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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
14
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pubmed:dateCreated |
1991-8-14
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pubmed:abstractText |
We examined the effects of isoproterenol and carbachol on fluid-phase endocytosis by Chinese hamster ovary (CHO) cells transfected with beta-adrenergic, M1, or M3 cholinergic receptors. Isoproterenol increased cAMP production and carbachol increased intracellular Ca, indicating successful expression of the receptor genes and coupling to typical signal transduction pathways. Carbachol inhibited the uptake of horseradish peroxidase (HRP) or Lucifer yellow (markers of fluid-phase endocytosis) in both M1- and M3-containing cells but not in wild-type cells, whereas isoproterenol did not affect pinocytosis in cells transfected with beta-adrenergic receptors. Carbachol inhibited the transit of HRP from an exchangeable pool to a nonexchangeable pool by a latent process requiring minimally 5 min of incubation. During the latent period, only one peak of low-density HRP-containing vesicles was found on Percoll gradients; after 5 min, HRP appeared in both high- and low-density vesicles. Carbachol-treated cells contained less HRP in the high-density fraction enriched in lysosomal markers. Early endosomes from CHO cells labeled for 5 min with HRP underwent fusion to make a more dense population of vesicles in the presence of ATP and KCl at 37 degrees C but not at 4 degrees C. The fused material contained increased levels of G proteins as detected either by ADP ribosylation with appropriate toxins or by immunoblotting with specific antibodies. These findings suggest that GTP binding proteins are internalized in endocytic vesicles and enter into a complex trafficking process involving fusion with other vesicular compartments. Trafficking of endosomes to these compartments is inhibited by activated M1 and M3 muscarinic receptors in CHO cells.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/1906173-1696725,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1906173-1705707,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1906173-1848225,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1906173-2105498,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1906173-2105958,
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http://linkedlifedata.com/resource/pubmed/commentcorrection/1906173-2124972,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1906173-2160830,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1906173-2175603,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1906173-2211876,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1906173-2423023,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1906173-2472400,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1906173-2507534,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1906173-2513326,
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http://linkedlifedata.com/resource/pubmed/commentcorrection/1906173-2538480,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1906173-2555356,
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http://linkedlifedata.com/resource/pubmed/commentcorrection/1906173-942051
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0027-8424
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
88
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
5964-8
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:1906173-Animals,
pubmed-meshheading:1906173-Carbachol,
pubmed-meshheading:1906173-Cell Line,
pubmed-meshheading:1906173-Cricetinae,
pubmed-meshheading:1906173-Cricetulus,
pubmed-meshheading:1906173-Female,
pubmed-meshheading:1906173-GTP-Binding Proteins,
pubmed-meshheading:1906173-Kinetics,
pubmed-meshheading:1906173-Organelles,
pubmed-meshheading:1906173-Ovary,
pubmed-meshheading:1906173-Pinocytosis,
pubmed-meshheading:1906173-Receptors, Muscarinic,
pubmed-meshheading:1906173-Signal Transduction,
pubmed-meshheading:1906173-Transfection
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pubmed:year |
1991
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pubmed:articleTitle |
Carbachol-activated muscarinic (M1 and M3) receptors transfected into Chinese hamster ovary cells inhibit trafficking of endosomes.
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pubmed:affiliation |
Section on Signal Transduction, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709.
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pubmed:publicationType |
Journal Article
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