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MicroRNAs prevent the generation of autoreactive antibodies

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25 de November de 2010/in Belver's Lab/by miguel

Immunity. 2010 Nov 24;33(5):713-22. doi: 10.1016/j.immuni.2010.11.010.

ABSTRACT

MicroRNAs have been shown to be critical for a number of aspects of immune system regulation and function. Here, we have examined the role of microRNAs in terminal B cell differentiation by analyzing Cd19-Cre(ki/+) Dicer1(fl/fl) mice. We found that in the absence of Dicer, the transitional and marginal zone (MZ) B cell compartments were overrepresented and follicular (FO) B cell generation was impaired. microRNA analysis revealed that miR185, a microRNA overexpressed in FO cells, dampened B cell receptor (BCR) signaling through Bruton tyrosine kinase downregulation. Dicer-deficient B cells had a skewed BCR repertoire with hallmarks of autoreactivity, which correlated with high titers of autoreactive antibodies in serum and autoimmune features in females. Together, our results reveal a crucial role for microRNAs in late B cell differentiation and in the establishment of B cell tolerance.

PMID:21093320 | PMC:PMC3687137 | DOI:10.1016/j.immuni.2010.11.010

https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg 0 0 miguel https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg miguel2010-11-25 11:00:002010-11-25 11:00:00MicroRNAs prevent the generation of autoreactive antibodies

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