Endocrinology. 1989 Dec;125(6):3029-36. doi: 10.1210/endo-125-6-3029.

Follicle-stimulating hormone receptor-mediated uptake of 45Ca2+ by proteoliposomes and cultured rat sertoli cells: evidence for involvement of voltage-activated and voltage-independent calcium channels.

Endocrinology

P Grasso, L E Reichert

PMID: 2555135 DOI: 10.1210/endo-125-6-3029

Abstract

We have previously reported incorporation into liposomes of Triton X-100-solubilized FSH receptor-G-protein complexes derived from purified bovine calf testis membranes. In the present study we have used this model system to show that FSH induces flux of 45Ca2+ into such proteoliposomes in a hormone-specific concentration-dependent manner. FSH, inactivated by boiling, had no stimulatory effect on 45Ca2+ flux, nor did isolated alpha- or beta-subunits of FSH. Addition of GTP (or its analogs 5'-guanylylimidodiphosphate and guanosine-5'-O-[3-thiotriphosphate]) or sodium fluoride (in the presence or absence of GTP or its analogs) failed to induce 45Ca2+ flux into proteoliposomes, suggesting that the uptake of 45Ca2+ was receptor, and not G-protein, related. Voltage-independent (ruthenium red and gadolinium chloride) and voltage-activated (methyoxyverapamil and nifedipine) calcium channel-blocking agents reduced FSH-stimulated 45Ca2+ flux into proteoliposomes to control levels. FSH also induced uptake of 45Ca2+ by cultured rat Sertoli cells. Ruthenium red and gadolinium chloride had no effect on basal levels of 45Ca2+ uptake or estradiol secretion by cultured rat Sertoli cells, nor did methoxyverapamil or nifedipine. All four calcium channel blockers, however, were able to reduce FSH-induced 45Ca2+ uptake to basal levels and FSH-stimulated conversion of androstenedione to estradiol by up to 50%, indicating an involvement of Ca2+ in FSH-stimulated steroidogenesis. Our results suggest that the well documented changes in intracellular calcium levels consequent to FSH binding may be due, at least in part, to an influx of calcium through FSH receptor-regulated calcium channels.

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Substances

• Calcium Channel Blockers
• Calcium Channels
• Calcium Radioisotopes
• Liposomes
• Receptors, FSH
• Androstenedione
• Estradiol
• Guanosine Triphosphate
• Follicle Stimulating Hormone
• GTP-Binding Proteins
• Calcium

MeSH terms

• Androstenedione / metabolism
• Animals
• Calcium / metabolism
• Calcium Channel Blockers / pharmacology
• Calcium Channels / physiology
• Calcium Radioisotopes
• Cattle
• Cells, Cultured
• Estradiol / metabolism
• Follicle Stimulating Hormone / pharmacology
• GTP-Binding Proteins / physiology
• Guanosine Triphosphate / pharmacology
• Liposomes / metabolism
• Male
• Receptors, FSH / physiology
• Sertoli Cells / drug effects
• Sertoli Cells / metabolism

Publication Types

• Journal Article
• Research Support, U.S. Gov't, P.H.S.

Grant support

• HD-07252/HD/NICHD NIH HHS/United States
• HD-13938/HD/NICHD NIH HHS/United States

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