Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
2010-9-22
pubmed:abstractText
Ischemia/reperfusion (I/R) triggers a robust inflammatory response within the kidney. Numerous components of the immune system contribute to the resultant renal injury, including the complement system. We sought to identify whether natural Abs bind to the postischemic kidney and contribute to complement activation after I/R. We depleted peritoneal B cells in mice by hypotonic shock. Depletion of the peritoneal B cells prevented the deposition of IgM within the glomeruli after renal I/R and attenuated renal injury after I/R. We found that glomerular IgM activates the classical pathway of complement, but it does not cause substantial deposition of C3 within the kidney. Furthermore, mice deficient in classical pathway proteins were not protected from injury, indicating that glomerular IgM does not cause injury through activation of the classical pathway. We also subjected mice deficient in all mature B cells (?MT mice) to renal I/R and found that they sustained worse renal injury than wild-type controls. Serum IL-10 levels were lower in the ?MT mice. Taken together, these results indicate that natural Ab produced by peritoneal B cells binds within the glomerulus after renal I/R and contributes to functional renal injury. However, nonperitoneal B cells attenuate renal injury after I/R, possibly through the production of IL-10.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/20810984-10066708, http://linkedlifedata.com/resource/pubmed/commentcorrection/20810984-10811844, http://linkedlifedata.com/resource/pubmed/commentcorrection/20810984-11737586, http://linkedlifedata.com/resource/pubmed/commentcorrection/20810984-11788450, http://linkedlifedata.com/resource/pubmed/commentcorrection/20810984-12165541, http://linkedlifedata.com/resource/pubmed/commentcorrection/20810984-12538716, http://linkedlifedata.com/resource/pubmed/commentcorrection/20810984-12960350, http://linkedlifedata.com/resource/pubmed/commentcorrection/20810984-15253693, http://linkedlifedata.com/resource/pubmed/commentcorrection/20810984-15749852, http://linkedlifedata.com/resource/pubmed/commentcorrection/20810984-15849610, http://linkedlifedata.com/resource/pubmed/commentcorrection/20810984-15882434, http://linkedlifedata.com/resource/pubmed/commentcorrection/20810984-16444293, http://linkedlifedata.com/resource/pubmed/commentcorrection/20810984-17064966, http://linkedlifedata.com/resource/pubmed/commentcorrection/20810984-17113913, http://linkedlifedata.com/resource/pubmed/commentcorrection/20810984-18568640, http://linkedlifedata.com/resource/pubmed/commentcorrection/20810984-18759928, http://linkedlifedata.com/resource/pubmed/commentcorrection/20810984-8524789, http://linkedlifedata.com/resource/pubmed/commentcorrection/20810984-9590289
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
1550-6606
pubmed:author
pubmed:issnType
Electronic
pubmed:day
1
pubmed:volume
185
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4393-400
pubmed:dateRevised
2011-9-26
pubmed:meshHeading
pubmed:year
2010
pubmed:articleTitle
B cell subsets contribute to renal injury and renal protection after ischemia/reperfusion.
pubmed:affiliation
Department of Medicine, University of Colorado Denver School of Medicine, Denver, CO 80045, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural