Literature DB >> 2060645

Native Xenopus oocytes express two types of muscarinic receptors.

A Davidson1, G Mengod, N Matus-Leibovitch, Y Oron.   

Abstract

We have recently described two types of muscarinic responses in native Xenopus oocytes of different donors (common and variant) that display qualitative and quantitative differences (Lupu-Meiri et al., 1990). Here we characterized the muscarinic receptors mediating these two types. The anti-muscarinic toxins from Dentroaspis significantly inhibited responses in oocytes of common donors, but had little effect on responses in oocytes of variant donors, possibly indicating expression of different receptor subtypes. Using specific muscarinic antagonists, we found that oocytes of common donors exhibit a pattern compatible with the M3 subtype of muscarinic receptors, while oocytes of variant donors appear to possess receptors of the M1 subtype. To more directly determine the subtypes of muscarinic receptors in oocytes of both populations of donors, we have microinjected antisense oligonucleotides into native oocytes. Antisense oligonucleotides to unique sequences in the N-terminal and the third cytoplasmic loop of M3 muscarinic receptors caused a significant inhibition of the response of common oocytes, but had virtually no effect on responses in oocytes of variant donors. Conversely, oligonucleotides complementary to the unique sequences of the m1 muscarinic receptors inhibited the response in variant oocytes, but not in oocytes of common donors. We conclude that native Xenopus oocytes of different donors phenotypically express either M3-like (majority) or M1-like (minority) muscarinic receptor subtypes. The differences in receptor subtype expression may explain the different characteristics of responses in the two populations.

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Year:  1991        PMID: 2060645     DOI: 10.1016/0014-5793(91)80697-2

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  9 in total

Review 1.  Synthesis, trafficking, and localization of muscarinic acetylcholine receptors.

Authors:  Neil M Nathanson
Journal:  Pharmacol Ther       Date:  2008-05-16       Impact factor: 12.310

2.  Inositol trisphosphate may access calcium from stores not coupled to muscarinic receptors in Xenopus oocytes.

Authors:  G Goldberg; H Shapira; Y Oron
Journal:  Pflugers Arch       Date:  1992-03       Impact factor: 3.657

3.  Muscarinic receptor heterogeneity in follicle-enclosed Xenopus oocytes.

Authors:  R O Arellano; E Garay; R Miledi
Journal:  J Physiol       Date:  1999-12-01       Impact factor: 5.182

4.  The acetylcholinesterase inhibitor BW284c51 is a potent blocker of Torpedo nicotinic AchRs incorporated into the Xenopus oocyte membrane.

Authors:  Silvia Olivera-Bravo; Isabel Ivorra; Andrés Morales
Journal:  Br J Pharmacol       Date:  2005-01       Impact factor: 8.739

5.  Differential effects of cytoskeletal agents on hemispheric functional expression of cell membrane receptors in Xenopus oocytes.

Authors:  N Matus-Leibovitch; M C Gershengorn; Y Oron
Journal:  Cell Mol Neurobiol       Date:  1993-12       Impact factor: 5.046

6.  Kinetics of the functional loss of different muscarinic receptor isoforms in Xenopus oocytes.

Authors:  N Matus-Leibovitch; G Mengod; Y Oron
Journal:  Biochem J       Date:  1992-08-01       Impact factor: 3.857

7.  A functional role for the two-pore domain potassium channel TASK-1 in cerebellar granule neurons.

Authors:  J A Millar; L Barratt; A P Southan; K M Page; R E Fyffe; B Robertson; A Mathie
Journal:  Proc Natl Acad Sci U S A       Date:  2000-03-28       Impact factor: 11.205

8.  Xenopus laevis RIC-3 enhances the functional expression of the C. elegans homomeric nicotinic receptor, ACR-16, in Xenopus oocytes.

Authors:  Hayley M Bennett; Kristin Lees; Kate M Harper; Andrew K Jones; David B Sattelle; Susan Wonnacott; Adrian J Wolstenholme
Journal:  J Neurochem       Date:  2012-10-10       Impact factor: 5.372

9.  Intercellular communication between follicular angiotensin receptors and Xenopus laevis oocytes: medication by an inositol 1,4,5-trisphosphate-dependent mechanism.

Authors:  K Sandberg; H Ji; T Iida; K J Catt
Journal:  J Cell Biol       Date:  1992-04       Impact factor: 10.539

  9 in total

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