探索碱蛋白尿中炎症和淀粉样蛋白生成事件的体外细胞模型。

IF 4.5 2区 生物学 Q2 CELL BIOLOGY Journal of Cellular Physiology Pub Date : 2024-10-01 DOI:10.1002/jcp.31449
Pierfrancesco Mastroeni, Michela Geminiani, Tommaso Olmastroni, Luisa Frusciante, Alfonso Trezza, Anna Visibelli, Annalisa Santucci
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引用次数: 0

摘要

钾离子尿症(AKU)是一种进行性系统性遗传代谢疾病,主要影响骨关节系统,其特点是软骨因chronosis而退化,最终导致早期骨关节炎(OA)。然而,在人类软骨细胞中研究 AKU 病理学对了解这种疾病至关重要,但由于可用性有限和供体的可变性,研究工作遇到了挑战。为了克服这一障碍,我们利用同庚二酸(HGA)建立了一个体外模型来模拟 AKU 条件。该模型采用了永生化的 C20/A4 人类软骨细胞,是研究 AKU 发病机制的可靠平台。值得注意的是,该模型显示了经 HGA 处理的细胞中chronotic 色素的积累,这与之前的研究结果一致。此外,对暴露于 HGA 过程中的炎症过程的研究发现,活性氧和脂质过氧化水平的升高表明存在明显的氧化应激。此外,该模型还显示了 HGA 诱导的炎症反应,表现为一氧化氮的产生增加、诱导型一氧化氮合酶和环氧合酶-2 的过度表达。这些发现强调了该模型在研究与 AKU 相关的炎症方面的实用性。此外,对血清淀粉样蛋白 A 和血清淀粉样蛋白 P 的分析表明,两者之间可能存在相互作用,这也证实了淀粉样纤维形成的证据。刚果红染色法进一步支持了这一假设,该染色法显示只有 HGA 处理过的细胞才会形成纤维。总之,C20/A4 细胞模型为了解 AKU 发病机制提供了宝贵的见解,强调了其促进药物开发和治疗干预的潜力。
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An in vitro cell model for exploring inflammatory and amyloidogenic events in alkaptonuria.

Alkaptonuria (AKU) is a progressive systemic inherited metabolic disorder primarily affecting the osteoarticular system, characterized by the degeneration of cartilage induced by ochronosis, ultimately leading to early osteoarthritis (OA). However, investigating AKU pathology in human chondrocytes, which is crucial for understanding the disease, encounters challenges due to limited availability and donor variability. To overcome this obstacle, an in vitro model has been established using homogentisic acid (HGA) to simulate AKU conditions. This model employed immortalized C20/A4 human chondrocytes and serves as a dependable platform for studying AKU pathogenesis. Significantly, the model demonstrates the accumulation of ochronotic pigment in HGA-treated cells, consistent with findings from previous studies. Furthermore, investigations into inflammatory processes during HGA exposure revealed notable oxidative stress, as indicated by elevated levels of reactive oxygen species and lipid peroxidation. Additionally, the model demonstrated HGA-induced inflammatory responses, evidenced by increased production of nitric oxide, overexpression of inducible nitric oxide synthase, and cyclooxygenase-2. These findings underscore the model's utility in studying inflammation associated with AKU. Moreover, analysis of serum amyloid A and serum amyloid P proteins revealed a potential interaction, corroborating evidence of amyloid fibril formation. This hypothesis was further supported by Congo red staining, which showed fibril formation exclusively in HGA-treated cells. Overall, the C20/A4 cell model provided valuable insights into AKU pathogenesis, emphasizing its potential for facilitating drug development and therapeutic interventions.

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来源期刊
CiteScore
14.70
自引率
0.00%
发文量
256
审稿时长
1 months
期刊介绍: The Journal of Cellular Physiology publishes reports of high biological significance in areas of eukaryotic cell biology and physiology, focusing on those articles that adopt a molecular mechanistic approach to investigate cell structure and function. There is appreciation for the application of cellular, biochemical, molecular and in vivo genetic approaches, as well as the power of genomics, proteomics, bioinformatics and systems biology. In particular, the Journal encourages submission of high-interest papers investigating the genetic and epigenetic regulation of proliferation and phenotype as well as cell fate and lineage commitment by growth factors, cytokines and their cognate receptors and signal transduction pathways that influence the expression, integration and activities of these physiological mediators. Similarly, the Journal encourages submission of manuscripts exploring the regulation of growth and differentiation by cell adhesion molecules in addition to the interplay between these processes and those induced by growth factors and cytokines. Studies on the genes and processes that regulate cell cycle progression and phase transition in eukaryotic cells, and the mechanisms that determine whether cells enter quiescence, proliferate or undergo apoptosis are also welcomed. Submission of papers that address contributions of the extracellular matrix to cellular phenotypes and physiological control as well as regulatory mechanisms governing fertilization, embryogenesis, gametogenesis, cell fate, lineage commitment, differentiation, development and dynamic parameters of cell motility are encouraged. Finally, the investigation of stem cells and changes that differentiate cancer cells from normal cells including studies on the properties and functions of oncogenes and tumor suppressor genes will remain as one of the major interests of the Journal.
期刊最新文献
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