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发酵支原体MALP-2生物学作用研究进展
引用本文:梁珂莹,刘君,曾焱华,何军. 发酵支原体MALP-2生物学作用研究进展[J]. 南华大学学报(医学版), 2020, 0(5): 449-453
作者姓名:梁珂莹  刘君  曾焱华  何军
作者单位:南华大学附属南华医院检验科,湖南 衡阳 421002;南华大学附属南华医院检验科,湖南 衡阳 421002;南华大学衡阳医学院病原生物学研究所,特殊病原体防控湖南省重点实验室,湖南 衡阳 421001
摘    要:巨噬细胞活化脂肽-2(MALP-2)是发酵支原体(Mf)上极具代表性的外膜脂肽,N端为特殊的二酰化半胱氨酸残基结构。MALP-2是一把“双刃剑”,在致炎与抗炎、细胞凋亡与抗凋亡、免疫佐剂、生物协同与抑制、血管损伤和血管修复等方面发挥重要作用。因此,了解MALP-2复杂的生物学作用能为理解Mf的致病机制及其临床治疗方案提供依据,同时也为MALP-2的临床应用提供理论基础。

关 键 词:发酵支原体   巨噬细胞活化脂肽-2   生物学作用   致病机制
收稿时间:2020-05-07
修稿时间:2020-08-13

The progress of immunologic mechanisms of mycoplasma fermentans macrophage-activating lipopeptide-2
LIANG Keying,LIU Jun,ZENG Yanhu,HE Jun. The progress of immunologic mechanisms of mycoplasma fermentans macrophage-activating lipopeptide-2[J]. Journal of Nanhua University(Medical Edition), 2020, 0(5): 449-453
Authors:LIANG Keying  LIU Jun  ZENG Yanhu  HE Jun
Affiliation:Department of Clinical Laboratory, Nanhua Affiliated Hospital,University of South China, Hengyang 421002, Hunan, China;Department of Clinical Laboratory, Nanhua Affiliated Hospital,University of South China, Hengyang 421002, Hunan, China;Institute of Pathogenic Biology, Hengyang Medical College, University of South China Hunan Provincial Key Laboratory for Special Pathogens Prevention and Control, Hengyang 421001, Hunan, China
Abstract:Macrophage-activating lipopeptide-2(MALP-2) is a classical mycoplasma-derived outer membrane lipopeptide on Mycoplasma fermentans (Mf) with a special diacylated cysteine residue structure at the N-terminal. MALP-2 poses as a double-edged sword that plays an important role in inflammation and anti-inflammation, apoptosis and anti-apoptosis, immune adjuvant, biological synergy, biological inhibition, vascular injury and vascular repair, etc. Therefore, making out the complex immunologic mechanisms of MALP-2 can provide a basis for understanding the pathogenesis of Mf and its clinical treatment, which also provides a theoretical basis for the clinical application of MALP-2.
Keywords:mycoplasma fermentans   macrophage-activating lipopeptide-2   immuno- logic mechanisms   pathogenesis
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