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Article ; Online: AKT activity orchestrates marginal zone B cell development in mice and humans

Eva-Maria Cox / Mohamed El-Behi / Stefanie Ries / Johannes F. Vogt / Vivien Kohlhaas / Thomas Michna / Benoît Manfroi / Mona Al-Maarri / Florian Wanke / Boaz Tirosh / Corinne Pondarre / Harry Lezeau / Nir Yogev / Romy Mittenzwei / Marc Descatoire / Sandra Weller / Jean-Claude Weill / Claude-Agnès Reynaud / Pierre Boudinot /
Luc Jouneau / Stefan Tenzer / Ute Distler / Anne Rensing-Ehl / Christoph König / Julian Staniek / Marta Rizzi / Aude Magérus / Frederic Rieux-Laucat / F. Thomas Wunderlich / Nadine Hövelmeyer / Simon Fillatreau

Cell Reports, Vol 42, Iss 4, Pp 112378- (2023)

2023  

Abstract: Summary: The signals controlling marginal zone (MZ) and follicular (FO) B cell development remain incompletely understood. Here, we show that AKT orchestrates MZ B cell formation in mice and humans. Genetic models that increase AKT signaling in B cells ... ...

Abstract Summary: The signals controlling marginal zone (MZ) and follicular (FO) B cell development remain incompletely understood. Here, we show that AKT orchestrates MZ B cell formation in mice and humans. Genetic models that increase AKT signaling in B cells or abolish its impact on FoxO transcription factors highlight the AKT-FoxO axis as an on-off switch for MZ B cell formation in mice. In humans, splenic immunoglobulin (Ig) D+CD27+ B cells, proposed as an MZ B cell equivalent, display higher AKT signaling than naive IgD+CD27− and memory IgD−CD27+ B cells and develop in an AKT-dependent manner from their precursors in vitro, underlining the conservation of this developmental pathway. Consistently, CD148 is identified as a receptor indicative of the level of AKT signaling in B cells, expressed at a higher level in MZ B cells than FO B cells in mice as well as humans.
Keywords CP: Immunology ; CP: Developmental biology ; Biology (General) ; QH301-705.5
Language English
Publishing date 2023-04-01T00:00:00Z
Publisher Elsevier
Document type Article ; Online
Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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