Department of Trauma Orthopedics, The First Affiliated Hospital of Wannan Medical College, Yijishan Hospital, No.2, Zheshan Xi Road, Wuhu, 241001, Anhui, People's Republic of China.
Mol Biol Rep. 2022 Dec;49(12):11913-11924. doi: 10.1007/s11033-022-08003-x. Epub 2022 Oct 15.
Aloe polysaccharide (AP) is a type of an active macromolecule of Aloe vera, which contributes to its function. However, whether AP possesses anti-osteoporosis properties is unknown.
Adipose-derived stromal cells were treated with different concentrations of AP. Early and late osteogenesis were, respectively, evaluated by ALP and Alizarin Red S staining. The effect of AP on the processes of adipogenesis inhibition in ADSCs was analyzed by oil red O staining. Western blot was used to assess the expression of osteogenic and adipogenic related factors. Then, Noggin was administered to further confirm the mechanism by which AP promotes the osteogenesis of ADSCs. Finally, 40 female SD rats were classified into a bilateral laparotomy group (Sham group) and three bilateral ovariectomy groups: OVX group, OVX + AP group, and OVX + AP + Noggin group. The bilateral rat femurs were collected to perform micro-CT scanning, HE, Masson trichrome, and Oil red O staining.
The results indicated that AP could increase ALP expression and calcium deposition. Through molecular mechanisms, AP promotes the protein expression of COL1A1, OPN, and ALP in ADSCs, but downregulates the expression of PPARγ. Also, AP directs ADSCs' fate by stimulating the BMP2/Smads signaling pathway. In vivo, the rat AP-treated had more trabecular bone than the OVX rat, indicating partial protection from cancellous bone loss after treatment with AP.
Our results show that AP may promote osteogenesis of ADSCs through BMP-2/Smads signaling pathway and inhibits lipogenic differentiation. Thus, AP might be a promising alternative medicine to treat postmenopausal osteoporosis.
芦荟多糖(AP)是芦荟中一种具有活性的大分子物质,对其功能有重要贡献。然而,AP 是否具有抗骨质疏松特性尚不清楚。
用不同浓度的 AP 处理脂肪来源的基质细胞。通过碱性磷酸酶(ALP)和茜素红 S 染色分别评估早期和晚期成骨作用。油红 O 染色分析 AP 对 ADSCs 脂肪生成抑制过程的影响。Western blot 用于评估成骨和脂肪生成相关因子的表达。然后,给予 Noggin 进一步证实 AP 促进 ADSCs 成骨的机制。最后,将 40 只雌性 SD 大鼠分为双侧剖腹组(Sham 组)和 3 个双侧卵巢切除组:OVX 组、OVX+AP 组和 OVX+AP+Noggin 组。收集双侧大鼠股骨进行 micro-CT 扫描、HE、Masson 三色和油红 O 染色。
结果表明,AP 可以增加 ALP 表达和钙沉积。通过分子机制,AP 促进 ADSCs 中 COL1A1、OPN 和 ALP 的蛋白表达,但下调 PPARγ 的表达。此外,AP 通过刺激 BMP2/Smads 信号通路来指导 ADSCs 的命运。在体内,AP 处理的大鼠比 OVX 大鼠有更多的小梁骨,表明在用 AP 治疗后部分保护了松质骨丢失。
我们的结果表明,AP 可能通过 BMP-2/Smads 信号通路促进 ADSCs 的成骨作用,并抑制脂肪生成分化。因此,AP 可能是治疗绝经后骨质疏松症的一种有前途的替代药物。