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一种新型的宿主-寄生虫脂质相互作用。血吸虫溶磷脂酰丝氨酸激活Toll样受体2并影响免疫极化。

A novel host-parasite lipid cross-talk. Schistosomal lyso-phosphatidylserine activates toll-like receptor 2 and affects immune polarization.

作者信息

van der Kleij Desiree, Latz Eicke, Brouwers Jos F H M, Kruize Yvonne C M, Schmitz Marion, Kurt-Jones Evelyn A, Espevik Terje, de Jong Esther C, Kapsenberg Martien L, Golenbock Douglas T, Tielens Aloysius G M, Yazdanbakhsh Maria

机构信息

Department of Parasitology, Leiden University Medical Center, The Netherlands.

出版信息

J Biol Chem. 2002 Dec 13;277(50):48122-9. doi: 10.1074/jbc.M206941200. Epub 2002 Sep 30.

DOI:10.1074/jbc.M206941200
PMID:12359728
Abstract

Schistosome infections are characterized by prominent T cell hyporesponsiveness during the chronic stage of infection. We found that schistosome-specific phosphatidylserine (PS) activated TLR2 and affected dendritic cells such that mature dendritic cells gained the ability to induce the development of IL-10-producing regulatory T cells. Using mass spectrometry, schistosomal lysophosphatidylserine (lyso-PS) was identified as the TLR2-activating molecule. This activity appears to be a unique property of schistosomal lyso-PS, containing specific acyl chains, because neither a synthetic lyso-PS (16:0) nor PS isolated from the mammalian host activates TLR2. Taken together, these findings provide evidence for a novel host-parasite interaction that may be central to long term survival of the parasite and limited host pathology with implications beyond parasitology.

摘要

血吸虫感染的特征是在感染的慢性阶段出现显著的T细胞低反应性。我们发现,血吸虫特异性磷脂酰丝氨酸(PS)激活TLR2并影响树突状细胞,使得成熟的树突状细胞获得了诱导产生白细胞介素-10的调节性T细胞发育的能力。通过质谱分析,血吸虫溶血磷脂酰丝氨酸(lyso-PS)被鉴定为激活TLR2的分子。这种活性似乎是血吸虫lyso-PS的独特特性,其含有特定的酰基链,因为合成的lyso-PS(16:0)和从哺乳动物宿主分离的PS均不能激活TLR2。综上所述,这些发现为一种新的宿主-寄生虫相互作用提供了证据,这种相互作用可能是寄生虫长期存活和有限宿主病理的核心,其影响超出了寄生虫学领域。

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