individual tubule or combined surface representations to depths of 3.3 mm to be viewed in an interactive digital model. Surface representations of 75 tubules positioned near the central region of the inner medulla were reconstructed. In most DTL segments that form loops below 1 mm from the inner medullary base, AQP1 expression begins at the base, becomes intermittent for variable lengths, and continues nearly midway to the loop. The terminal DTL segment exhibiting undetectable AQP1 represents nearly 60% of the distance from the medullary base to the tip of the loop. AQP1 expression was entirely undetectable in shorter long-looped DTLs. ClC-K1 is expressed continuously along the terminal portion of all DTLs reconstructed here, beginning with a prebend region approximately 164 microm before the bend in all tubules and continuing through the entire ascent of the ATLs to the base of the inner medulla. CDs express AQP2 continuously and extensive branching patterns are illustrated. 3-D functional reconstruction of inner medullary nephrons is capable of showing axial distribution of membrane proteins in tubules of the inner medulla and can contribute to further development and refinement of models that attempt to elucidate the concentrating mechanism.

摘要

对内髓肾单位进行了数字三维(3-D)功能重建。通过间接免疫荧光,抗水通道蛋白(AQP)-1和-2以及氯离子通道ClC-K1的抗体分别识别出降支细段(DTL)、集合管(CD)和升支细段(ATL)。肾小管在横切面上被标记,并组装成三维阵列,从而可以在交互式数字模型中查看单个肾小管或组合表面,深度可达3.3毫米。重建了位于内髓中央区域附近的75个肾小管的表面。在大多数距内髓底部1毫米以下形成袢的DTL段中,AQP1表达始于基部,在不同长度上呈间歇性,并几乎持续到袢的中途。未检测到AQP1的终末DTL段占从髓质基部到袢尖端距离的近60%。在较短的长袢DTL中完全检测不到AQP1表达。ClC-K1在此处重建的所有DTL的终末部分沿其连续表达,从所有肾小管弯曲前约164微米的预弯曲区域开始,并持续通过ATL的整个上升过程直至内髓基部。CD持续表达AQP2,并展示了广泛的分支模式。内髓肾单位的三维功能重建能够显示内髓肾小管中膜蛋白的轴向分布,并有助于进一步发展和完善试图阐明浓缩机制的模型。

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