Kinjoh K, Kyogoku M, Good R A
Department of Pathology, Tohoku University School of Medicine, Sendai, Japan.
Proc Natl Acad Sci U S A. 1993 Apr 15;90(8):3413-7. doi: 10.1073/pnas.90.8.3413.
We have established a recombinant inbred strain of mouse named spontaneous crescentic glomerulonephritis-forming mouse/Kinjoh or SCG/Kj. Mice of this strain spontaneously develop rapidly progressive glomerulonephritis. This strain of mice was derived from (BXSB/Mp x MRL/Mp-lpr/lpr)F1 hybrid mice by brother x sister mating coupled with repeated histopathologic selection for breeding of mice whose parents had the highest frequency of crescent formation in the kidneys. In this strain of mice, nephritis appears earlier and is more rapidly progressive than in any other murine model of systemic lupus erythematosus. Histopathologically, the characteristic renal lesions in the mice of this strain express a most dramatic form of crescentic glomerulonephritis. The lesions in the kidneys show only slight fine granular immune deposits along the glomerular basement membrane associated with remarkable extraglomerular proliferation and hemorrhage in Bowman's space. Although selection was not based on vasculitis, mice of this strain also exhibit a high incidence of necrotizing vasculitis. These vascular lesions involve primarily small arteries and arterioles and many organs and tissues but spare the kidneys. Thus this form of vasculitis has been found to be correlated with the crescentic form of glomerulonephritis but not with lymphoid hyperplasia of the spleen. We conclude that, in this strain of mouse, the rapidly progressive glomerulonephritis is genetically restricted and that this genetic restriction is firmly linked to that responsible for the vasculitis.
我们已经培育出一种名为自发性新月体性肾小球肾炎形成小鼠/金松或SCG/Kj的重组近交系小鼠。该品系小鼠会自发发展为快速进行性肾小球肾炎。此品系小鼠源自(BXSB/Mp×MRL/Mp-lpr/lpr)F1杂交小鼠,通过兄妹交配,并对其父母肾脏中新月体形成频率最高的小鼠进行反复组织病理学筛选以用于繁殖。在该品系小鼠中,肾炎出现得更早,且比其他任何系统性红斑狼疮小鼠模型发展得更快。组织病理学上,该品系小鼠特征性的肾脏病变表现为最显著的新月体性肾小球肾炎形式。肾脏病变仅在肾小球基底膜处显示轻微的细颗粒状免疫沉积物,伴有鲍曼间隙显著的球外增殖和出血。尽管筛选并非基于血管炎,但该品系小鼠也表现出高发性坏死性血管炎。这些血管病变主要累及小动脉和小静脉以及许多器官和组织,但不累及肾脏。因此,已发现这种血管炎形式与新月体性肾小球肾炎相关,但与脾脏的淋巴样增生无关。我们得出结论,在该品系小鼠中,快速进行性肾小球肾炎受到基因限制,且这种基因限制与导致血管炎发生的基因限制紧密相关。