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Discovery of α-Klotho unveiled new insights into calcium and phosphate homeostasis

α-Klotho was first identified as the responsible gene in a mutant mouse line whose disruption results in a variety of premature aging-related phenotypes. α-Klotho has been shown to participate in the regulation of parathyroid hormone secretion and trans-epithelial transport of Ca(2+) in the choroid...

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Detalles Bibliográficos
Autor principal: Nabeshima, Yo-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Academy 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3524302/
https://www.ncbi.nlm.nih.gov/pubmed/19282648
http://dx.doi.org/10.2183/pjab/85.125
Descripción
Sumario:α-Klotho was first identified as the responsible gene in a mutant mouse line whose disruption results in a variety of premature aging-related phenotypes. α-Klotho has been shown to participate in the regulation of parathyroid hormone secretion and trans-epithelial transport of Ca(2+) in the choroid plexus and kidney. α-Klotho, acting as a cofactor for FGF23, is also a major regulator of vitamin D biosynthesis and phosphate reabsorption in the kidney. These suggest that α-Klotho is a key player that integrates a multi-step regulatory system of calcium and phosphate homeostasis. Collectively, the molecular function of α-Klotho reveals a new paradigm that may change current concepts in mineral homeostasis and give rise to new insights in this field.