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Monocyte Heterogeneity: Consequences for Monocyte-Derived Immune Cells.单核细胞异质性:对单核细胞衍生免疫细胞的影响。
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Classification of the medicinal plants of the genus Atractylodes using high-performance liquid chromatography with diode array and tandem mass spectrometry detection combined with multivariate statistical analysis.采用二极管阵列-串联质谱检测的高效液相色谱法结合多元统计分析对白术属药用植物进行分类
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PCSK9 is a critical regulator of the innate immune response and septic shock outcome.前蛋白转化酶枯草溶菌素9(PCSK9)是先天性免疫反应和脓毒性休克结局的关键调节因子。
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Toll-like receptor signaling pathways.Toll样受体信号通路。
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Monocytes and macrophages: developmental pathways and tissue homeostasis.单核细胞和巨噬细胞:发育途径与组织稳态
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Bioactivity-guided isolation of polyacetylenes with inhibitory activity against NO production in LPS-activated RAW264.7 macrophages from the rhizomes of Atractylodes macrocephala.从白术根茎中通过对 LPS 激活的 RAW264.7 巨噬细胞中 NO 产生有抑制活性的生物活性导向分离化合物聚乙炔。
J Ethnopharmacol. 2014 Feb 3;151(2):791-9. doi: 10.1016/j.jep.2013.10.005. Epub 2013 Dec 1.
8
T helper cells plasticity in inflammation.辅助性 T 细胞在炎症中的可塑性。
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Maintenance of peripheral naive T cells is sustained by thymus output in mice but not humans.在小鼠中,外周初始 T 细胞的维持依赖于胸腺输出,但在人类中并非如此。
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口服小柴胡汤水提取物对小鼠巨噬细胞和T细胞炎症反应的影响。

Effect of Orally Administered Koidz Water Extract on Macrophage and T Cell Inflammatory Response in Mice.

作者信息

Kwak Tae-Kyung, Jang Hyung-Seok, Lee Mi-Gi, Jung Young-Sung, Kim Dae-Ok, Kim Yoon-Bum, Kim Jong-In, Kang Hee

机构信息

Graduate School of East-West Medical Science, Kyung Hee University, Yongin 17104, Republic of Korea.

Jang Hyung-Seok Korean Medicine Clinic, Seoul 06524, Republic of Korea.

出版信息

Evid Based Complement Alternat Med. 2018 Aug 7;2018:4041873. doi: 10.1155/2018/4041873. eCollection 2018.

DOI:10.1155/2018/4041873
PMID:30174703
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6106947/
Abstract

The rhizome of Koidz (AM) is a constituent of various Qi booster compound prescriptions. We evaluated inflammatory responses in macrophages and T cells isolated from mice following oral administration of AM water extract (AME). Peritoneal exudate cells were isolated from thioglycollate-injected mice and alterations in scavenger receptors were examined. Peritoneal macrophages were stimulated with lipopolysaccharide (LPS). Serum cytokine responses to intraperitoneal LPS injection were also evaluated. Splenocytes were isolated and their composition and functional responses were measured. The content of atractylenolide I and atractylenolide III, known anti-inflammatory ingredients, in AME was 0.0338 mg/g extract and 0.565 mg/g extract, respectively. AME increased the number of SRA(+)CD11b(+) cells in response to thioglycollate. Peritoneal macrophages isolated from the AME group showed no changes in inflammatory markers such as tumor necrosis factor- (TNF-) , interleukin- (IL-) 6, inducible nitric oxide synthase, and cyclooxygenase-2 but exhibited a decrease in CD86 expression. Interestingly, AME decreased the serum levels of TNF- and IL-6 upon intraperitoneal injection of LPS. Regarding the adaptive immune system, AME increased the CD4(+) T cell population and major histocompatibility complex class II molecule expression in the spleen, and cultured splenocytes from the AME group showed increased production of IL-4 concurrent with decreased interferon- production during T cell activation. AME promoted the replenishment of peritoneal macrophages during the inflammatory response but its anti-inflammatory activity did not appear to be mediated by the modulation of macrophage activity. AME also altered the immune status of CD4 T cells, promoting the Th2 response.

摘要

小泽泻(AM)的根茎是各种补气复方制剂的组成成分。我们评估了口服AM水提取物(AME)后从小鼠分离出的巨噬细胞和T细胞中的炎症反应。从注射巯基乙酸盐的小鼠中分离出腹腔渗出细胞,并检测清道夫受体的变化。用脂多糖(LPS)刺激腹腔巨噬细胞。还评估了对腹腔注射LPS的血清细胞因子反应。分离脾细胞并测量其组成和功能反应。AME中已知的抗炎成分白术内酯I和白术内酯III的含量分别为0.0338mg/g提取物和0.565mg/g提取物。AME增加了对巯基乙酸盐反应的SRA(+)CD11b(+)细胞数量。从AME组分离出的腹腔巨噬细胞在肿瘤坏死因子-(TNF-)、白细胞介素-(IL-)6、诱导型一氧化氮合酶和环氧化酶-2等炎症标志物方面没有变化,但CD86表达降低。有趣的是,腹腔注射LPS后,AME降低了TNF-和IL-6的血清水平。关于适应性免疫系统,AME增加了脾脏中CD4(+)T细胞群体和主要组织相容性复合体II类分子的表达,并且AME组培养的脾细胞在T细胞活化期间显示IL-4产生增加,同时干扰素-产生减少。AME在炎症反应期间促进腹腔巨噬细胞的补充,但其抗炎活性似乎不是由巨噬细胞活性的调节介导的。AME还改变了CD4 T细胞的免疫状态,促进了Th2反应。