首页> 外文期刊>American Journal of Pathology: Official Publication of the American Association of Pathologists >Surfactant protein a suppresses lung cancer progression by regulating the polarization of tumor-associated macrophages
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Surfactant protein a suppresses lung cancer progression by regulating the polarization of tumor-associated macrophages

机译:表面活性蛋白a通过调节肿瘤相关巨噬细胞的极化抑制肺癌的进展

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摘要

Surfactant protein A (SP-A) is a large multimeric protein found in the lungs. In addition to its immunoregulatory function in infectious respiratory diseases, SP-A is also used as a marker of lung adenocarcinoma. Despite the finding that SP-A expression levels in cancer cells has a relationship with patient prognosis, the function of SP-A in lung cancer progression is unknown. We investigated the role of SP-A in lung cancer progression by introducing the SP-A gene into human lung adenocarcinoma cell lines. SP-A gene transduction suppressed the progression of tumor in subcutaneous xenograft or lung metastasis mouse models. Immunohistochemical analysis showed that the number of M1 antitumor tumor-associated macrophages (TAMs) was increased and the number of M2 tumor-promoting TAMs was not changed in the tumor tissue produced by SP-A-expressing cells. In addition, natural killer (NK) cells were also increased and activated in the SP-A-expressing tumor. Moreover, SP-A did not inhibit tumor progression in mice depleted of NK cells. Taking into account that SP-A did not directly activate NK cells, these results suggest that SP-A inhibited lung cancer progression by recruiting and activating NK cells via controlling the polarization of TAMs.
机译:表面活性剂蛋白A(SP-A)是一种在肺中发现的大型多聚体蛋白。除了在感染性呼吸道疾病中具有免疫调节功能外,SP-A还被用作肺腺癌的标志物。尽管发现癌细胞中SP-A表达水平与患者预后有关,但尚不清楚SP-A在肺癌进展中的功能。我们通过将SP-A基因引入人肺腺癌细胞系来研究SP-A在肺癌进展中的作用。 SP-A基因转导抑制了皮下异种移植或肺转移小鼠模型中肿瘤的进展。免疫组织化学分析表明,在表达SP-A的细胞产生的肿瘤组织中,M1抗肿瘤肿瘤相关巨噬细胞(TAM)的数量增加,而促M2肿瘤的TAM的数量没有改变。另外,在表达SP-A的肿瘤中自然杀伤(NK)细胞也增加并被激活。此外,SP-A不会抑制NK细胞耗尽的小鼠的肿瘤进展。考虑到SP-A不会直接激活NK细胞,这些结果表明SP-A通过控制TAM的极化来募集和激活NK细胞来抑制肺癌的进展。

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