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Altered Phenotype and Enhanced Antibody-Producing Ability of Peripheral B Cells in Mice with Cd19-Driven Cre Expression.
Zhao, Ying; Zhao, Sai; Qin, Xiao-Yuan; He, Ting-Ting; Hu, Miao-Miao; Gong, Zheng; Wang, Hong-Min; Gong, Fang-Yuan; Gao, Xiao-Ming; Wang, Jun.
Afiliación
  • Zhao Y; Department of Pathophysiology, School of Biology and Basic Medical Sciences, Soochow University, Suzhou 215123, China.
  • Zhao S; Institutes of Biology and Medical Sciences, Soochow University, Suzhou 215123, China.
  • Qin XY; Institutes of Biology and Medical Sciences, Soochow University, Suzhou 215123, China.
  • He TT; Institutes of Biology and Medical Sciences, Soochow University, Suzhou 215123, China.
  • Hu MM; Institutes of Biology and Medical Sciences, Soochow University, Suzhou 215123, China.
  • Gong Z; Institutes of Biology and Medical Sciences, Soochow University, Suzhou 215123, China.
  • Wang HM; Institutes of Biology and Medical Sciences, Soochow University, Suzhou 215123, China.
  • Gong FY; Institutes of Biology and Medical Sciences, Soochow University, Suzhou 215123, China.
  • Gao XM; Institutes of Biology and Medical Sciences, Soochow University, Suzhou 215123, China.
  • Wang J; Institutes of Biology and Medical Sciences, Soochow University, Suzhou 215123, China.
Cells ; 11(4)2022 02 16.
Article en En | MEDLINE | ID: mdl-35203346
Given the importance of B lymphocytes in inflammation and immune defense against pathogens, mice transgenic for Cre under the control of Cd19 promoter (Cd19Cre/+ mice) have been widely used to specifically investigate the role of loxP-flanked genes in B cell development/function. However, impacts of expression/insertion of the Cre transgene on the phenotype and function of B cells have not been carefully studied. Here, we show that the number of marginal zone B and B1a cells was selectively reduced in Cd19Cre/+ mice, while B cell development in the bone marrow and total numbers of peripheral B cells were comparable between Cd19Cre/+ and wild type C57BL/6 mice. Notably, humoral responses to both T cell-dependent and independent antigens were significantly increased in Cd19Cre/+ mice. We speculate that these differences are mainly attributable to reduced surface CD19 levels caused by integration of the Cre-expressing cassette that inactivates one Cd19 allele. Moreover, our literature survey showed that expression of Cd19Cre/+ alone may affect the development/progression of inflammatory and anti-infectious responses. Thus, our results have important implications for the design and interpretation of results on gene functions specifically targeted in B cells in the Cd19Cre/+ mouse strain, for instance, in the context of (auto) inflammatory/infectious diseases.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Linfocitos B / Antígenos CD19 Límite: Animals Idioma: En Revista: Cells Año: 2022 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Linfocitos B / Antígenos CD19 Límite: Animals Idioma: En Revista: Cells Año: 2022 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza