Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1984-10-1
pubmed:abstractText
Mouse spleen suspensions generate discrete cell clusters within 1-2 d of culture. We have isolated these clusters by velocity sedimentation to study their contribution to primary antibody responses. Clusters represent approximately 5% of the starting spleen cells and consist of 20-50% B cells, 20-50% T cells, and 10-20% dendritic cells (DC). When the cultures are stimulated with thymus-dependent antigens, like heterologous red cells or dinitrophenyl-keyhole limpet hemocyanin (DNP-KLH), the clusters are the principal site for the development of plaque-forming cells (PFC). Noncluster fractions form few PFC and only when supplemented with fresh DC. PFC responses in all cases are antigen specific. B cells cluster only in the presence of T cells and DC (1 DC/200 B-T cell mixtures) and only after encountering specific antigen. The elimination of either DC or Lyt-1+2- T cells, with monoclonal antibody and complement, ablates B cell development into PFC. PFC responses are restored with antigen-nonspecific helper factors formed in the syngeneic mixed leukocyte reaction between DC and T cells. Since PFC to DNP-KLH do not develop de novo when B cells are exposed to antigen and helper factors, anti-DNP PFC precursors must be stimulated within clusters to become responsive to helper factors. PFC development within clusters is restricted by the major histocompatibility complex (MHC). When DC and T cells are from strain P1, then P1 but not P2 B cells develop into PFC; when DC are from strain P2 and T cells from strain P1, strain P2 B cells are selected to become PFC in clusters. The entry of B cells into clusters is itself MHC restricted, since P1 DC/T cells aggregate six times as many B cells from strain P1 as strain P2. Thus, clusters are the site in which DC, B, and T cells interact to generate PFC. One can use clusters to retrieve B cells that have been selected in an antigen-dependent, MHC-restricted fashion and to show that clustering B cells become responsive to soluble, polyclonal helper factors.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/6206192-13673134, http://linkedlifedata.com/resource/pubmed/commentcorrection/6206192-14978857, http://linkedlifedata.com/resource/pubmed/commentcorrection/6206192-306408, http://linkedlifedata.com/resource/pubmed/commentcorrection/6206192-4122709, http://linkedlifedata.com/resource/pubmed/commentcorrection/6206192-5355110, http://linkedlifedata.com/resource/pubmed/commentcorrection/6206192-6153679, http://linkedlifedata.com/resource/pubmed/commentcorrection/6206192-6185614, http://linkedlifedata.com/resource/pubmed/commentcorrection/6206192-6227678, http://linkedlifedata.com/resource/pubmed/commentcorrection/6206192-6415207, http://linkedlifedata.com/resource/pubmed/commentcorrection/6206192-6445399, http://linkedlifedata.com/resource/pubmed/commentcorrection/6206192-6475812, http://linkedlifedata.com/resource/pubmed/commentcorrection/6206192-6766981, http://linkedlifedata.com/resource/pubmed/commentcorrection/6206192-6801177, http://linkedlifedata.com/resource/pubmed/commentcorrection/6206192-6966402, http://linkedlifedata.com/resource/pubmed/commentcorrection/6206192-7252426
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0022-1007
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
160
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
858-76
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:6206192-Animals, pubmed-meshheading:6206192-Antibody-Producing Cells, pubmed-meshheading:6206192-B-Lymphocytes, pubmed-meshheading:6206192-Cell Aggregation, pubmed-meshheading:6206192-Epitopes, pubmed-meshheading:6206192-Female, pubmed-meshheading:6206192-Growth Substances, pubmed-meshheading:6206192-H-2 Antigens, pubmed-meshheading:6206192-Hemocyanin, pubmed-meshheading:6206192-Hemolytic Plaque Technique, pubmed-meshheading:6206192-Interleukin-4, pubmed-meshheading:6206192-Lymphocyte Cooperation, pubmed-meshheading:6206192-Lymphokines, pubmed-meshheading:6206192-Male, pubmed-meshheading:6206192-Mice, pubmed-meshheading:6206192-Mice, Inbred A, pubmed-meshheading:6206192-Mice, Inbred C57BL, pubmed-meshheading:6206192-Mice, Inbred ICR, pubmed-meshheading:6206192-Sheep, pubmed-meshheading:6206192-Spleen, pubmed-meshheading:6206192-T-Lymphocytes, Helper-Inducer
pubmed:year
1984
pubmed:articleTitle
Clustering of dendritic cells, helper T lymphocytes, and histocompatible B cells during primary antibody responses in vitro.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't