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多发性硬化症中储存式钙内流相关调节因子(SARAF)的渐进性升高及钙信号通路失调

Progressive Elevation of Store-Operated Calcium Entry-Associated Regulatory Factor (SARAF) and Calcium Pathway Dysregulation in Multiple Sclerosis.

作者信息

Taha Safa, Aljishi Muna, Sultan Ameera, Al-Nashmi Moudi E, Bakhiet Moiz, Spicuglia Salvatore, Belhocine Mohamed

机构信息

Princess Al Jawhara Center for Molecular Medicine, Genetics and Inherited Diseases, Department of Molecular Medicine, College of Medicine and Health Sciences, Arabian Gulf University, Manama P.O. Box 26671, Bahrain.

Aix-Marseille University, INSERM, TAGC, UMR1090, Equipe Labélisée Ligue Contre le Cancer, 13288 Marseille, France.

出版信息

Int J Mol Sci. 2025 May 9;26(10):4520. doi: 10.3390/ijms26104520.

Abstract

Multiple Sclerosis (MS) is a chronic autoimmune disorder characterized by demyelination and neuronal damage in the central nervous system. Dysregulation of calcium homeostasis, particularly through the Store-Operated Calcium Entry-Associated Regulatory Factor (SARAF), has been implicated in MS pathogenesis. This study investigated SARAF, STIM1, and Orai1 expression patterns and their relationship to calcium homeostasis in 45 Bahraini MS patients and 45 matched healthy controls using ELISA and real-time PCR analyses. MS patients showed significantly elevated serum SARAF levels in both early (192.26 ± 47.00 pg/mL) and late MS stages (341.47 ± 96.19 pg/mL) compared to controls (129.82 ± 30.82 pg/mL; < 0.001. SARAF expressions were markedly increased in MS patients (3.829 ± 0.04422 vs. 1 ± 0; < 0.0001), while STIM1 (0.4324 ± 0.01471) and ORAI1 (0.2963 ± 0.02156) expressions were significantly reduced compared to the controls ( < 0.0001). Intracellular calcium levels were notably elevated in both early and late MS stages. These findings suggest that the progressive elevation of SARAF, coupled with altered STIM1 and ORAI1 expression, may serve as potential biomarkers for MS progression and represent promising therapeutic targets.

摘要

多发性硬化症(MS)是一种慢性自身免疫性疾病,其特征是中枢神经系统脱髓鞘和神经元损伤。钙稳态失调,特别是通过储存-操纵性钙内流相关调节因子(SARAF),与MS发病机制有关。本研究使用酶联免疫吸附测定(ELISA)和实时聚合酶链反应(PCR)分析,调查了45例巴林MS患者和45例匹配的健康对照中SARAF、基质相互作用分子1(STIM1)和Orai1的表达模式及其与钙稳态的关系。与对照组(129.82±30.82 pg/mL)相比,MS患者在疾病早期(192.26±47.00 pg/mL)和晚期(341.47±96.19 pg/mL)血清SARAF水平均显著升高(P<0.001)。MS患者中SARAF表达明显增加(3.829±0.04422对1±0;P<0.0001),而与对照组相比,STIM1(0.4324±0.01471)和Orai1(0.2963±0.02156)表达显著降低(P<0.0001)。MS早期和晚期细胞内钙水平均显著升高。这些发现表明,SARAF的逐渐升高,加上STIM1和Orai1表达的改变,可能作为MS进展的潜在生物标志物,并代表有前景的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdca/12110777/acb248b86d99/ijms-26-04520-g001.jpg

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