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Plexin B2 and Semaphorin 4C Guide T Cell Recruitment and Function in the Germinal Center
Author(s) -
Hu Yan,
Longyan Wu,
Changming Shih,
Shiyue Hou,
Jingwen Shi,
Tianyang Mao,
Wenbin Chen,
Bhavani Melvin,
Robert J. Rigby,
Yingjia Chen,
Haochen Jiang,
Roland H. Friedel,
Carola G. Vinuesa,
Hai Qi
Publication year - 2017
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2017.04.022
Subject(s) - germinal center , semaphorin , biology , transmembrane protein , microbiology and biotechnology , receptor , plexin , function (biology) , b cell , antibody , immunology , genetics
Follicular T helper (T FH ) cells orchestrate the germinal center (GC) response locally. T FH localization in GCs is controlled by chemo-guidance cues and antigen-specific adhesion. Here. we define an antigen-independent, contact-dependent, adhesive guidance system for T FH cells. Unusual for amoeboid cell migration, the system is composed of transmembrane plexin B2 (PlxnB2) molecule, which is highly expressed by GC B cells, and its transmembrane binding partner semaphorin 4C (Sema4C), which is upregulated on T FH cells. Sema4C on T FH cells serves as a receptor to sense the GC-presented PlxnB2 cue and biases T FH migration inwards at the GC edge to promote GC access. The absence of PlxnB2 from the GC or Sema4C from T FH cells causes T FH accumulation along the GC border, impairs T-B cell interactions in the GC, and is associated with defective plasma cell production and affinity maturation. Therefore, Sema4C and PlxnB2 regulate GC T FH recruitment and function and optimize antibody responses.

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