May 1990
Volume 31, Issue 5
Free
Articles  |   May 1990
Subcellular distribution of muscarinic acetylcholine receptors in rat exorbital lacrimal gland.
Author Affiliations
  • M E Bradley
    Department of Physiology and Biophysics, University of Southern California School of Medicine, Los Angeles 90033.
  • C L Peters
    Department of Physiology and Biophysics, University of Southern California School of Medicine, Los Angeles 90033.
  • R W Lambert
    Department of Physiology and Biophysics, University of Southern California School of Medicine, Los Angeles 90033.
  • S C Yiu
    Department of Physiology and Biophysics, University of Southern California School of Medicine, Los Angeles 90033.
  • A K Mircheff
    Department of Physiology and Biophysics, University of Southern California School of Medicine, Los Angeles 90033.
Investigative Ophthalmology & Visual Science May 1990, Vol.31, 977-986. doi:
  • Views
  • PDF
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      M E Bradley, C L Peters, R W Lambert, S C Yiu, A K Mircheff; Subcellular distribution of muscarinic acetylcholine receptors in rat exorbital lacrimal gland.. Invest. Ophthalmol. Vis. Sci. 1990;31(5):977-986.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
This content is PDF only. Please click on the PDF icon to access.
Abstract

The muscarinic acetylcholine receptor (MAChR) is an important mediator of parasympathetic regulation of secretion by the rat exorbital lacrimal gland. In order to survey the subcellular distribution of MAChR in lacrimal acinar cells, we have measured the binding of the specific muscarinic cholinergic antagonist [3H]-quinuclidinyl benzilate ([3H]-QNB) to membrane samples isolated from rat exorbital lacrimal glands by differential and equilibrium density gradient centrifugation. Binding of [3H]-QNB in all membrane fractions was consistent with the presence of a single class of receptor which was muscarinic in nature on the basis of its Kd for [3H]-QNB (0.30-0.35 nM) and its ability to interact with the muscarinic agonists carbachol and methachol and the antagonist atropine. MAChR were present at the highest specific activity in acinar cell basal-lateral plasma membrane-derived populations, where Bmax was as high as 1960 fmole/mg protein. However, the density distributions of MAChR and of other membrane markers indicated that the receptors were present also in membranes derived from cytoplasmic structures, where Bmax values ranged from 50.4 to 152.8 fmole/mg protein. Stimulation with 10 microM carbachol for 30 min led to a 20% (P less than 0.05) increase in the relative MAChR content of a population of membranes derived from the acinar cell basal-lateral membrane; an apparent tendency for MAChR activity to decrease in other membrane populations suggests that stimulation might cause a redistribution of MAChR between cytoplasmic pools and the cell surface membranes.

×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×