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lüll Toward a comprehensive molecular model of active calcium reabsorption Hoenderop JG; Willems PH; Bindels RJAm J Physiol Renal Physiol 2000[Mar]; 278 (3): F352-60The fine tuning of Ca(2+) excretion in the kidney takes place in the distal nephron, which consists of the distal convoluted tubule, connecting tubule, and initial portion of the cortical collecting duct. In these segments, Ca(2+) is reabsorbed through an active transcellular pathway. The apical influx of Ca(2+) into the distal renal cell is presumably the rate-limiting step in this process, and its molecular identity has remained obscure so far. The recently discovered epithelial Ca(2+) channel (ECaC) exhibits the expected properties for being the gatekeeper in transcellular Ca(2+) reabsorption. The characteristics and potential physiological role of ECaC will be discussed in this review. Our knowledge of the mechanisms involved in the regulation of transcellular Ca(2+) transport has advanced rapidly since the development of cell models originating from distal tubular cells. Studies using these models indicate that hormones including arginine vasopressin, PGE(2), adenosine, ATP, and atrial natriuretic peptide should be considered as calciotropic hormones controlling renal Ca(2+) handling. Evidence is now beginning to emerge that the stimulating calciotropic hormones utilize new cAMP-independent pathways to stimulate Ca(2+) reabsorption. These new findings allow the development of a comprehensive and detailed model of the process of transcellular calcium transport in the kidney whereby the individual contribution of the participating transporters can now be fully appreciated.|*Models, Molecular[MESH]|Absorption[MESH]|Amino Acid Sequence/genetics[MESH]|Animals[MESH]|Calcium/*metabolism[MESH]|Carrier Proteins/metabolism[MESH]|Epithelial Sodium Channels[MESH]|Hormones/physiology[MESH]|Humans[MESH]|Molecular Sequence Data[MESH]|Sodium Channels/genetics[MESH] |