Akt1 and Akt2 promote peripheral B-cell maturation and survival

Although the 3 isoforms of Akt regulate cell growth, proliferation, and survival in a wide variety of cell types, their role in B-cell development is unknown. We assessed B-cell maturation in the bone marrow (BM) and periphery in chimeras established with fetal liver progenitors lacking Akt1 and/or...

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Veröffentlicht in:Blood 2010-05, Vol.115 (20), p.4043-4050
Hauptverfasser: Calamito, Marco, Juntilla, Marisa M., Thomas, Matthew, Northrup, Daniel L., Rathmell, Jeffrey, Birnbaum, Morris J., Koretzky, Gary, Allman, David
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Sprache:eng
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Zusammenfassung:Although the 3 isoforms of Akt regulate cell growth, proliferation, and survival in a wide variety of cell types, their role in B-cell development is unknown. We assessed B-cell maturation in the bone marrow (BM) and periphery in chimeras established with fetal liver progenitors lacking Akt1 and/or Akt2. We found that the generation of marginal zone (MZ) and B1 B cells, 2 key sources of antibacterial antibodies, was highly dependent on the combined expression of Akt1 and Akt2. In contrast, Akt1/2 deficiency did not negatively affect the generation of transitional or mature follicular B cells in the periphery or their precursors in the BM. However, Akt1/2-deficient follicular B cells exhibited a profound survival defect when forced to compete against wild-type B cells in vivo. Altogether, these studies show that Akt signaling plays a key role in peripheral B-cell maturation and survival.
ISSN:0006-4971
1528-0020
DOI:10.1182/blood-2009-09-241638