UMR 7365 CNRS-UL IMoPA, Vandoeuvre-lès-Nancy, France.
UMR 7365 CNRS-UL IMoPA, Vandoeuvre-lès-Nancy, France; Proteomics core facility of UMS 2008 UL-CNRS-INSERM IBSLor, Vandoeuvre-lès-Nancy, France.
J Proteomics. 2020 May 15;219:103718. doi: 10.1016/j.jprot.2020.103718. Epub 2020 Feb 22.
Fibrillar collagens and proteoglycans (PGs) are quantitatively the major constituents of extracellular matrices (ECM). They carry numerous crucial post-translational modifications (PTMs) that tune the resulting biomechanical properties of the corresponding tissues. The mechanisms determining these PTMs remain largely unknown, notably because available established cell lines do not recapitulate much of the complexity of the machineries involved. ATDC5 cells are a model of chondrogenesis widely used for decades, but it remains described mostly at histological and transcriptional levels. Here, we asked to what extent this model recapitulates the events of ECM synthesis and processing occurring in cartilage. Insulin-stimulated ATDC5 cells exhibit up- or down-regulation of more than one-hundred proteins, including a number of known participants in chondrogenesis and major markers thereof. However, they also lack several ECM components considered of significant, yet more subtle, function in cartilage. Still, they assemble the large PG aggrecan and type II collagen, both carrying most of their in vivo PTMs, into an ECM. Remarkably, collagen crosslinking is fully lysyl oxidase (LOX)-dependent. The ATDC5 model recapitulates critical aspects of the cartilage ECM-processing machinery and should be useful to decipher the mechanisms involved. Proteomics data are available via ProteomeXchange with identifier PXD014121. SIGNIFICANCE: The present work provides the first proteome characterization of the ATDC5 chondrogenesis model, which has been used for decades in the field of cartilage biology. The results demonstrate the up- and down-regulation of more than one hundred proteins. Overall, specific drawbacks of the model are pointed out, that will be important to take into consideration for future studies. However, major cartilage components are massively assembled into an extracellular matrix and carry most of their post-translational modifications occurring in cartilage tissue. Unlike other available established cell lines, the ATDC5 model recapitulates major aspects of cartilage biosynthesis and should be useful in investigating the mechanisms that regulate collagen maturation events.
纤维胶原和蛋白聚糖(PGs)是细胞外基质(ECM)的主要成分,在数量上占优势。它们具有许多关键的翻译后修饰(PTMs),这些修饰可以调节相应组织的生物力学特性。决定这些 PTM 的机制在很大程度上仍然未知,特别是因为现有的已建立的细胞系不能再现所涉及的复杂机制的大部分内容。ATDC5 细胞是软骨发生的模型,已被广泛使用了几十年,但它仍然主要在组织学和转录水平上被描述。在这里,我们询问了这种模型在多大程度上再现了软骨中 ECM 合成和加工发生的事件。胰岛素刺激的 ATDC5 细胞表现出超过一百种蛋白质的上调或下调,其中包括一些已知的参与软骨发生的参与者和主要标志物。然而,它们也缺乏几种被认为在软骨中有重要但更微妙作用的 ECM 成分。尽管如此,它们还是将大量的 PG 聚集蛋白和 II 型胶原组装到 ECM 中,这两种胶原都带有其大部分体内 PTM。值得注意的是,胶原交联完全依赖赖氨酰氧化酶(LOX)。ATDC5 模型再现了软骨 ECM 加工机制的关键方面,应该有助于破译相关机制。蛋白质组学数据可通过 ProteomeXchange 以标识符 PXD014121 获得。意义:本工作首次对 ATDC5 软骨发生模型进行了蛋白质组学特征描述,该模型在软骨生物学领域已使用了几十年。结果表明,超过一百种蛋白质被上调或下调。总的来说,指出了模型的具体缺点,这对于未来的研究将是重要的考虑因素。然而,主要的软骨成分被大量组装到细胞外基质中,并带有它们在软骨组织中发生的大多数翻译后修饰。与其他现有的已建立的细胞系不同,ATDC5 模型再现了软骨生物合成的主要方面,应该有助于研究调节胶原成熟事件的机制。