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Tracing B cell development in human germinal centres by molecular analysis of single cells picked from histological sections.
Author(s) -
Küppers R.,
Zhao M.,
Hansmann M.L.,
Rajewsky K.
Publication year - 1993
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1002/j.1460-2075.1993.tb06189.x
Subject(s) - biology , germinal center , somatic hypermutation , somatic cell , b cell , marginal zone , germline , population , microbiology and biotechnology , follicular dendritic cells , mantle zone , genetics , gene , antibody , t cell , antigen presenting cell , demography , immune system , sociology
Germinal centres are areas of intense B lymphocyte proliferation inside primary B cell follicles in spleen and lymph nodes. Rearranged V genes from single human B cells, isolated from histological sections of two such structures by micromanipulation, were amplified and sequenced. Cells from the follicular mantle were clonally diverse and largely expressed germline V genes. Germinal centres were dominated by a few large B cell clones dispersed throughout these structures and exhibiting intraclonal diversity by ongoing somatic hypermutation. Pronounced counterselection of replacement mutations seen in one of the germinal centres may indicate a late phase of the germinal centre reaction. A polyclonal population of activated B cells expressing unmutated antibodies in the dark zone of the other germinal centre may represent the initial founder cells.

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