Positive Regulation of Lyn Kinase by CD148 Is Required for B Cell Receptor Signaling in B1 but Not B2 B Cells

Autor: Jing W. Zhu, Katarzyna M. Skrzypczynska, Arthur Weiss
Rok vydání: 2016
Předmět:
0301 basic medicine
Enzyme-Linked Immunospot Assay
Cell
Regulator
Receptor-Like Protein Tyrosine Phosphatases
Lymphocyte Activation
Mice
0302 clinical medicine
hemic and lymphatic diseases
Receptors
Immunology and Allergy
Mice
Knockout

B1 B cell
Kinase
DEP-1
Receptor-Like Protein Tyrosine Phosphatases
Class 3

breakpoint cluster region
BCR
Flow Cytometry
Cell biology
src-Family Kinases
Infectious Diseases
medicine.anatomical_structure
Antigen
030220 oncology & carcinogenesis
CD148
Signal Transduction
Knockout
1.1 Normal biological development and functioning
Immunology
B-cell receptor
B-Lymphocyte Subsets
Receptors
Antigen
B-Cell

Enzyme-Linked Immunosorbent Assay
Biology
T-cell-independent
Article
Ptprj
03 medical and health sciences
Underpinning research
LYN
medicine
Animals
Lyn
B cell
Inflammatory and immune system
B-Cell
Class 3
030104 developmental biology
Pneumovax 23
Cancer research
Zdroj: Immunity, vol 45, iss 6
ISSN: 1074-7613
DOI: 10.1016/j.immuni.2016.10.013
Popis: B1 and B2 B cells differ in their ability to respond to T-cell-independent (TI) antigens. Here we report that the Src-family kinase (SFK) regulator CD148 has a unique and critical role in the initiation of B1 but not B2 cell antigen receptor signaling. CD148 loss-of-function mice were found to have defective B1 B-cell-mediated antibody responses against the T-cell-independent antigens NP-ficoll and Pneumovax 23 and had impaired selection of the B1 B cell receptor (BCR) repertoire. These deficiencies were associated with a decreased ability of B1 B cells to induce BCR signaling downstream of the SFK Lyn. Notably, Lyn appeared to be selectively regulated by CD148 and loss of this SFK resulted in opposite signaling phenotypes in B1 and B2 B cells. These findings reveal that the function and regulation of Lyn during B1 cell BCR signaling is distinct from other B cell subsets.
Databáze: OpenAIRE