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补体调节蛋白在大鼠系膜增生性肾小球肾炎中的作用

The role of a complement regulatory protein in rat mesangial glomerulonephritis.

作者信息

Nishikage H, Baranyi L, Okada H, Okada N, Isobe K, Nomura A, Yoshida F, Matsuo S

机构信息

Third Department of Internal Medicine, Nagoya University School of Medicine, Japan.

出版信息

J Am Soc Nephrol. 1995 Aug;6(2):234-41. doi: 10.1681/ASN.V62234.

Abstract

The host cells are protected from the indiscriminate attack of homologous complement by the membrane-associated complement regulatory proteins. A mouse monoclonal antibody (mAb) 512 (immunoglobulin G1 subclass) has recently been described that recognizes and inhibits the function of a rat complement regulatory protein, a rat homologue of mouse Crry/p65. The aim of this work is to assess the role of a complement regulatory protein (512Ag) recognized by mAb 512 in the complement-dependent glomerular injury induced by mAb OX7 against rat Thy-1.1. For the induction of mesangial injury, the left kidney of a rat was perfused with a combination of OX7 and 512 and the perfusate was discarded from the renal vein (Group I). After the renal artery and vein were restored, the left kidney was connected to the systemic circulation. Rats were euthanized 3 h, 2 days, and 14 days later. Rats perfused either with OX7 (Group II) or with 512 (Group III) or with vehicle only (Group IV) were used as controls. At 3 h, rats of Group I showed more prominent cellular infiltration and mesangial lysis and more C3 deposition in the glomeruli than rats of Group II. Rats of Groups III and IV showed no significant changes. At Day 2, there was still significant mesangial lysis and leukocyte infiltration in Group I rats, whereas rats in other groups showed an almost normal appearance. Glomerular injury in Group I rats returned to normal by Day 14.

摘要

膜相关补体调节蛋白可保护宿主细胞免受同源补体的无差别攻击。最近报道了一种小鼠单克隆抗体(mAb)512(免疫球蛋白G1亚类),它能识别并抑制大鼠补体调节蛋白(小鼠Crry/p65的大鼠同源物)的功能。本研究的目的是评估单克隆抗体512识别的补体调节蛋白(512Ag)在单克隆抗体OX7诱导的针对大鼠Thy-1.1的补体依赖性肾小球损伤中的作用。为诱导系膜损伤,用OX7和512的混合物灌注大鼠的左肾,并将灌注液从肾静脉排出(第一组)。恢复肾动脉和静脉后,将左肾连接到体循环。3小时、2天和14天后对大鼠实施安乐死。仅用OX7灌注的大鼠(第二组)、仅用512灌注的大鼠(第三组)或仅用赋形剂灌注的大鼠(第四组)用作对照。3小时时,第一组大鼠的细胞浸润和系膜溶解比第二组大鼠更明显,肾小球中的C3沉积也更多。第三组和第四组大鼠无明显变化。在第2天,第一组大鼠仍有明显的系膜溶解和白细胞浸润,而其他组大鼠外观几乎正常。到第14天,第一组大鼠的肾小球损伤恢复正常。

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