Carbachol induces secretion in a mast cell line (RBL-2H3) transfected with the ml muscarinic receptor gene

The possibility that the ml muscarinic receptor subtype can induce release of intracellular granules and transmitters was studied by transfecting a cultured mast cell line, RBL-2H3 cells, with the ml receptor gene. Comparisons were made between carbachol- and antigen-induced activation of various se...

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Veröffentlicht in:FEBS letters 1991-09, Vol.289 (1), p.47-50
Hauptverfasser: Jones, S.V.Penelope, Choi, Oksoon H., Beaven, Michael A.
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Choi, Oksoon H.
Beaven, Michael A.
description The possibility that the ml muscarinic receptor subtype can induce release of intracellular granules and transmitters was studied by transfecting a cultured mast cell line, RBL-2H3 cells, with the ml receptor gene. Comparisons were made between carbachol- and antigen-induced activation of various secretory responses. Like antigen, carbachol stimulated inositol phospholipid hydrolysis and release of arachidonic acid with concomitant dose-dependent secretion of granular contents. Carbachol also stimulated a biphasic increase in intracellular calcium, as measured by single cell fura-2 measurements. Although the kinetics of the carbachol-induced rise in intracellular calcium differed from that induced by antigen, they both utilized the same intracellular pool of calcium, and the second phase of the rise in intracellular calcium was dependent on extracellular calcium in both cases. Thus, the ml muscarinic receptor activates release of granules by a mechanism ostensibly similar to that of antigen.
doi_str_mv 10.1016/0014-5793(91)80905-I
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Comparisons were made between carbachol- and antigen-induced activation of various secretory responses. Like antigen, carbachol stimulated inositol phospholipid hydrolysis and release of arachidonic acid with concomitant dose-dependent secretion of granular contents. Carbachol also stimulated a biphasic increase in intracellular calcium, as measured by single cell fura-2 measurements. Although the kinetics of the carbachol-induced rise in intracellular calcium differed from that induced by antigen, they both utilized the same intracellular pool of calcium, and the second phase of the rise in intracellular calcium was dependent on extracellular calcium in both cases. Thus, the ml muscarinic receptor activates release of granules by a mechanism ostensibly similar to that of antigen.</description><identifier>ISSN: 0014-5793</identifier><identifier>EISSN: 1873-3468</identifier><identifier>DOI: 10.1016/0014-5793(91)80905-I</identifier><identifier>PMID: 1832647</identifier><identifier>CODEN: FEBLAL</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>[Ca2+]i ; acetylcholine ; Aminoquinolines ; Animals ; Antigens - pharmacology ; Arachidonic Acid ; Arachidonic Acids - metabolism ; beta-N-Acetylhexosaminidases - metabolism ; Biological and medical sciences ; Calcium - metabolism ; carbachol ; Carbachol - pharmacology ; Cell Line ; Cell physiology ; Cloned ml muscarinic receptor ; concentration of free cytosolic Ca2 ; dinitrophenylated bovine serum albumin ; DNP-BSA ; EGTA ; ethylene glycol-bis-(β aminoethylether) N,N,N′N′-tetraacetic acid ; Exocytosis ; Expression (RBL-2H3 cell) ; Fluorescent Dyes ; Fundamental and applied biological sciences. Psychology ; Hydrolysis ; IgE ; immunoglobulin E ; Inositol Phosphates - metabolism ; Intracellular signal ; Mast Cells - metabolism ; Molecular and cellular biology ; Phospholipids - metabolism ; Rats ; Receptors, Muscarinic - genetics ; Receptors, Muscarinic - metabolism ; Secretion. 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Comparisons were made between carbachol- and antigen-induced activation of various secretory responses. Like antigen, carbachol stimulated inositol phospholipid hydrolysis and release of arachidonic acid with concomitant dose-dependent secretion of granular contents. Carbachol also stimulated a biphasic increase in intracellular calcium, as measured by single cell fura-2 measurements. Although the kinetics of the carbachol-induced rise in intracellular calcium differed from that induced by antigen, they both utilized the same intracellular pool of calcium, and the second phase of the rise in intracellular calcium was dependent on extracellular calcium in both cases. Thus, the ml muscarinic receptor activates release of granules by a mechanism ostensibly similar to that of antigen.</description><subject>[Ca2+]i</subject><subject>acetylcholine</subject><subject>Aminoquinolines</subject><subject>Animals</subject><subject>Antigens - pharmacology</subject><subject>Arachidonic Acid</subject><subject>Arachidonic Acids - metabolism</subject><subject>beta-N-Acetylhexosaminidases - metabolism</subject><subject>Biological and medical sciences</subject><subject>Calcium - metabolism</subject><subject>carbachol</subject><subject>Carbachol - pharmacology</subject><subject>Cell Line</subject><subject>Cell physiology</subject><subject>Cloned ml muscarinic receptor</subject><subject>concentration of free cytosolic Ca2</subject><subject>dinitrophenylated bovine serum albumin</subject><subject>DNP-BSA</subject><subject>EGTA</subject><subject>ethylene glycol-bis-(β aminoethylether) N,N,N′N′-tetraacetic acid</subject><subject>Exocytosis</subject><subject>Expression (RBL-2H3 cell)</subject><subject>Fluorescent Dyes</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hydrolysis</subject><subject>IgE</subject><subject>immunoglobulin E</subject><subject>Inositol Phosphates - metabolism</subject><subject>Intracellular signal</subject><subject>Mast Cells - metabolism</subject><subject>Molecular and cellular biology</subject><subject>Phospholipids - metabolism</subject><subject>Rats</subject><subject>Receptors, Muscarinic - genetics</subject><subject>Receptors, Muscarinic - metabolism</subject><subject>Secretion. 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Psychology</topic><topic>Hydrolysis</topic><topic>IgE</topic><topic>immunoglobulin E</topic><topic>Inositol Phosphates - metabolism</topic><topic>Intracellular signal</topic><topic>Mast Cells - metabolism</topic><topic>Molecular and cellular biology</topic><topic>Phospholipids - metabolism</topic><topic>Rats</topic><topic>Receptors, Muscarinic - genetics</topic><topic>Receptors, Muscarinic - metabolism</topic><topic>Secretion. Exocytosis</topic><topic>Transfection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jones, S.V.Penelope</creatorcontrib><creatorcontrib>Choi, Oksoon H.</creatorcontrib><creatorcontrib>Beaven, Michael A.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>FEBS letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jones, S.V.Penelope</au><au>Choi, Oksoon H.</au><au>Beaven, Michael A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Carbachol induces secretion in a mast cell line (RBL-2H3) transfected with the ml muscarinic receptor gene</atitle><jtitle>FEBS letters</jtitle><addtitle>FEBS Lett</addtitle><date>1991-09-02</date><risdate>1991</risdate><volume>289</volume><issue>1</issue><spage>47</spage><epage>50</epage><pages>47-50</pages><issn>0014-5793</issn><eissn>1873-3468</eissn><coden>FEBLAL</coden><abstract>The possibility that the ml muscarinic receptor subtype can induce release of intracellular granules and transmitters was studied by transfecting a cultured mast cell line, RBL-2H3 cells, with the ml receptor gene. Comparisons were made between carbachol- and antigen-induced activation of various secretory responses. Like antigen, carbachol stimulated inositol phospholipid hydrolysis and release of arachidonic acid with concomitant dose-dependent secretion of granular contents. Carbachol also stimulated a biphasic increase in intracellular calcium, as measured by single cell fura-2 measurements. Although the kinetics of the carbachol-induced rise in intracellular calcium differed from that induced by antigen, they both utilized the same intracellular pool of calcium, and the second phase of the rise in intracellular calcium was dependent on extracellular calcium in both cases. Thus, the ml muscarinic receptor activates release of granules by a mechanism ostensibly similar to that of antigen.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>1832647</pmid><doi>10.1016/0014-5793(91)80905-I</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Elsevier ScienceDirect Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects [Ca2+]i
acetylcholine
Aminoquinolines
Animals
Antigens - pharmacology
Arachidonic Acid
Arachidonic Acids - metabolism
beta-N-Acetylhexosaminidases - metabolism
Biological and medical sciences
Calcium - metabolism
carbachol
Carbachol - pharmacology
Cell Line
Cell physiology
Cloned ml muscarinic receptor
concentration of free cytosolic Ca2
dinitrophenylated bovine serum albumin
DNP-BSA
EGTA
ethylene glycol-bis-(β aminoethylether) N,N,N′N′-tetraacetic acid
Exocytosis
Expression (RBL-2H3 cell)
Fluorescent Dyes
Fundamental and applied biological sciences. Psychology
Hydrolysis
IgE
immunoglobulin E
Inositol Phosphates - metabolism
Intracellular signal
Mast Cells - metabolism
Molecular and cellular biology
Phospholipids - metabolism
Rats
Receptors, Muscarinic - genetics
Receptors, Muscarinic - metabolism
Secretion. Exocytosis
Transfection
title Carbachol induces secretion in a mast cell line (RBL-2H3) transfected with the ml muscarinic receptor gene
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