Thyrotropin-releasing hormone (TRH) receptor number determines the size of the TRH-responsive phosphoinositide pool. Demonstration using controlled expression of TRH receptors by adenovirus mediated gene transfer

J Biol Chem. 1994 Mar 4;269(9):6779-83.

Abstract

We use an adenovirus vector, AdCMVmTRHR, to express thyrotropin-releasing hormone (TRH) receptors (TRH-Rs) to determine whether the size of the hormone-responsive phosphoinositide pool in mammalian cells is directly related to receptor number. Infection of HeLa cells with increasing numbers of AdCMVmTRHR caused time-dependent graded expression of TRH-Rs. Measurement of cytoplasmic free Ca2+ in individual cells permitted quantitation of the fraction of cells responsive to TRH. Infection with 100 AdCMVmTRHR particles/cell or more led to TRH responsiveness in > or = 90% of HeLa cells. Measurement of prelabeled phosphoinositides hydrolyzed during prolonged TRH stimulation assesses the size of the TRH-responsive pool. In cells infected with AdCMVmTRHR for 24 h, the size of the TRH-responsive phosphoinositide pool increased with increasing TRH-R expression. The TRH-responsive pool also increased with time after infection as the number of TRH-Rs increased. Similar observations were made in GHY and KB cells. These data confirm our previous suggestion (Cubitt, A. B., Geras-Raaka, E., and Gershengorn, M. C. (1990) Biochem. J. 271, 331-336) that there are hormone-responsive and -unresponsive pools of cellular phosphoinositides and that the maximal size of the TRH-responsive pool is directly related to the number of TRH-Rs.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenoviridae
  • Animals
  • Calcium / metabolism*
  • Female
  • Gene Expression
  • Gene Transfer Techniques*
  • Genetic Vectors
  • HeLa Cells
  • Humans
  • KB Cells
  • Kinetics
  • Mammals
  • Phosphatidylinositols / metabolism*
  • Receptors, Thyrotropin-Releasing Hormone / biosynthesis*
  • Receptors, Thyrotropin-Releasing Hormone / physiology*
  • Thyrotropin-Releasing Hormone / pharmacology*
  • Time Factors
  • Uterine Cervical Neoplasms

Substances

  • Phosphatidylinositols
  • Receptors, Thyrotropin-Releasing Hormone
  • Thyrotropin-Releasing Hormone
  • Calcium