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Query: UMLS:C0022672 (
acute tubular necrosis
)
2,175
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Renal ischemia-reperfusion injury (IRI) leads to acute kidney injury or delayed allograft function, which predisposes to fibrosis in the native kidney or kidney transplant. Here we investigated the role of the
signal transducer and activator of transcription 1
(
STAT1
) in inflammatory responses following renal IRI. Our study showed that a subsequent stimulation of Janus-activated kinase 2/
STAT1
and Toll-like receptor 4 pathways led to greater
STAT1
activation followed by increased cytokine transcription compared with single-pathway stimulation in murine renal tubular cells. Moreover, we observed increased activation of
STAT1
under hypoxic conditions. In vivo,
STAT1
-/-
mice displayed less
acute tubular necrosis
and decreased macrophage infiltration 24 h after renal ischemia. However, investigation of the healing phase (30 days after IRI) revealed significantly more fibrosis in
STAT1
-/-
than in wild-type kidneys. In addition, we demonstrated increased macrophage infiltration in
STAT1
-/-
kidneys. Flow cytometry analysis revealed that
STAT1
deficiency drives an alternatively activated macrophage phenotype, which is associated with downregulated cluster of differentiation 80 expression, decreased intracellular reactive oxygen species production, and enhanced ability for phagocytosis. Furthermore, we detected immunohistochemically enhanced
STAT1
expression in human renal allograft biopsies with no interstitial fibrosis/tubular atrophy (IF/TA) compared with specimens with severe IF/TA without specific etiology. Thus,
STAT1
activation drives macrophages toward an alternatively activated phenotype and enhances fibrogenesis indicating a potential
STAT1
-driven protective mechanism in tissue repair after ischemic injury.
...
PMID:STAT1 regulates macrophage number and phenotype and prevents renal fibrosis after ischemia-reperfusion injury. 3040 64