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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0003241,
umls-concept:C0024264,
umls-concept:C0025402,
umls-concept:C0038734,
umls-concept:C0205198,
umls-concept:C0220781,
umls-concept:C0439849,
umls-concept:C0441712,
umls-concept:C0445223,
umls-concept:C0591833,
umls-concept:C1280500,
umls-concept:C1533691,
umls-concept:C1552599,
umls-concept:C1704787,
umls-concept:C1752930,
umls-concept:C1879547,
umls-concept:C1883254
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pubmed:issue |
4
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pubmed:dateCreated |
1982-4-12
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pubmed:abstractText |
Seven thiol compounds, namely, 2-mercaptoethanol (2-ME), alpha -thioglycerol (alpha -TG), dithiothreitol (DTT), cysteamine, L-cysteine (Cys), glutathione (GSH), and sodium thioglycollate (TGL) were examined for their mitogenic activities, the effects on mitogen-induced 3H-thymidine uptake, and the effects on antibody synthesis in vitro in murine spleen lymphocytes. All these thiols showed mitogenic activities in RPMI-1640 medium containing 10% fetal calf serum (FCS) with the following order of effectiveness: 2-ME greater than or equal to alpha -TG greater than DTT greater than cysteamine greater than Cys greater than or equal to GSH greater than TGL. A close correlation was observed between the enhancement of the response to lipopolysaccharide (LPS) and the mitogenic activities of these thiol compounds in their magnitude and dose-response profiles. The primary antibody response in vitro to sheep red blood cells (SRBC) (thymus-dependent) or dinitrophenyl (DNP)-Ficoll (thymus-independent) was augmented in a similar fashion by these compounds. T-cells depletion did not influence the enhancement by 2-ME of the antibody response to DNP-Ficoll. There was a discrepancy between the dose-response profiles of mitogenic activities of these compounds and their augmenting effects on antibody responses. Particularly, 2-ME and DTT significantly enhanced the antibody response to DNP-Ficoll or SRBC even at the nonmitogenic doses. Ethyl mercaptan (HSCH2 CH3) showed similar activities to 2-ME, but methylthioethanol (CH3 SCH2 CH2 OH) and ethanol (CH3 CH2 OH) were inactive, thus indicating that the thiol group would play an essential role in the above activities of 2-ME.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0162-3109
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
3
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
333-45
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pubmed:dateRevised |
2003-11-14
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pubmed:meshHeading |
pubmed-meshheading:6976954-Animals,
pubmed-meshheading:6976954-Antibody Formation,
pubmed-meshheading:6976954-B-Lymphocytes,
pubmed-meshheading:6976954-Cell Division,
pubmed-meshheading:6976954-Female,
pubmed-meshheading:6976954-Mercaptoethanol,
pubmed-meshheading:6976954-Mice,
pubmed-meshheading:6976954-Mice, Inbred BALB C,
pubmed-meshheading:6976954-Mitogens,
pubmed-meshheading:6976954-Spleen,
pubmed-meshheading:6976954-Stimulation, Chemical,
pubmed-meshheading:6976954-Sulfhydryl Compounds,
pubmed-meshheading:6976954-T-Lymphocytes
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pubmed:year |
1981
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pubmed:articleTitle |
Activation of murine lymphocytes by 2-mercaptoethanol and related thiol compounds and its mechanism. I. Relationship between mitogenic activities and augmenting effects on antibody synthesis in vitro.
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pubmed:publicationType |
Journal Article
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