| Literature DB >> 25977312 |
Ming Chang Hu1, Mingjun Shi2, Jianning Zhang3, Tayo Addo3, Han Ju Cho2, Sarah L Barker4, Priya Ravikumar5, Nancy Gillings2, Ao Bian2, Sachdev S Sidhu4, Makoto Kuro-o6, Orson W Moe7.
Abstract
αKlotho is a multifunctional protein highly expressed in the kidney. Soluble αKlotho is released through cleavage of the extracellular domain from membrane αKlotho by secretases to function as an endocrine/paracrine substance. The role of the kidney in circulating αKlotho production and handling is incompletely understood, however. Here, we found higher αKlotho concentration in suprarenal compared with infrarenal inferior vena cava in both rats and humans. In rats, serum αKlotho concentration dropped precipitously after bilateral nephrectomy or upon treatment with inhibitors of αKlotho extracellular domain shedding. Furthermore, the serum half-life of exogenous αKlotho in anephric rats was four- to five-fold longer than that in normal rats, and exogenously injected labeled recombinant αKlotho was detected in the kidney and in urine of rats. Both in vivo (micropuncture) and in vitro (proximal tubule cell line) studies showed that αKlotho traffics from the basal to the apical side of the proximal tubule via transcytosis. Thus, we conclude that the kidney has dual roles in αKlotho homeostasis, producing and releasing αKlotho into the circulation and clearing αKlotho from the blood into the urinary lumen.Entities:
Keywords: Cell & Transport Physiology; Nephrectomy; Transcytosis; [REMOVED HYPERLINK FIELD]Klotho; distal tubule; renal proximal tubule cell
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Year: 2015 PMID: 25977312 PMCID: PMC4696570 DOI: 10.1681/ASN.2014101030
Source DB: PubMed Journal: J Am Soc Nephrol ISSN: 1046-6673 Impact factor: 10.121