The transcription factor Hhex cooperates with the corepressor Tle3 to promote memory B cell development

Brian J. Laidlaw, Lihui Duan, Ying Xu, Sara E. Vazquez, Jason G. Cyster

Research output: Contribution to journalArticlepeer-review

31 Scopus citations

Abstract

Memory B cells (MBCs) are essential for long-lived humoral immunity. However, the transcription factors involved in MBC differentiation are poorly defined. Here, using single-cell RNA sequencing analysis, we identified a population of germinal center (GC) B cells in the process of differentiating into MBCs. Using an inducible CRISPR–Cas9 screening approach, we identified the hematopoietically expressed homeobox protein Hhex as a transcription factor regulating MBC differentiation. The corepressor Tle3 was also identified in the screen and was found to interact with Hhex to promote MBC development. Bcl-6 directly repressed Hhex in GC B cells. Reciprocally, Hhex-deficient MBCs exhibited increased Bcl6 expression and reduced expression of the Bcl-6 target gene Bcl2. Overexpression of Bcl-2 was able to rescue MBC differentiation in Hhex-deficient cells. We also identified Ski as an Hhex-induced transcription factor involved in MBC differentiation. These findings establish an important role for Hhex–Tle3 in regulating the transcriptional circuitry governing MBC differentiation.

Original languageEnglish
Pages (from-to)1082-1093
Number of pages12
JournalNature immunology
Volume21
Issue number9
DOIs
StatePublished - Sep 1 2020

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