rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
11
|
pubmed:dateCreated |
1990-6-28
|
pubmed:abstractText |
mAb to murine IL-5R were prepared by means of fusion between mouse myeloma cells and spleen cells from a rat immunized with membrane-enriched fractions of IL-5-dependent early B cell line (T88-M). Two mAb (H7 and T21) were selected for their competitive inhibition of receptor binding by 35S-labeled IL-5 and of IL-5 biologic activities. The number of binding sites recognized by the mAb on different cell lines correlated with IL-5 responsiveness. Most surface IgM+ peritoneal B cells were H7+ and more than 70% were also Ly-1(CD5)dull+, and responded to IL-5 for polyclonal IgM production in a high frequency. A significant proportion of splenic B cells reacted with these mAb, although lower number (one-log less) than peritoneal B cells and a small proportion of H7dull+ splenic B cells seems to be Ly-1(CD5)dull+, 1 of 200 splenic B cells responded to IL-5 for IgM production. These results suggest that IL-5R+ B cells may consist of a subpopulation of B cells. Intriguingly, lymphoid populations of bone marrow cells were stained with H7 and T21, whereas myeloid populations were brightly stained with only T21. Finally, both H7 and T21 mAb specifically precipitated a protein of a Mr 60,000 from 125I-labeled cell lysates of IL-5R+ T88-M cells. The IL-5R with similar size (Mr 55,000 to 60,000) was precipitated from the cell lysates of peritoneal B cells. T21 mAb but not H7 mAb precipitated a protein of a Mr 110,000 from the cell lysates of bone marrow cells.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
AIM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD5,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Differentiation,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Ly,
http://linkedlifedata.com/resource/pubmed/chemical/Epitopes,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin M,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-5,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Immunologic,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin-5
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jun
|
pubmed:issn |
0022-1767
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
1
|
pubmed:volume |
144
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
4218-25
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:1692859-Animals,
pubmed-meshheading:1692859-Antibodies, Monoclonal,
pubmed-meshheading:1692859-Antigens, CD5,
pubmed-meshheading:1692859-Antigens, Differentiation,
pubmed-meshheading:1692859-Antigens, Ly,
pubmed-meshheading:1692859-B-Lymphocytes,
pubmed-meshheading:1692859-Binding, Competitive,
pubmed-meshheading:1692859-Bone Marrow Cells,
pubmed-meshheading:1692859-Cell Differentiation,
pubmed-meshheading:1692859-Epitopes,
pubmed-meshheading:1692859-Flow Cytometry,
pubmed-meshheading:1692859-Immunoglobulin M,
pubmed-meshheading:1692859-Interleukin-5,
pubmed-meshheading:1692859-Lymphocyte Activation,
pubmed-meshheading:1692859-Mice,
pubmed-meshheading:1692859-Molecular Weight,
pubmed-meshheading:1692859-Precipitin Tests,
pubmed-meshheading:1692859-Receptors, Immunologic,
pubmed-meshheading:1692859-Receptors, Interleukin,
pubmed-meshheading:1692859-Receptors, Interleukin-5,
pubmed-meshheading:1692859-Spleen
|
pubmed:year |
1990
|
pubmed:articleTitle |
Distribution of IL-5 receptor-positive B cells. Expression of IL-5 receptor on Ly-1(CD5)+ B cells.
|
pubmed:affiliation |
Department of Biology, Kumamoto University Medical School, Japan.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|