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氧化应激诱导鸡胚肢芽来源软骨细胞中的多聚(ADP-核糖)化作用

Oxidative stress-induced poly(ADP-ribosyl)ation in chick limb bud-derived chondrocytes.

作者信息

Zákány Róza, Bakondi Edina, Juhász Tamás, Matta Csaba, Szíjgyártó Zsolt, Erdélyi Katalin, Szabó Eva, Módis László, Virág László, Gergely Pál

机构信息

Department of Anatomy, Histology and Embryology, Research Center for Molecular Medicine, Medical and Health Science Center, University of Debrecen, Debrecen, Hungary.

出版信息

Int J Mol Med. 2007 Apr;19(4):597-605.

Abstract

Oxidative stress has been implicated in the pathogenesis of various diseases affecting chondrogenesis or the function of articular cartilage. DNA damage caused by oxidative stress may trigger the activation of the nuclear enzyme, poly(ADP-ribose) polymerase-1 (PARP-1) which may contribute to tissue injury. We aimed at investigating the effects of peroxynitrite (100-600 microM) and hydrogen peroxide (0.1-4 mM) on PARP activation and extracellular matrix production of high density micromass cultures (HDC) prepared from chick limb bud mesenchymal cells. We found that both oxidative species strongly inhibited matrix formation of HDCs treated on day 2 but not on day 5. The PARP inhibitor 3-aminobenzamide (3-AB) stimulated matrix production in non-stressed cells and prevented suppressed matrix production in oxidatively stressed cells. Both hydrogen peroxide and peroxynitrite induced PARP activation and poly(ADP-ribose) accumulation. Decreased proliferation, viability and NAD+ content were not or only slightly improved by 3-AB, indicating that 3-AB directly affects matrix formation. In conclusion, oxidative stress stimulates poly(ADP-ribose) metabolism and inhibits extracellular matrix production of HDCs in a PARP-dependent manner. Our findings may have implications for potential therapeutic approaches aimed at restoring the matrix production capacity of chondrogenic cells.

摘要

氧化应激与影响软骨形成或关节软骨功能的各种疾病的发病机制有关。氧化应激引起的DNA损伤可能会触发核酶聚(ADP - 核糖)聚合酶 - 1(PARP - 1)的激活,这可能导致组织损伤。我们旨在研究过氧亚硝酸盐(100 - 600 microM)和过氧化氢(0.1 - 4 mM)对由鸡胚肢芽间充质细胞制备的高密度微团培养物(HDC)中PARP激活和细胞外基质产生的影响。我们发现,这两种氧化物质均强烈抑制在第2天处理的HDC的基质形成,但对第5天处理的HDC无此作用。PARP抑制剂3 - 氨基苯甲酰胺(3 - AB)刺激未受应激细胞的基质产生,并防止氧化应激细胞中被抑制的基质产生。过氧化氢和过氧亚硝酸盐均诱导PARP激活和聚(ADP - 核糖)积累。3 - AB对细胞增殖、活力和NAD + 含量的降低没有或仅有轻微改善,表明3 - AB直接影响基质形成。总之,氧化应激以PARP依赖的方式刺激聚(ADP - 核糖)代谢并抑制HDC的细胞外基质产生。我们的发现可能对旨在恢复软骨形成细胞基质产生能力的潜在治疗方法具有启示意义。

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