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  • Lou, Xianfeng  (2)
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  • 1
    In: The FASEB Journal, Wiley, Vol. 37, No. 9 ( 2023-09)
    Abstract: Postmenopausal osteoporosis is associated with bone formation inhibition mediated by the impaired osteogenic differentiation potential of bone marrow mesenchymal stem cells (BMSCs). However, identifying and confirming the essential genes in the osteogenic differentiation of BMSCs and osteoporosis remain challenging. The study aimed at revealing the key gene that regulated osteogenic differentiation of BMSCs and led to osteoporosis, thus exploring its therapeutic effect in osteoporosis. In the present study, six essential genes related to the osteogenic differentiation of BMSCs and osteoporosis were identified, namely, fibrillin 2 (Fbn2), leucine‐rich repeat‐containing 17 (Lrrc17), heat shock protein b7 (Hspb7), high mobility group AT‐hook 1 (Hmga1), nexilin F‐actin‐binding protein (Nexn), and endothelial cell‐specific molecule 1 (Esm1). Furthermore, the in vivo and in vitro experiments showed that Hmga1 expression was increased during the osteogenic differentiation of rat BMSCs, while Hmga1 expression was decreased in the bone tissue of ovariectomized (OVX) rats. Moreover, the expression of osteogenic differentiation‐related genes, the activity of alkaline phosphatase (ALP), and the number of mineralized nodules were increased after Hmga1 overexpression, which was partially reversed by a Wnt signaling inhibitor (DKK1). In addition, after injecting Hmga1‐overexpressing lentivirus into the bone marrow cavity of OVX rats, the bone loss, and osteogenic differentiation inhibition of BMSCs in OVX rats were partially reversed, while osteoclast differentiation promotion of BMSCs in OVX rats was unaffected. Taken together, the present study confirms that Hmga1 prevents OVX‐induced bone loss by the Wnt signaling pathway and reveals that Hmga1 is a potential gene therapeutic target for postmenopausal osteoporosis.
    Type of Medium: Online Resource
    ISSN: 0892-6638 , 1530-6860
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2023
    detail.hit.zdb_id: 1468876-1
    SSG: 12
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  • 2
    Online Resource
    Online Resource
    American Scientific Publishers ; 2023
    In:  Journal of Biomedical Nanotechnology Vol. 19, No. 5 ( 2023-05-01), p. 747-757
    In: Journal of Biomedical Nanotechnology, American Scientific Publishers, Vol. 19, No. 5 ( 2023-05-01), p. 747-757
    Abstract: Spinal cord injury (SCI) is frequently accompanied by sensorimotor deficits that persist for years in the absence of effective treatments. Biochanin A (BCA), a natural isoflavone, belongs to phytoestrogen. BCA can perform multiple functions, but its role of SCI is unclear. The purpose of this study was to explore the impact and mechanism of BCA on microglia by simulating SCI with lipopolysaccharide (LPS) in vitro . The results showed that BCA inhibited microglial apoptosis and promoted SCI repair by inducing M2 microglia polarization and secretion of anti-inflammatory factors. Notably, the efficacy of the above-mentioned effects of BCA was correlated with autophagic flux. We further explored the underlying molecular mechanisms and confirmed the critical importance of toll-like receptor 4 (TLR4) in counteracting the effect of BCA on LPS-BV-2 cells. The TLR4/NF- κ B pathway was shown to promote M1 microglial polarization, inflammation and cellular apoptosis. In conclusion, BCA blocks the TLR4/NF- κ B pathway to inhibit M1 microglial polarization and apoptosis after SCI. This study is expected to provide the scientific basis for the SCI.
    Type of Medium: Online Resource
    ISSN: 1550-7033
    Language: English
    Publisher: American Scientific Publishers
    Publication Date: 2023
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