Department of Basic Medical Sciences, College of Medicine, Prince Sattam Bin Abdulaziz University, Al-Kharj, Kingdom of Saudi Arabia.
Cell Biochem Funct. 2021 Jan;39(1):148-158. doi: 10.1002/cbf.3596. Epub 2020 Nov 2.
Stem cell therapy is growing rapidly to treat numerous diseases including bone-associated diseases. Mesenchymal stem cells (MSCs) are most commonly preferred to treat bone diseases because it possesses high osteogenic potency. Though, to obtain maximum osteogenic efficiency of MSCs is challenging. Therefore, this study was planned to evaluate the osteogenic efficiency of human bone marrow derived mesenchymal stem cells (hBMSCs) by bacoside-A. This study was investigated the activity of alkaline phosphatase (ALP) and expressions of the genes specific to osteogenic regulation mainly runt-related transcription factor 2 (Runx2), osterix (Osx), osteocalcin (OCN) and collagen type Iα1 (Col I α1) in hBMSCs cultured under osteogenic conditions at different concentrations of bacoside-A for 14 days. The results of this study depicted significant upregulation in the activity of ALP and expressions of osteogenic regulator genes in bacoside-A treated cells when compared with control cells. Besides, expressions of glycogen synthase kinase-3β (GSK-3β) and Wnt/β-catenin were evaluated; these expressions were also significantly increased in bacoside-A treated cells when compared with control cells. This result provides a further supporting evidence of bacoside-A role on osteogenesis in hBMSCs. The present study suggest that bacoside-A will be applied to ameliorate the process of osteogenesis in hBMSCs to repair damaged bone structure during MSC-based therapy; this will be an excellent and auspicious treatment for bone-associated disorders including osteoporosis. Significance of the study Osteoporosis is a bone metabolic disorder characterized by an imbalance between the activity of osteoblastic bone formation and osteoclastic bone resorption that disrupts the bone microarchitecture. Current anti-osteoporotic drugs are inhibiting bone resorption, but they are unable to restore the bone structure due to extreme bone remodelling process and causes numerous side effects. The finding of natural bioactive compounds with osteogenic property is very essential for osteoporosis treatment. This study was reported that bacoside-A ameliorated osteogenic differentiation of hBMSCs through upregulation of osteogenic differentiation genes and Wnt/β-catenin signalling pathway. This result is indicating that bacoside-A may be useful for osteoporosis treatments.
干细胞疗法在治疗包括骨相关疾病在内的多种疾病方面迅速发展。间充质干细胞(MSCs)最常用于治疗骨疾病,因为它具有很高的成骨能力。然而,要获得 MSCs 的最大成骨效率是具有挑战性的。因此,本研究旨在通过 Bacoside-A 来评估人骨髓间充质干细胞(hBMSCs)的成骨效率。本研究在成骨条件下,研究了不同浓度 Bacoside-A 培养 14 天后对 hBMSCs 的碱性磷酸酶(ALP)活性和主要 Runt 相关转录因子 2(Runx2)、osterix(Osx)、骨钙素(OCN)和胶原 Iα1(Col Iα1)等成骨调节基因表达的影响。结果表明,与对照组相比,Bacoside-A 处理的细胞中 ALP 活性和成骨调节基因的表达显著上调。此外,还评估了糖原合酶激酶-3β(GSK-3β)和 Wnt/β-catenin 的表达;与对照组相比,Bacoside-A 处理的细胞中这些表达也显著增加。这一结果为 Bacoside-A 在 hBMSCs 成骨中的作用提供了进一步的证据。本研究表明,Bacoside-A 将应用于改善 hBMSCs 成骨过程,以修复 MSC 治疗过程中受损的骨结构;这将是治疗骨相关疾病(包括骨质疏松症)的一种极好的、有希望的治疗方法。研究意义骨质疏松症是一种骨代谢疾病,其特征是成骨细胞骨形成和破骨细胞骨吸收之间的活性失衡,破坏了骨微结构。目前的抗骨质疏松症药物是抑制骨吸收,但由于极端的骨重塑过程,它们无法恢复骨结构,并导致许多副作用。寻找具有成骨特性的天然生物活性化合物对于骨质疏松症的治疗非常重要。本研究报道 Bacoside-A 通过上调成骨分化基因和 Wnt/β-catenin 信号通路来改善 hBMSCs 的成骨分化。这一结果表明,Bacoside-A 可能对骨质疏松症的治疗有用。