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甲状旁腺激素对胞质钙的调节以及正常和假性甲状旁腺功能减退患者成纤维细胞中胞质钙的振荡

Regulation of cytosolic calcium by parathyroid hormone and oscillations of cytosolic calcium in fibroblasts from normal and pseudohypoparathyroid patients.

作者信息

Gupta A, Martin K J, Miyauchi A, Hruska K A

机构信息

Renal Divisions, Jewish Hospital of St. Louis, Washington University School of Medicine, Missouri 63110.

出版信息

Endocrinology. 1991 Jun;128(6):2825-36. doi: 10.1210/endo-128-6-2825.

DOI:10.1210/endo-128-6-2825
PMID:1645251
Abstract

UNLABELLED

The second messengers for PTH action on fibroblasts have not been determined. The hypothesis that Ca2+ is a second messenger was examined by spectrofluorometric measurement of cytosolic calcium ([Ca2+]i), of fura-2-loaded human dermal skin fibroblasts. PTH induced: 1) transient elevations of [Ca2+]i due to both Ca2+ influx and intracellular release which were independent of CAMP generation, and 2) membrane depolarization. PTH treatment of fibroblasts depolarized by KCl induced oscillations of [Ca2+]i, but spontaneous oscillatory activity was not observed. Transient elevations of [Ca2+]i similar to that induced by PTH were observed with PTH-related peptide (PTHrp). PTH regulation of [Ca2+]i was normal in fibroblasts from patients with pseudohypoparathyroidism (PHP) type Ia (deficiency of the stimulatory GTP-binding protein, Gs), but PTH induced transient decreases in [Ca2+]i in fibroblasts from patients with PHP type Ib (defective PTH receptor). Both PHP Ia and Ib fibroblasts exhibited: 1) spontaneous [Ca2+]i oscillations, possibly due to voltage gated Ca2+ entry and Ca2+ induced Ca2+ release; and 2) greater sensitivity than normal fibroblasts for release of Ca2+ from intracellular stores when [Ca2+]i was decreased by lowering external Ca2+.

CONCLUSIONS

  1. PTH-induced transient elevations in [Ca2+]i in normal fibroblasts result from Ca2+ entry and intracellular release which are independent of CAMP generation; 2) [Ca2+]i homeostasis is altered in PHP fibroblasts, resulting in Ca2+ oscillations; 3) PTH regulation of [Ca2+]i is altered in PHP Ib, but not in PHP Ia fibroblasts.
摘要

未标记

甲状旁腺激素(PTH)作用于成纤维细胞的第二信使尚未确定。通过用荧光分光光度法测量用fura-2负载的人真皮皮肤成纤维细胞的胞质钙([Ca2+]i),来检验Ca2+是第二信使这一假说。PTH诱导:1)由于Ca2+内流和细胞内释放导致的[Ca2+]i短暂升高,这与环磷酸腺苷(CAMP)生成无关;2)膜去极化。用KCl使成纤维细胞去极化后,PTH处理可诱导[Ca2+]i振荡,但未观察到自发振荡活性。甲状旁腺激素相关肽(PTHrp)可引起类似于PTH诱导的[Ca2+]i短暂升高。I型假性甲状旁腺功能减退症(PHP)(刺激性GTP结合蛋白Gs缺乏)患者的成纤维细胞中,PTH对[Ca2+]i的调节正常,但Ib型PHP患者(PTH受体缺陷)的成纤维细胞中,PTH可诱导[Ca2+]i短暂降低。PHP Ia和Ib成纤维细胞均表现出:1)自发的[Ca2+]i振荡,可能是由于电压门控Ca2+内流和Ca2+诱导的Ca2+释放;2)当通过降低细胞外Ca2+使[Ca2+]i降低时,比正常成纤维细胞对细胞内储存的Ca2+释放更敏感。

结论

1)正常成纤维细胞中PTH诱导的[Ca2+]i短暂升高是由Ca2+内流和细胞内释放引起的,与CAMP生成无关;2)PHP成纤维细胞中[Ca2+]i稳态改变,导致Ca2+振荡;3)PTH对[Ca2+]i的调节在PHP Ib成纤维细胞中改变,但在PHP Ia成纤维细胞中未改变。

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