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一种具有淋巴结增生和自身免疫病理延迟发作的新型突变无毛小鼠。

A new mutant hairless mouse with lymph node hyperplasia and late onset of autoimmune pathology.

作者信息

Massironi S M, Dagli M L, Lima M R, Alvarez J M, Kipnis T L

机构信息

Departamento de Imunologia, Universidade de São Paulo, Brasil.

出版信息

Braz J Med Biol Res. 1994 Oct;27(10):2401-5.

PMID:7640630
Abstract

Adult BALB/c male mice were injected with a single dose of ethyl nitroso urea (ENU; 250 mg/kg, i.p.) and mated to C57BL/6, DBA/2 and A/J adult females 13 weeks later. F1 males were mated with BALB/c females and F2 females were than backcrossed to the F1 parents. One BALB/c male mouse thus treated gave origin to a mutant presenting hair and skin alterations similar to those of natural hairless mutants. The new mutation is located on chromosome 14 near the Es10 locus, and probably at the same locus for the hairless mutation. Similar to the hairless mouse, this new mutant has a normal phenotype at birth and after three weeks starts to loose hair which is never replaced. Additionally, the skin becomes thickened and wrinkled. One feature that distinguishes this mutant from other hairless mice is the peculiar enlargement of its axillary and cervical lymph nodes. The new mutant develops membranoproliferative glomerulonephritis similar to the rhino mouse, one of the hairless allele mutants already described in the literature, but with a much later onset.

摘要

成年BALB/c雄性小鼠腹腔注射单剂量的乙基亚硝基脲(ENU;250毫克/千克),13周后与C57BL/6、DBA/2和A/J成年雌性小鼠交配。F1雄性小鼠与BALB/c雌性小鼠交配,然后F2雌性小鼠回交至F1亲代。一只经如此处理的BALB/c雄性小鼠产生了一个突变体,其毛发和皮肤改变与天然无毛突变体相似。这个新突变位于14号染色体上靠近Es10位点的位置,可能与无毛突变位于同一位置。与无毛小鼠相似,这个新突变体出生时表型正常,三周后开始脱毛且不再重新长毛。此外,皮肤变得增厚且起皱。该突变体与其他无毛小鼠的一个区别特征是其腋窝和颈部淋巴结异常肿大。这个新突变体发展出类似于犀牛小鼠(文献中已描述的无毛等位基因突变体之一)的膜增生性肾小球肾炎,但发病时间要晚得多。

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