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脑膜炎奈瑟菌脂多糖对诱导单核细胞和微粒体相关组织因子活性至关重要,但对组织因子表达无作用。

LPS from Neisseria meningitidis is crucial for inducing monocyte- and microparticle-associated tissue factor activity but not for tissue factor expression.

机构信息

Blood Cell Research Unit, Section for Research, Department of Medical Biochemistry, Oslo University Hospital, Ullevål, Norway.

出版信息

Innate Immun. 2012 Aug;18(4):580-91. doi: 10.1177/1753425911428230. Epub 2011 Dec 16.

Abstract

Neisseria meningitidis causes sepsis with coagulopathy. The present study evaluated the tissue factor (TF)-inducing capacity of bacterial LPS in different presentation forms, i.e. membrane-bound LPS versus purified LPS, and of non-LPS components of N. meningitidis. By using a wild-type N. meningitidis, a mutant N. meningitidis lacking LPS (LPS-deficient N. meningitidis), purified LPS from N. meningitidis and Escherichia coli, we measured TF-expression and TF-activity on human monocytes and microparticles (MPs). The effect of TF-modulators, such as phosphatidylserine (PS), tissue factor pathway inhibitor (TFPI) and recombinant IL-10 (rhIL-10) was investigated. In plasmas from meningococcal patients, fibrinopeptide A (FPA), LPS and IL-10 were quantified. Monocytes and MPs exposed to purified LPS or wild-type N. meningitidis had much higher TF-activity than monocytes and MPs exposed to LPS-deficient N. meningitidis (clot formation assay). Incubation with wild-type N. meningitidis, but also LPS-deficient N. meningitidis, resulted in TF-expression on monocytes (flow cytometry, qRT-PCR). Increased cellular TF-activity is associated with coincident surface-exposure of PS and the number of monocytes positive for both PS and TF was significantly higher for monocytes exposed to wild-type N. meningitidis (7.6%) compared with monocytes exposed to LPS-deficient N. meningitidis (1.8%). Treatment with rhIL-10 reduced monocyte- and MP-associated TF-activity, the number of monocytes positive for both TF and PS, and microvesiculation. Patients with meningococcal septicemia had significantly higher levels of LPS, FPA and IL-10 than patients with distinct meningitis. Our results indicate that LPS from N. meningitidis is crucial for inducing TF-activity, but not for monocyte- and MP-associated TF-expression. TF-activity seems to require coincident expression of TF and PS on monocytes, and LPS induces such double-positive monocytes.

摘要

脑膜炎奈瑟菌引起伴有凝血功能障碍的败血症。本研究评估了不同形式的细菌脂多糖(LPS),即膜结合 LPS 与纯化 LPS,以及脑膜炎奈瑟菌非 LPS 成分的组织因子(TF)诱导能力。我们使用野生型脑膜炎奈瑟菌、缺乏 LPS(LPS 缺陷型脑膜炎奈瑟菌)的脑膜炎奈瑟菌突变体、脑膜炎奈瑟菌和大肠杆菌的纯化 LPS,测量了人类单核细胞和微颗粒(MPs)上的 TF 表达和 TF 活性。研究了 TF 调节剂,如磷脂酰丝氨酸(PS)、组织因子途径抑制剂(TFPI)和重组白细胞介素-10(rhIL-10)的作用。在脑膜炎奈瑟菌患者的血浆中,定量了纤维蛋白肽 A(FPA)、LPS 和白细胞介素-10。与暴露于 LPS 缺陷型脑膜炎奈瑟菌(凝块形成测定)的单核细胞和 MPs 相比,暴露于纯化 LPS 或野生型脑膜炎奈瑟菌的单核细胞和 MPs 具有更高的 TF 活性。与 LPS 缺陷型脑膜炎奈瑟菌孵育也导致单核细胞上的 TF 表达(流式细胞术,qRT-PCR)。细胞 TF 活性的增加与 PS 的同时表面暴露有关,并且与暴露于野生型脑膜炎奈瑟菌的单核细胞(7.6%)相比,同时表达 PS 和 TF 的单核细胞的数量明显更高,而暴露于 LPS 缺陷型脑膜炎奈瑟菌的单核细胞为 1.8%。rhIL-10 治疗降低了单核细胞和 MPs 相关的 TF 活性、同时表达 TF 和 PS 的单核细胞数量以及微泡形成。患有脑膜炎奈瑟菌败血症的患者的 LPS、FPA 和白细胞介素-10 水平明显高于患有明确脑膜炎的患者。我们的结果表明,脑膜炎奈瑟菌的 LPS 对于诱导 TF 活性至关重要,但对于单核细胞和 MPs 相关的 TF 表达则不是必需的。TF 活性似乎需要单核细胞上 TF 和 PS 的同时表达,而 LPS 诱导这种双阳性单核细胞。

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