Thymus antibody-secreting cells possess an interferon gene signature and are preferentially expanded in young female mice.

Thymus antibody-secreting cells possess an interferon gene signature and are preferentially expanded in young female mice.
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DOI:
10.1016/j.isci.2023.106223
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发表时间:
2023-03-17
期刊:
影响因子:
5.8
通讯作者:
Pioli, Peter D.
Pioli, Peter D.
中科院分区:
综合性期刊2区
文献类型:
--
作者:
Pioli, KimAnh T.;Lau, Kin H.;Pioli, Peter D.

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Antibody-secreting cells (ASCs) are key contributors to humoral immunity through immunoglobulin production and the potential to be long-lived. ASC persistence has been recognized in the autoimmune thymus (THY); however, only recently has this population been appreciated in healthy THY tissue. We showed that the young female THY was skewed toward higher production of ASCs relative to males. However, these differences disappeared with age. In both sexes, THY ASCs included Ki-67+ plasmablasts which required CD154(CD40L) signals for their propagation. Single cell RNA-sequencing revealed that THY ASCs were enriched for an interferon responsive transcriptional signature relative to those from bone marrow and spleen. Flow cytometry confirmed that THY ASCs had increased levels of Toll-like receptor 7 as well as CD69 and major histocompatibility complex class II. Overall, we identified fundamental aspects of THY ASC biology which may be leveraged for future in depth studies of this population in both health and disease. Thymus ASCs are selectively increased in young female Prdm1-eYFP mice Thymus ASCs contain a CD154(CD40L) dependent Ki-67+ plasmablast population Ectopic in vivo CD40 ligation does not increase total thymus ASC numbers Thymus ASCs possess an interferon responsive gene signature Immunity; Components of the immune system; Cell; Transcriptomics
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