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具有不同结构的硫酸软骨素对软骨细胞和巨噬细胞的活性是否不同?

Do chondroitin sulfates with different structures have different activities on chondrocytes and macrophages?

作者信息

da Cunha André L, Aguiar Jair A K, Correa da Silva Flavio S, Michelacci Yara M

机构信息

Disciplina de Biologia Molecular, Departamento de Bioquímica, Escola Paulista de Medicina, UNIFESP, São Paulo, SP, Brazil.

Disciplina de Biologia Molecular, Departamento de Bioquímica, Escola Paulista de Medicina, UNIFESP, São Paulo, SP, Brazil; Departamento de Bioquímica, Instituto de Ciências Biológicas, UFJF, Juiz de Fora, MG, Brazil.

出版信息

Int J Biol Macromol. 2017 Oct;103:1019-1031. doi: 10.1016/j.ijbiomac.2017.05.123. Epub 2017 May 20.

Abstract

The aim of the present study was to investigate the activities of natural chondroitin sulfates (CS) with different structures on cultured chondrocytes and macrophages. CS were isolated from cartilages of bovine trachea (BT), porcine trachea (PT), chicken sternum (Ch) and skate (Sk). The preparations were 90-98% pure, with ∼1% proteins, nucleic acids and keratan sulfate contaminants. Structural analysis of these CS and of commercial chondroitin 4- and 6-sulfate (C4S, C6S) have shown that most of their disaccharides are monosulfated, with varying proportions of 4- and 6-sulfation, and 2-7% non-sulfated disaccharides. Sk-CS and C6S contained detectable amounts of disulfated disaccharides. All the CS were polydisperse, with modal molecular weights of 26-135kDa. These CS had anti-inflammatory activities on both chondrocytes and macrophages, but with different efficiencies. On horse and human chondrocytes, they reduced the IL-1β-induced liberation of NO and PGE, and on RAW 264.7 immortalized macrophage-like cell line, C4S, C6S, Ch and Sk-CS decreased the LPS-induced liberation of TNF-α, but did not affect IL-6. In contrast, on bone marrow derived macrophages, C4S, C6S, BT and PT-CS reduced the LPS-induced liberation of TNF-α, IL-6, IL-1β and NO, indicating that the RAW response to CS was different from that of primary macrophages.

摘要

本研究的目的是调查不同结构的天然硫酸软骨素(CS)对培养的软骨细胞和巨噬细胞的活性。CS从牛气管(BT)、猪气管(PT)、鸡胸骨(Ch)和鳐鱼(Sk)的软骨中分离得到。这些制剂的纯度为90 - 98%,含有约1%的蛋白质、核酸和硫酸角质素污染物。对这些CS以及市售的硫酸软骨素4-和6-硫酸盐(C4S、C6S)的结构分析表明,它们的大多数二糖是单硫酸化的,4-和6-硫酸化的比例各不相同,还有2 - 7%的非硫酸化二糖。Sk-CS和C6S含有可检测量的双硫酸化二糖。所有的CS都是多分散的,其模态分子量为26 - 135kDa。这些CS对软骨细胞和巨噬细胞都有抗炎活性,但效率不同。在马和人软骨细胞上,它们减少了IL-1β诱导的NO和PGE的释放,在RAW 264.7永生化巨噬细胞样细胞系上,C4S、C6S、Ch和Sk-CS降低了LPS诱导的TNF-α的释放,但不影响IL-6。相比之下,在骨髓来源的巨噬细胞上,C4S、C6S、BT和PT-CS降低了LPS诱导的TNF-α、IL-6、IL-1β和NO的释放,表明RAW对CS的反应与原代巨噬细胞不同。

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