Hydronephrosis with ureteritis developed in C57BL/6N mice carrying the congenic region derived from MRL/MpJ-type chromosome 11
Hydronephrosis with ureteritis developed in C57BL/6N mice carrying the congenic region derived from MRL/MpJ-type chromosome 11
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携带来自 MRL/MpJ 型 11 号染色体的同源区域的 C57BL/6N 小鼠出现肾积水伴输尿管炎
DOI:
10.1080/08916934.2016.1261831
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发表时间:
2017
期刊:
影响因子:
3.5
通讯作者:
Y. Kon
中科院分区:
文献类型:
--
作者:
O. Ichii;Masataka Chihara;Shin;Teppei Nakamura;Saori Otsuka;T. Horino;Y. Elewa;Y. Kon
Abstract Inbred MRL/MpJ mice show several unique phenotypes in tissue regeneration processes and the urogenital and immune systems. Clarifying the genetic and molecular bases of these phenotypes requires the analysis of their genetic susceptibility locus. Herein, hydronephrosis development was incidentally observed in MRL/MpJ-derived chromosome 11 (D11Mit21-212)-carrying C57BL/6N-based congenic mice, which developed bilateral or unilateral hydronephrosis in both males and females with 23.5% and 12.5% prevalence, respectively. Histopathologically, papillary malformations of the transitional epithelium in the pelvic-ureteric junction seemed to constrict the ureter luminal entrance. Characteristically, eosinophilic crystals were observed in the lumen of diseased ureters. These ureters were surrounded by infiltrating cells mainly composed of numerous CD3+ T-cells and B220+ B-cells. Furthermore, several Iba-1+ macrophages, Gr-1+ granulocytes, mast cells and chitinase 3-like 3/Ym1 (an important inflammatory lectin)-positive cells were detected. Eosinophils also accumulated to these lesions in diseased ureters. Some B6.MRL-(D11Mit21-D11Mit212) mice had duplicated ureters. We determined >100 single nucleotide variants between C57BL/6N- and MRL/MpJ-type chromosome 11 congenic regions, which were associated with nonsynonymous substitution, frameshift or stopgain of coding proteins. In conclusion, B6.MRL-(D11Mit21-D11Mit212) mice spontaneously developed hydronephrosis due to obstructive uropathy with inflammation. Thus, this mouse line would be useful for molecular pathological analysis of obstructive uropathy in experimental medicine.
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影响因子:
2.3
作者:
Nio, J;Fujimoto, W;Iwanaga, T
通讯作者:
Iwanaga, T
DOI:
--
发表时间:
2009
期刊:
影响因子:
--
作者:
Lee;S. -H
通讯作者:
S. -H
DOI:
--
发表时间:
2005
期刊:
Mammal. Genome 16(2)
影响因子:
--
作者:
Namiki;Y.
通讯作者:
Y.
影响因子:
19.6
作者:
Ichii, Osamu;Konno, Akihiro;Kon, Yasuhiro
通讯作者:
Kon, Yasuhiro
影响因子:
2.6
作者:
Ichii, O.;Kamikawa, A.;Kon, Y.
通讯作者:
Kon, Y.