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炎症诱导的穿过皮肤和传入淋巴管迁移的细胞的表型和细胞因子谱变化。

Inflammation-induced changes in the phenotype and cytokine profile of cells migrating through skin and afferent lymph.

作者信息

Egan P J, Kimpton W, Seow H F, Bowles V M, Brandon M R, Nash A D

机构信息

Center for Animal Biotechnology, University of Melbourne, Parkville, Victoria, Australia.

出版信息

Immunology. 1996 Dec;89(4):539-46. doi: 10.1046/j.1365-2567.1996.d01-776.x.

Abstract

In the present study, we have localized cytokine-secreting cells within an ectoparasite-induced inflammatory lesion and monitored the phenotype and cytokine profile of cells migrating from the inflammatory lesion to the local draining lymph node via the afferent lymphatics. Interleukin (IL)-8-producing cells were first detected in skin within 6 hr of infection, with increased numbers observed at 24 and 48 hr post infection. While these cells were concentrated within the neutrophil influx, adjacent to disrupted epidermis; they were also found scattered throughout the surrounding dermis in areas where significant cellular infiltration was not apparent. IL-1 alpha- and IL-1 beta-producing cells could not be detected until 24 hr after infection and were restricted to areas of intense neutrophil accumulation. Concurrent with the onset of inflammation was a threefold increase in the total number of cells migrating through the draining afferent lymph. This increase in cellularity was due primarily to increased migration of CD4 and gamma delta T cells. Cytokine mRNA synthesis by migrating afferent lymph cells was examined by reverse transcription-polymerase chain reaction (RT-PCR) analysis of RNA extracted prior to, and at regular intervals during the course of the inflammatory response. IL-1 beta and IL-8, but not IL-1 alpha or IL-6 mRNA, was detected in migrating afferent lymph cells. Tumour necrosis factor (TNF)-alpha-specific mRNA was present in migrating afferent lymph cells at all time points both prior to, and following infection. Soluble IL-8 protein, but not IL-1 alpha, IL-1 beta or TNF-alpha protein, could be detected in lymph, with the amount of IL-8 detected increasing as the infection progressed. mRNA coding for cytokines associated with T-cell activation, such as IL-2, IL-4 or interferon (IFN)-gamma, was also detected in migrating cells, although the cytokine profiles of different experimental animals were extremely variable.

摘要

在本研究中,我们已将细胞因子分泌细胞定位在体外寄生虫诱导的炎性病变内,并监测了从炎性病变经输入淋巴管迁移至局部引流淋巴结的细胞的表型和细胞因子谱。感染后6小时内首次在皮肤中检测到产生白细胞介素(IL)-8的细胞,感染后24小时和48小时观察到数量增加。虽然这些细胞集中在中性粒细胞浸润部位,紧邻破损的表皮;但在周围真皮中细胞明显浸润不明显的区域也发现它们散在分布。直到感染后24小时才能检测到产生IL-1α和IL-1β的细胞,且它们局限于中性粒细胞大量聚集的区域。与炎症开始同时,通过引流输入淋巴管迁移的细胞总数增加了两倍。细胞数量的增加主要是由于CD4和γδT细胞迁移增加。通过对炎症反应过程中定期提取的RNA进行逆转录-聚合酶链反应(RT-PCR)分析,检测迁移的输入淋巴细胞的细胞因子mRNA合成。在迁移的输入淋巴细胞中检测到IL-1β和IL-8的mRNA,但未检测到IL-1α或IL-6的mRNA。在感染前和感染后的所有时间点,迁移的输入淋巴细胞中均存在肿瘤坏死因子(TNF)-α特异性mRNA。在淋巴中可检测到可溶性IL-8蛋白,但未检测到IL-1α、IL-1β或TNF-α蛋白。随着感染进展,检测到的IL-8量增加。在迁移细胞中也检测到编码与T细胞活化相关的细胞因子的mRNA,如IL-2、IL-4或干扰素(IFN)-γ,尽管不同实验动物的细胞因子谱变化极大。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0258/1456578/a51b5f0bb6c7/immunology00030-0069-a.jpg

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