Increased peripheral and local soluble FGL2 in the recovery of renal ischemia reperfusion injury in a porcine kidney auto-transplantation model.
Increased peripheral and local soluble FGL2 in the recovery of renal ischemia reperfusion injury in a porcine kidney auto-transplantation model.
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猪肾自体移植模型肾缺血再灌注损伤恢复过程中外周和局部可溶性 FGL2 的增加
DOI:
10.1186/1479-5876-12-53
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发表时间:
2014-02-23
影响因子:
7.4
通讯作者:
Zhu T
中科院分区:
文献类型:
--
作者:
Zhao Z;Yang C;Li L;Zhao T;Wang L;Rong R;Yang B;Xu M;Zhu T
BackgroundRegulatory T cells (Treg) protect kidney against ischemia reperfusion (IR) injury via suppressing innate immunity, but the mechanism has not been fully clarified. Soluble fibrinogen-like protein 2 (sFGL2), a novel effector of Treg, may affect apoptosis and inflammation. This study investigated the role of sFGL2 in renal IR injury in a porcine kidney auto-transplantation model.Materials and methodsThe left kidney was retrieved from mini pigs and infused by University of Wisconsin solution into the renal artery with the renal artery and vein clamped for 24-h cold storage. After the right nephrectomy, the left kidney was auto-transplanted into the right for 2 weeks. 3 pigs were sacrificed at day 2, 5, 7, 10 and 14 post-transplantation respectively. Collected renal tissues and daily blood samples were stored for further analyses.ResultsBoth serum creatinine and blood urea nitrogen were maximized during day 2 to 5 and followed by a gradual recovery over 2 weeks. The similar pattern were showed in histological damage, myeloperoxidase + cells and apoptosis in the kidney, as well as circulating TNF-α and IFN-γ. Serum sFGL2 presented a fluctuating increase and reached a peak at day 10. The expression of sFGL2 and its receptor FcγRIIB as well as Foxp3 and IL-10 in the kidney was notably increased from day 5 to 10.ConclusionThe increased sFGL2 together with FcγRIIB during renal recovery after IR injury suggested that sFGL2 might be a potential renoprotective mediator involved in the renal self-repairing and remodeling in this 2-week porcine auto-transplantation model.
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DOI:
10.18632/aging.100459
发表时间:
2012-05
期刊:
Aging
影响因子:
--
作者:
Favaloro B;Allocati N;Graziano V;Di Ilio C;De Laurenzi V
通讯作者:
De Laurenzi V
DOI:
10.1186/1756-9966-30-87
发表时间:
2011-09-26
期刊:
Journal of experimental & clinical cancer research : CR
影响因子:
--
作者:
Wong RS
通讯作者:
Wong RS
DOI:
10.1007/978-94-007-2869-1_7
发表时间:
2012-01-01
期刊:
ADVANCES IN MITOCHONDRIAL MEDICINE
影响因子:
--
作者:
Estaquier, Jerome;Vallette, Francois;Mignotte, Bernard
通讯作者:
Mignotte, Bernard
影响因子:
0.9
作者:
Du, C;Guan, Q;Jevnikar, AM
通讯作者:
Jevnikar, AM
影响因子:
6.2
作者:
Guan, Qiunong;Nguan, Christopher Y. C.;Du, Caigan
通讯作者:
Du, Caigan