Matches in SemOpenAlex for { <https://semopenalex.org/work/W2116716030> ?p ?o ?g. }
- W2116716030 endingPage "1395" @default.
- W2116716030 startingPage "1385" @default.
- W2116716030 abstract "Sphingosylphosphorylcholine (SPC), or lysophingomyelin, a wide-spectrum growth promoting agent for a variety of cell types (Desai, N. N., and S. Spiegel. 1991. Biochem. Biophys. Res. Comm. 181: 361-366), stimulates cellular proliferation of quiescent Swiss 3T3 fibroblasts to a greater extent than other known growth factors or than the structurally related molecules, sphingosine and sphingosine-1-phosphate. SPC potentiated the mitogenic effect of an activator of protein kinase C, 12-O-tetradecanoylphorbol 13-acetate, and did not compete with phorbol esters for binding to protein kinase C in intact Swiss 3T3 fibroblasts. However, downregulation of protein kinase C, by prolonged treatment with phorbol ester, reduced, but did not eliminate, the ability of SPC to stimulate DNA synthesis, indicating that SPC may act via both protein kinase C-dependent and -independent signaling pathways. SPC induced a rapid rise in intracellular free calcium ([Ca2+]i) in viable 3T3 fibroblasts determined with a digital imaging system. Although the increases in [Ca2+]i were observed even in the absence of calcium in the external medium, no increase in the levels of inositol phosphates could be detected in response to mitogenic concentrations of SPC. Furthermore, in contrast to sphingosine or sphingosine-1-phosphate, the mitogenic effect of SPC was not accompanied by increases in phosphatidic acid levels or changes in cAMP levels. SPC, but not sphingosine or sphingosine-1-phosphate, stimulates the release of arachidonic acid. Therefore, the ability of SPC to act an extremely potent mitogen may be due to activation of signaling pathway(s) distinct from those used by sphingosine or sphingosine-1-phosphate." @default.
- W2116716030 created "2016-06-24" @default.
- W2116716030 creator A5000609206 @default.
- W2116716030 creator A5006668568 @default.
- W2116716030 creator A5014072958 @default.
- W2116716030 creator A5035303261 @default.
- W2116716030 creator A5042538221 @default.
- W2116716030 creator A5071284946 @default.
- W2116716030 creator A5073298233 @default.
- W2116716030 creator A5078822086 @default.
- W2116716030 date "1993-06-15" @default.
- W2116716030 modified "2023-09-27" @default.
- W2116716030 title "Signaling pathways for sphingosylphosphorylcholine-mediated mitogenesis in Swiss 3T3 fibroblasts." @default.
- W2116716030 cites W1493153573 @default.
- W2116716030 cites W1493516959 @default.
- W2116716030 cites W1496978632 @default.
- W2116716030 cites W1508152421 @default.
- W2116716030 cites W1516372175 @default.
- W2116716030 cites W1518225155 @default.
- W2116716030 cites W1518781107 @default.
- W2116716030 cites W1528340834 @default.
- W2116716030 cites W1543411735 @default.
- W2116716030 cites W1548027699 @default.
- W2116716030 cites W1556056622 @default.
- W2116716030 cites W1577542502 @default.
- W2116716030 cites W1579843006 @default.
- W2116716030 cites W1583264261 @default.
- W2116716030 cites W1583807986 @default.
- W2116716030 cites W1591093835 @default.
- W2116716030 cites W16075687 @default.
- W2116716030 cites W1680920356 @default.
- W2116716030 cites W1968500749 @default.
- W2116716030 cites W1974633499 @default.
- W2116716030 cites W1975836015 @default.
- W2116716030 cites W1976588883 @default.
- W2116716030 cites W1978285753 @default.
- W2116716030 cites W1992472345 @default.
- W2116716030 cites W1997093700 @default.
- W2116716030 cites W2002113358 @default.
- W2116716030 cites W2003197672 @default.
- W2116716030 cites W2005069986 @default.
- W2116716030 cites W2008446482 @default.
- W2116716030 cites W2009373735 @default.
- W2116716030 cites W200967821 @default.
- W2116716030 cites W2009993180 @default.
- W2116716030 cites W2014969594 @default.
- W2116716030 cites W2023838194 @default.
- W2116716030 cites W2024905961 @default.
- W2116716030 cites W2027892263 @default.
- W2116716030 cites W2033512750 @default.
- W2116716030 cites W2038590641 @default.
- W2116716030 cites W2043037423 @default.
- W2116716030 cites W2061574494 @default.
- W2116716030 cites W2062595910 @default.
- W2116716030 cites W2063535351 @default.
- W2116716030 cites W2065399078 @default.
- W2116716030 cites W2081916366 @default.
- W2116716030 cites W2084254193 @default.
- W2116716030 cites W2086524338 @default.
- W2116716030 cites W2094032879 @default.
- W2116716030 cites W2096139474 @default.
- W2116716030 cites W2118445198 @default.
- W2116716030 cites W2133404596 @default.
- W2116716030 cites W2149439788 @default.
- W2116716030 cites W2152924742 @default.
- W2116716030 cites W2178760081 @default.
- W2116716030 cites W2218829004 @default.
- W2116716030 cites W2245791631 @default.
- W2116716030 cites W2268425204 @default.
- W2116716030 cites W2414689914 @default.
- W2116716030 cites W47718152 @default.
- W2116716030 cites W83999324 @default.
- W2116716030 doi "https://doi.org/10.1083/jcb.121.6.1385" @default.
- W2116716030 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2119705" @default.
- W2116716030 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/8389770" @default.
- W2116716030 hasPublicationYear "1993" @default.
- W2116716030 type Work @default.
- W2116716030 sameAs 2116716030 @default.
- W2116716030 citedByCount "115" @default.
- W2116716030 countsByYear W21167160302012 @default.
- W2116716030 countsByYear W21167160302014 @default.
- W2116716030 countsByYear W21167160302015 @default.
- W2116716030 countsByYear W21167160302016 @default.
- W2116716030 countsByYear W21167160302022 @default.
- W2116716030 crossrefType "journal-article" @default.
- W2116716030 hasAuthorship W2116716030A5000609206 @default.
- W2116716030 hasAuthorship W2116716030A5006668568 @default.
- W2116716030 hasAuthorship W2116716030A5014072958 @default.
- W2116716030 hasAuthorship W2116716030A5035303261 @default.
- W2116716030 hasAuthorship W2116716030A5042538221 @default.
- W2116716030 hasAuthorship W2116716030A5071284946 @default.
- W2116716030 hasAuthorship W2116716030A5073298233 @default.
- W2116716030 hasAuthorship W2116716030A5078822086 @default.
- W2116716030 hasBestOaLocation W21167160301 @default.
- W2116716030 hasConcept C104317684 @default.
- W2116716030 hasConcept C163235415 @default.
- W2116716030 hasConcept C170493617 @default.
- W2116716030 hasConcept C180899940 @default.