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Novel Lymphotoxin Alpha (LTα) Knockout Mice with Unperturbed Tumor Necrosis Factor Expression: Reassessing LTα Biological Functions

机译:具有稳定的肿瘤坏死因子表达的新型Lymphotoxin Alpha(LTα)基因敲除小鼠:重新评估LTα生物学功能。

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摘要

Lymphotoxin alpha (LTα) can exist in soluble form and exert tumor necrosis factor (TNF)-like activity through TNF receptors. Based on the phenotypes of knockout (KO) mice, the physiological functions of LTα and TNF are considered partly redundant, in particular, in supporting the microarchitecture of the spleen and in host defense. We exploited Cre-LoxP technology to generate a novel neomycin resistance gene (neo) cassette-free LTα-deficient mouse strain (neo-free LTα KO [LTαΔ/Δ]). Unlike the “conventional” LTα−/− mice, new LTαΔ/Δ animals were capable of producing normal levels of systemic TNF upon lipopolysaccharide (LPS) challenge and were susceptible to LPS/d-galactosamine (D-GalN) toxicity. Activated neutrophils, monocytes, and macrophages from LTαΔ/Δ mice expressed TNF normally at both the mRNA and protein levels as opposed to conventional LTα KO mice, which showed substantial decreases in TNF. Additionally, the spleens of the neo-free LTα KO mice displayed several features resembling those of LTβ KO mice rather than conventional LTα KO animals. The phenotype of the new LTαΔ/Δ mice indicates that LTα plays a smaller role in lymphoid organ maintenance than previously thought and has no direct role in the regulation of TNF expression.
机译:淋巴毒素α(LTα)可以可溶形式存在,并通过TNF受体发挥类似肿瘤坏死因子(TNF)的活性。基于基因敲除(KO)小鼠的表型,LTα和TNF的生理功能被认为部分冗余,特别是在支持脾脏的微结构和宿主防御方面。我们利用Cre-LoxP技术生成了一种新的无新霉素抗性基因(neo)的无盒LTα缺陷小鼠品系(无新的LTαKO [LTαΔ/Δ])。与“常规”LTα-/-小鼠不同,新的LTαΔ/Δ动物能够通过脂多糖(LPS)攻击产生正常水平的全身性TNF,并且容易感染LPS / d-半乳糖胺(D-GalN)毒性。与传统的LTαKO小鼠相反,LTαΔ/Δ小鼠的活化的嗜中性粒细胞,单核细胞和巨噬细胞在mRNA和蛋白质水平上均正常表达TNF,而LTαKO小鼠表现出TNF的实质性降低。另外,新无LTαKO小鼠的脾脏表现出类似于LTβKO小鼠的脾脏,而不是传统的LTαKO动物的脾脏。新的LTαΔ/Δ小鼠的表型表明,LTα在淋巴器官维持中的作用比以前认为的要小,并且在TNF表达的调节中没有直接作用。

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