Abnormal B lymphocyte development and autoimmunity in hypoxia-inducible factor 1α-deficient chimeric mice

H Kojima, H Gu, S Nomura… - Proceedings of the …, 2002 - National Acad Sciences
H Kojima, H Gu, S Nomura, CC Caldwell, T Kobata, P Carmeliet, GL Semenza, MV Sitkovsky
Proceedings of the National Academy of Sciences, 2002National Acad Sciences
Immune cells are exposed to low oxygen tensions as they develop and migrate between
blood and different tissues, but the mechanisms by which lymphocytes adapt to hypoxia are
poorly understood. Studies reported here of hypoxia-inducible factor 1α (HIF-1α) in
lymphocyte development and functions suggest that it has a critical role in regulation of
these processes. HIF-1α deficiency in Hif1α−/−→ Rag2−/− chimeric mice results in dramatic
and cell lineage-specific defects, which include appearance of abnormal peritoneal B-1-like …
Immune cells are exposed to low oxygen tensions as they develop and migrate between blood and different tissues, but the mechanisms by which lymphocytes adapt to hypoxia are poorly understood. Studies reported here of hypoxia-inducible factor 1α (HIF-1α) in lymphocyte development and functions suggest that it has a critical role in regulation of these processes. HIF-1α deficiency in Hif1α−/−Rag2−/− chimeric mice results in dramatic and cell lineage-specific defects, which include appearance of abnormal peritoneal B-1-like lymphocytes, with high expression of B220 (CD45) receptor-associated protein tyrosine phosphatase and autoimmunity (accumulation of anti-dsDNA antibodies and rheumatoid factor in serum, deposits of IgG and IgM in kidney and proteinuria) as well as distortions of maturation of B-2 lymphocytes in bone marrow.
National Acad Sciences