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The kidney is a major site of insulin metabolism removing the hormone from the circulation by means of glomerular filtration and by extraction from the postglomerular peritubular circulation. Insulin removed binds to specific receptors in the apical and basolateral tubular membranes. Filtered insulin is internalized by endocytosis and degraded completely. However the role of receptors in mediating endocytosis, the intracellular pathway for insulin, and the contributin of lysosomal and extralysosomal compartments to the degradative process are poorly defined. Basolateral uptake form the peritubular circulation is also followed by degradation but it is not known whether internalization is a prerequisite. Indeed in contrast to the apical side of the cell, basolateral endocytosis is a minor process. The aim of this study are; 1) To evaluate the role of insulin receptors in mediating the renal uptake and degradation of insulin. 2) To characterize the intracellular pathways involved in the apical and basolateral uptake and degradation of insulin. 3) To characterize the products of insulin degradation and thereby to further our understanding of renal epithelial insulin metabolism. Studies will be conducted with kidneys from rats, and with cultured opossum kidney cell line and primary rabbit proximal tubular epithelial cells. Methodology includes subcellular fractionation, electron microscopic autoradiography, cell culture and high pressure liquid chromatography. These studies are particularly significant because of the major role played by the kidney in insulin metabolism. New information will be generated that should achieve our objectives of enhancing the understanding of renal insulin metabolism. In the long term, knowledge gained from this study should contribute significantly to our understanding of the physiology of insulin metabolism in general and in particular will form the basis of elucidating the pathophysiology of alterations of renal insulin metabolism that may occur in disease states.
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Basolateral and apical binding, internalization, and degradation of insulin by cultured kidney epithelial cells.
培养的肾上皮细胞对胰岛素的基底外侧和顶端结合、内化和降解。
DOI: 10.1152/ajpendo.1989.257.6.e895
发表时间: 1989
期刊: The American journal of physiology
影响因子: --
作者: [Rabkin,R, Yagil,C, Frank,B]
通讯作者: Frank,B
Amino acids enhance renal tubular absorption of the los-molecular-weight proteins insulin and growth hormone.
氨基酸增强肾小管对低分子量蛋白质胰岛素和生长激素的吸收。
DOI: 10.1152/ajprenal.1982.242.6.f745
发表时间: 1982
期刊: The American journal of physiology
影响因子: --
作者: [Rabkin,R, Gottheiner,TI, Tsao,TS]
通讯作者: Tsao,TS
Endosomes degrade insulin.
内体降解胰岛素。
DOI: --
发表时间: 1993
期刊: Contributions to nephrology
影响因子: --
作者: [Fawcett,J, Rabkin,R]
通讯作者: Rabkin,R
Renal metabolism of peptide hormones.
肽类激素的肾脏代谢。
DOI: --
发表时间: 1983
期刊: Mineral and electrolyte metabolism
影响因子: --
作者: [Rabkin,R, Kitaji,J]
通讯作者: Kitaji,J
15
    Testosterone Replacement Therapy in Advanced Chronic Kidney Disease
    Muscle Wasting in Uremia
    Muscle Wasting in Uremia
    Muscle Wasting in Uremia
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