The LβT2 clonal gonadotrope

A model for single cell studies of endocrine cell secretion

Paul Thomas, Pamela L. Mellon, Judith L Turgeon, Dennis W. Waring

Research output: Contribution to journalArticle

113 Citations (Scopus)

Abstract

We have used single gonadotropes from the newly derived line, LβT2, to investigate the modulation of Ca2+ signaling and exocytosis by the steroid hormone environment. This cell line, derived by targeted oncogenesis in transgenic mice, has recently been shown to secrete LH in response to GnRH. We have characterized the effects of both GnRH and membrane depolarization on exocytosis and intracellular [Ca2+]([Ca2+](i)) in individual LβT2 cells. GnRH (1-100 nM) evoked concentration-dependent increases in [Ca2+](i) and secretion, as monitored by measurement of plasma membrane capacitance (C(m)) using the whole-cell perforated-patch technique, and the extent of these changes were dependent upon steroid hormone background. GnRH treatment of cells cultured in medium containing charcoal-treated FBS (ct-FBS) showed smaller changes in [Ca2+](i) than cells cultured in untreated FBS. However, when estradiol (E2) and dexamethasone (Dex) were added to the ct-FBS medium (E2/Dex-ct-FBS), the elevations in [Ca2+](i) stimulated by GnRH increased almost 2-fold. Additionally, the rates of secretion in the E2/Dex-ct-FBS- cultured cells were greater than in either ct-FBS- or FBS-cultured cells. The increase in secretory response observed with E2/Dex-ct-FBS appeared to be due to both an increase in the peak [Ca2+](i) stimulated by GnRH and a shift toward increased sensitivity of the Ca2+ dependency of exocytosis. In contrast to GnRH-evoked responses, the increases in [Ca2+](i) elicited by depolarization were greater in cells cultured in ct-FBS than in E2/Dex-ct- FBS; however, the secretory rates were no different in the two groups. Likewise, there was no apparent effect of steroid treatment on the Ca2+ dependency of depolarization-evoked exocytosis. In summary, these results 1) clearly demonstrate the utility of this cell line for single-cell studies of both agonist- and depolarization-evoked secretion; 2) reveal that steroid hormone background has profound effects on LβT2 cells, both on stimulus- induced calcium mobilization and on the apparent Ca2+-sensitivity of exocytosis; and 3) show that expression of the steroid hormone effect on Ca2+-sensitivity is dependent upon receptor occupation by GnRH.

Original languageEnglish (US)
Pages (from-to)2979-2989
Number of pages11
JournalEndocrinology
Volume137
Issue number7
DOIs
StatePublished - 1996

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Endocrine Cells
Charcoal
Gonadotropin-Releasing Hormone
Exocytosis
Dexamethasone
Cultured Cells
Steroids
Hormones
Secretory Rate
LHRH Receptors
Cell Line
Transgenic Mice
Estradiol
Carcinogenesis
Cell Membrane
Calcium
Membranes

ASJC Scopus subject areas

  • Endocrinology
  • Endocrinology, Diabetes and Metabolism

Cite this

The LβT2 clonal gonadotrope : A model for single cell studies of endocrine cell secretion. / Thomas, Paul; Mellon, Pamela L.; Turgeon, Judith L; Waring, Dennis W.

In: Endocrinology, Vol. 137, No. 7, 1996, p. 2979-2989.

Research output: Contribution to journalArticle

Thomas, Paul ; Mellon, Pamela L. ; Turgeon, Judith L ; Waring, Dennis W. / The LβT2 clonal gonadotrope : A model for single cell studies of endocrine cell secretion. In: Endocrinology. 1996 ; Vol. 137, No. 7. pp. 2979-2989.
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