Biomedical Research Centre, Sheffield Hallam University, Sheffield, UK.
Transplant Immunology, St James's University Hospital, Leeds, UK.
Osteoarthritis Cartilage. 2015 Jul;23(7):1165-77. doi: 10.1016/j.joca.2015.02.017. Epub 2015 Mar 4.
OBJECTIVE: These studies investigated cytokine and chemokine receptor profiles in nucleus pulposus (NP) cells, and the effects of receptor stimulation on mRNA levels of extracellular matrix (ECM) components, degrading enzymes and cytokine and chemokine expression. METHOD: Immunohistochemistry (IHC) was performed to localise expression of CD4, CCR1, CXCR1 and CXCR2 in human NP tissue samples. Effects of cytokine and chemokine stimulation was performed to investigate effects related to ECM remodelling and modulation of cytokine and chemokine mRNA expression. RESULTS: IHC identified CD4, CCR1, CXCR1 and CXCR2 expression by NP cells. Differential expression profiles were observed for CD4 and CXCR2 in tissue samples from degenerate and infiltrated IVDs. In vitro stimulations of primary human NP cultures with IL-16, CCL2, CCL3, CCL7 or CXCL8 did not identify any modulatory effects on parameters associated with ECM remodelling or expression of other cytokines and chemokines. Conversely, IL-1 was seen to modulate ECM remodelling and expression of all other cytokines and chemokines investigated. CONCLUSION: This study demonstrates for the first time that NP cells express a number of cytokine and chemokine receptors and thus could respond in an autocrine or paracrine manner to cytokines and chemokines produced by NP cells, particularly during tissue degeneration. However, this study failed to demonstrate regulatory effects on ECM genes and degradative enzymes or other cytokines and chemokines for any target investigated, with the exception of IL-1. This suggests that IL-1 is a master regulator within the IVD and may exert regulatory potential over a plethora of other cytokines and chemokines.
目的:这些研究调查了核髓核(NP)细胞中的细胞因子和趋化因子受体谱,以及受体刺激对细胞外基质(ECM)成分、降解酶以及细胞因子和趋化因子表达的 mRNA 水平的影响。
方法:通过免疫组织化学(IHC)检测人 NP 组织样本中 CD4、CCR1、CXCR1 和 CXCR2 的表达。进行细胞因子和趋化因子刺激的实验,以研究与 ECM 重塑相关的效应,以及细胞因子和趋化因子 mRNA 表达的调节。
结果:IHC 鉴定了 NP 细胞中 CD4、CCR1、CXCR1 和 CXCR2 的表达。退变和浸润性 IVD 组织样本中观察到 CD4 和 CXCR2 的差异表达谱。体外刺激原代人 NP 培养物中的白细胞介素 16(IL-16)、CCL2、CCL3、CCL7 或 CXCL8 ,并未发现对与 ECM 重塑相关的参数或其他细胞因子和趋化因子表达有任何调节作用。相反,白细胞介素 1(IL-1)被发现调节 ECM 重塑和所有其他研究的细胞因子和趋化因子的表达。
结论:本研究首次证明 NP 细胞表达多种细胞因子和趋化因子受体,因此可以通过自分泌或旁分泌方式对 NP 细胞产生的细胞因子和趋化因子做出反应,尤其是在组织退变期间。然而,本研究未能证明任何目标的 ECM 基因和降解酶或其他细胞因子和趋化因子的调节作用,除了白细胞介素 1。这表明白细胞介素 1 是 IVD 中的主调节因子,可能对大量其他细胞因子和趋化因子发挥调节潜力。
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