Goldschmidt Imeke, Grahammer Florian, Warth Richard, Schulz-Baldes Annette, Garty Haim, Greger Rainer, Bleich Markus
Physiologisches Institut, Albert-Ludwigs Universität Freiburg, Germany.
Cell Physiol Biochem. 2004;14(1-2):113-20. doi: 10.1159/000076932.
Corticosteroid hormone induced factor (CHIF) is a small epithelial-specific protein regulated by aldosterone and K+ intake. It is a member of the FXYD family of single span transmembrane proteins involved in the regulation of ion transport. Recent data have suggested that CHIF interacts with the a subunit of the Na+-K+-ATPase and increases the pump's affinity to cell Na+. CHIF knockout (KO) mice have mild renal phenotype under low Na+ or high K+ diets. The present study further characterizes kidney electrolyte metabolism in CHIF KO mice and describes abnormalities in the colonic ion transport function. Kidney: KO mice were not compromised in salt and water balance under resting conditions. Fractional excretions (FE) of Na+ and K+ were normal and the animals had no deficit in the adaptation to low Na+ or high K+ intake. Glucocorticoid treatment did not unmask any difference. The effects of amiloride on Na+ absorption were not different at any treatment protocol. In contrast, FEK+ was reduced by 35% in KO mice under low Na+ intake. COLON: Amiloride inhibitable Na+ absorption was reduced in distal colon by 42%, 54% and 58% under control conditions, glucocorticoid treatment and low Na+ intake, respectively. Also, the cAMP dependent ion transport was significantly diminished. Forskolin induced equivalent short circuit current (I'SC) was reduced by 41%, 32% and 58%, under control conditions, high K+, and low Na+ intake, respectively. The present findings support a role of CHIF as an indirect modulator of several different ion transport mechanisms and are consistent with regulation of the Na+-K+-ATPase as the common denominator.
皮质类固醇激素诱导因子(CHIF)是一种受醛固酮和钾摄入调节的小上皮特异性蛋白。它是参与离子转运调节的单跨膜蛋白FXYD家族的成员。最近的数据表明,CHIF与钠钾ATP酶的α亚基相互作用,并增加该泵对细胞内钠的亲和力。CHIF基因敲除(KO)小鼠在低钠或高钾饮食条件下具有轻度肾脏表型。本研究进一步描述了CHIF KO小鼠的肾脏电解质代谢特征,并描述了结肠离子转运功能的异常情况。肾脏:KO小鼠在静息状态下的盐和水平衡未受影响。钠和钾的排泄分数(FE)正常,并且动物在适应低钠或高钾摄入方面没有缺陷。糖皮质激素治疗未揭示任何差异。在任何治疗方案下,氨氯地平对钠吸收的影响均无差异。相比之下,在低钠摄入条件下,KO小鼠的FEK+降低了35%。结肠:在对照条件、糖皮质激素治疗和低钠摄入情况下,氨氯地平可抑制的远端结肠钠吸收分别降低了42%、54%和58%。此外,环磷酸腺苷(cAMP)依赖性离子转运也显著减少。在对照条件、高钾和低钠摄入情况下,福斯可林诱导的等效短路电流(I'SC)分别降低了41%、32%和58%。本研究结果支持CHIF作为几种不同离子转运机制的间接调节因子的作用,并且与将钠钾ATP酶的调节作为共同特征相一致。