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Umbilical cord extracts improve osteoporotic abnormalities of bone marrow-derived mesenchymal stem cells and promote their therapeutic effects on ovariectomised rats

机译:脐带提取物改善骨髓源性间充质干细胞的骨质疏松异常并促进其对去卵巢大鼠的治疗作用

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摘要

Bone marrow-derived mesenchymal stem cells (BM-MSCs) are the most valuable source of autologous cells for transplantation and tissue regeneration to treat osteoporosis. Although BM-MSCs are the primary cells responsible for maintaining bone metabolism and homeostasis, their regenerative ability may be attenuated in postmenopausal osteoporosis patients. Therefore, we first examined potential abnormalities of BM-MSCs in an oestrogen-deficient rat model constructed by ovariectomy (OVX-MSCs). Cell proliferation, mobilisation, and regulation of osteoclasts were downregulated in OVX-MSCs. Moreover, therapeutic effects of OVX-MSCs were decreased in OVX rats. Accordingly, we developed a new activator for BM-MSCs using human umbilical cord extracts, Wharton’s jelly extract supernatant (WJS), which improved cell proliferation, mobilisation and suppressive effects on activated osteoclasts in OVX-MSCs. Bone volume, RANK and TRACP expression of osteoclasts, as well as proinflammatory cytokine expression in bone tissues, were ameliorated by OVX-MSCs activated with WJS (OVX-MSCs-WJ) in OVX rats. Fusion and bone resorption activity of osteoclasts were suppressed in macrophage-induced and primary mouse bone marrow cell-induced osteoclasts via suppression of osteoclast-specific genes, such as Nfatc1, Clcn7, Atp6i and Dc-stamp, by co-culture with OVX-MSCs-WJ in vitro. In this study, we developed a new activator, WJS, which improved the functional abnormalities and therapeutic effects of BM-MSCs on postmenopausal osteoporosis.
机译:骨髓间充质干细胞(BM-MSC)是用于移植和组织再生以治疗骨质疏松症的最有价值的自体细胞来源。尽管BM-MSC是负责维持骨代谢和体内稳态的主要细胞,但在绝经后骨质疏松症患者中其再生能力可能会减弱。因此,我们首先在通过卵巢切除术(OVX-MSC)构建的雌激素缺乏大鼠模型中检查了BM-MSC的潜在异常。在OVX-MSC中,破骨细胞的细胞增殖,动员和调节被下调。而且,OVX-MSCs的治疗作用在OVX大鼠中降低。因此,我们使用人脐带提取物沃顿的果冻提取物上清液(WJS)开发了一种用于BM-MSC的新型活化剂,该活化剂可改善OVX-MSC中活化的破骨细胞的细胞增殖,动员和抑制作用。在OVX大鼠中,用WJS激活的OVX-MSC(OVX-MSCs-WJ)改善了破骨细胞的骨体积,RANK和TRACP表达,以及骨组织中的促炎细胞因子表达。通过与OVX-MSCs共培养,通过抑制破骨细胞特异性基因(例如Nfatc1,Clcn7,Atp6i和Dc-stamp),巨噬细胞诱导的和原代小鼠骨髓细胞诱导的破骨细胞抑制了破骨细胞的融合和骨吸收活性。 -WJ体外。在这项研究中,我们开发了一种新的活化剂WJS,可改善BM-MSC在绝经后骨质疏松症中的功能异常和治疗效果。

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