Polyclonal immunoglobulin response of thymic, hepatic and splenic lymphocytes from fetal, germ-free and conventionally reared pigs to different B-cell activators
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
8763157
DOI
10.1007/bf02814751
Knihovny.cz E-resources
- MeSH
- Lymphocyte Activation * MeSH
- B-Lymphocytes drug effects immunology MeSH
- Bacterial Proteins * MeSH
- Chaperonin 60 MeSH
- Chaperonins immunology MeSH
- Enzyme-Linked Immunosorbent Assay MeSH
- Germ-Free Life immunology MeSH
- Liver cytology embryology growth & development immunology MeSH
- Lipopolysaccharides immunology MeSH
- Pokeweed Mitogens immunology MeSH
- Mitogens immunology MeSH
- Organic Chemicals MeSH
- Organ Culture Techniques MeSH
- Fetus immunology MeSH
- Swine embryology growth & development immunology MeSH
- Spleen cytology immunology MeSH
- Thymus Gland cytology embryology growth & development immunology MeSH
- Antibody Formation * MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Bacterial Proteins * MeSH
- Chaperonin 60 MeSH
- Chaperonins MeSH
- heat-shock protein 65, Mycobacterium MeSH Browser
- Lipopolysaccharides MeSH
- Pokeweed Mitogens MeSH
- Mitogens MeSH
- Nocardia delipidated cell mitogen MeSH Browser
- Organic Chemicals MeSH
Immunoglobulin (Ig) response to different polyclonal B-cell activators was measured by ELISA in cell culture media of thymocytes, splenocytes and liver cells isolated from pig fetuses, 8-d-old germ-free piglets and conventionally reared pigs. Both in fetal and in postnatal life polyclonally stimulated lymphocytes were found to produce predominantly the IgM isotype; the first IgM formation was detected in 50-d-old fetal liver (gestation in pigs lasts 114 d). Surprisingly, 73-d-old fetal thymic cells were shown to be induced to Ig synthesis and secretion. In contrast to splenocytes of the same age, which secreted exclusively IgM, fetal thymocytes produced IgM, IgG and IgA. Polyclonally stimulated splenic cells as compared with thymic cells started to produce IgA later in fetal ontogeny, whereas the IgG response was not detectable in splenic cell culture media during the whole embryonal development and appeared only after birth. The earliest and the highest Ig stimulation was found after cultivation of lymphocytes with Nocardia delipidated cell mitogen. Interestingly, the moderate stimulatory effect of 65-kDa heat shock protein (Hsp-65) in polyclonal IgM response of fetal splenocytes was observed. We showed that thymic B lymphocytes represent probably the first maturing B cell population detectable in fetal life, which is able to differentiate after polyclonal stimulation into IgM as well as IgA and IgG producing cells.
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