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免疫干扰素可抑制培养的人关节软骨细胞和肋软骨细胞中前胶原mRNA水平及II型胶原的合成。

Immune interferon suppresses levels of procollagen mRNA and type II collagen synthesis in cultured human articular and costal chondrocytes.

作者信息

Goldring M B, Sandell L J, Stephenson M L, Krane S M

出版信息

J Biol Chem. 1986 Jul 5;261(19):9049-55.

PMID:3087985
Abstract

Cultured human articular and costal chondrocytes were used as a model system to examine the effects of recombinant gamma-interferon (IFN-gamma) on synthesis of procollagens, the steady state levels of types I and II procollagen mRNAs, and the expression of major histocompatibility complex class II (Ia-like) antigens on the cell surface. Adult articular chondrocytes synthesized mainly type II collagen during weeks 1-3 of primary culture, whereas types I and III collagens were also produced after longer incubation and predominated after the first subculture. Juvenile costal chondrocytes synthesized no detectable alpha 2(I) collagen chains until after week 1 of primary culture; type II collagen was the predominant species even after weeks of culture. The relative amounts of types I and II collagens synthesized were reflected in the levels of alpha 1(I), alpha 2(I), and alpha 1(II) procollagen mRNAs. In articular chondrocytes, the levels of alpha 1(I) procollagen mRNA were disproportionately low (alpha 1(I)/alpha 2(I) less than 1.0) compared with costal chondrocytes (alpha 1 (I)/alpha 2(I) approximately 2). Recombinant IFN-gamma (0.1-100 units/ml) inhibited synthesis of type II as well as types I and III collagens associated with suppression of the levels of alpha 1(I), alpha 2(I), and alpha 1(II) procollagen mRNAs. IFN-gamma suppressed the levels of alpha 1(I) and alpha 1(II) procollagen mRNAs to a greater extent than alpha 2(I) procollagen mRNA in articular but not in costal chondrocytes. Human leukocyte interferon (IFN-alpha) at 1000 units/ml suppressed collagen synthesis and procollagen mRNA levels to a similar extent as IFN-gamma at 1.0 unit/ml. In addition, IFN-gamma but not IFN-alpha induced the expression of HLA-DR antigens on intact cells. The lymphokine IFN-gamma could, therefore, have a role in suppressing cartilage matrix synthesis in vivo under conditions in which the chondrocytes are in proximity to T lymphocytes and their products.

摘要

培养的人关节软骨细胞和肋软骨细胞被用作模型系统,以研究重组γ干扰素(IFN-γ)对前胶原合成、I型和II型前胶原mRNA稳态水平以及细胞表面主要组织相容性复合体II类(Ia样)抗原表达的影响。成年关节软骨细胞在原代培养的第1至3周主要合成II型胶原,而I型和III型胶原在较长时间培养后也会产生,并在首次传代培养后占主导地位。幼年肋软骨细胞在原代培养第1周后才检测到α2(I)胶原链;即使培养数周后,II型胶原仍是主要类型。I型和II型胶原合成的相对量反映在前胶原mRNA的α1(I)、α2(I)和α1(II)水平上。在关节软骨细胞中,与肋软骨细胞(α1(I)/α2(I)约为2)相比,α1(I)前胶原mRNA水平低得不成比例(α1(I)/α2(I)小于1.0)。重组IFN-γ(0.1 - 100单位/毫升)抑制II型以及与I型和III型胶原合成相关的α1(I)、α2(I)和α1(II)前胶原mRNA水平的抑制。在关节软骨细胞而非肋软骨细胞中,IFN-γ对α1(I)和α1(II)前胶原mRNA水平的抑制程度大于α2(I)前胶原mRNA。1000单位/毫升的人白细胞干扰素(IFN-α)对胶原合成和前胶原mRNA水平的抑制程度与1.0单位/毫升的IFN-γ相似。此外,IFN-γ而非IFN-α诱导完整细胞上HLA-DR抗原的表达。因此,在软骨细胞接近T淋巴细胞及其产物的情况下,淋巴因子IFN-γ可能在体内抑制软骨基质合成中起作用。

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