Literature DB >> 18827964

Contribution of T lymphocytes to rat renal ischemia/reperfusion injury.

Eisei Noiri1, Kent Doi, Reiko Inagi, Masaomi Nangaku, Toshiro Fujita.   

Abstract

BACKGROUND: This study aimed to elucidate the early involvement of T lymphocytes in renal ischemia/reperfusion injury.
METHODS: Athymic nude rats (F344/N_Jcl-nu) and control F344/Jcl were subjected to 45 min unilateral renal ischemia. To determine whether the observed differences might be derived from the T lymphocyte presence, T lymphocytes from the spleens of F344/Jcl were injected into F344/N_Jcl-nu via tail vein at the initiation of reperfusion. Immunohistochemical analysis was performed for CD3, the proliferative cell nuclear antigen (PCNA), vimentin, and E-cadherin. T lymphocytes were obtained from the green fluorescent protein transgenic (GFP) rats, and transplanted to F344/N_Jcl-nu 10 min before reperfusion. The animals were euthanized 15 min after reperfusion.
RESULTS: F344/N_Jcl-nu showed less retention of both Cr and BUN at 24 and 48 h after reperfusion, compared with F344/Jcl. F344/N_Jcl-nu received T lymphocyte transplantation showed significantly higher retention of both Cr and BUN 24, 48, and 72 h after reperfusion than those without T lymphocyte. A rapid infiltration of T lymphocytes into proximal tubular epithelial cells and tubular lumen was observed using T lymphocytes with green fluorescent protein. In contrast, T lymphocytes were observed with much less frequency 24 h after ischemia. The number of PCNA-positive proximal tubular cells 24 h after the initiation of reperfusion was significantly smaller in the T lymphocyte transplantation group compared with the non-transplantation group. The vimentin positivity and cytoplasmic staining of E-cadherin were also more prominent in the transplantation group.
CONCLUSION: These findings demonstrate a rapid renal T lymphocyte infiltration, which propagate renal functional deterioration.

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Year:  2008        PMID: 18827964     DOI: 10.1007/s10157-008-0082-1

Source DB:  PubMed          Journal:  Clin Exp Nephrol        ISSN: 1342-1751            Impact factor:   2.801


  27 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2000-01-18       Impact factor: 11.205

2.  Antithrombin reduces ischemia/reperfusion-induced renal injury in rats by inhibiting leukocyte activation through promotion of prostacyclin production.

Authors:  Akio Mizutani; Kenji Okajima; Mitsuhiro Uchiba; Hirotaka Isobe; Naoaki Harada; Sachiko Mizutani; Takayuki Noguchi
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4.  Monocyte chemoattractant protein-1 expression correlates with monocyte infiltration in the post-ischemic kidney.

Authors:  James C Rice; Jeff S Spence; Deborah L Yetman; Robert L Safirstein
Journal:  Ren Fail       Date:  2002-11       Impact factor: 2.606

5.  ICAM-1 expression and leukocyte accumulation in inner stripe of outer medulla in early phase of ischemic compared to HgCl2-induced ARF.

Authors:  Kathleen E De Greef; Dirk K Ysebaert; Veerle Persy; Sven R Vercauteren; Marc E De Broe
Journal:  Kidney Int       Date:  2003-05       Impact factor: 10.612

6.  Oxidative and nitrosative stress in acute renal ischemia.

Authors:  E Noiri; A Nakao; K Uchida; H Tsukahara; M Ohno; T Fujita; S Brodsky; M S Goligorsky
Journal:  Am J Physiol Renal Physiol       Date:  2001-11

7.  Postischemic renal injury is mediated by neutrophils and leukotrienes.

Authors:  J M Klausner; I S Paterson; G Goldman; L Kobzik; C Rodzen; R Lawrence; C R Valeri; D Shepro; H B Hechtman
Journal:  Am J Physiol       Date:  1989-05

8.  Enhanced MCP-1 expression during ischemia/reperfusion injury is mediated by oxidative stress and NF-kappaB.

Authors:  Fion L Sung; Tong Y Zhu; Kathy K W Au-Yeung; Yaw L Siow; Karmin O
Journal:  Kidney Int       Date:  2002-10       Impact factor: 10.612

9.  New member of the winged-helix protein family disrupted in mouse and rat nude mutations.

Authors:  M Nehls; D Pfeifer; M Schorpp; H Hedrich; T Boehm
Journal:  Nature       Date:  1994-11-03       Impact factor: 49.962

10.  Positional cloning of the nude locus: genetic, physical, and transcription maps of the region and mutations in the mouse and rat.

Authors:  J A Segre; J L Nemhauser; B A Taylor; J H Nadeau; E S Lander
Journal:  Genomics       Date:  1995-08-10       Impact factor: 5.736

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  2 in total

1.  Transcriptional analysis of infiltrating T cells in kidney ischemia-reperfusion injury reveals a pathophysiological role for CCR5.

Authors:  Gang Jee Ko; Douglas Linfert; Hye Ryoun Jang; Elizabeth Higbee; Tonya Watkins; Chris Cheadle; Manchang Liu; Lorraine Racusen; Dmitry N Grigoryev; Hamid Rabb
Journal:  Am J Physiol Renal Physiol       Date:  2011-12-07

Review 2.  Immunologic research in kidney ischemia/reperfusion injury at Johns Hopkins University.

Authors:  Gang Jee Ko; Asif Zakaria; Karl L Womer; Hamid Rabb
Journal:  Immunol Res       Date:  2010-07       Impact factor: 2.829

  2 in total

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