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秦皮乙素促进成骨细胞分化及基质小泡介导的矿化。

Aesculetin Accelerates Osteoblast Differentiation and Matrix-Vesicle-Mediated Mineralization.

机构信息

Department of Food and Nutrition and Korean Institute of Nutrition, Hallym University, Chuncheon 24252, Korea.

出版信息

Int J Mol Sci. 2021 Nov 17;22(22):12391. doi: 10.3390/ijms222212391.

Abstract

The imbalance between bone resorption and bone formation in favor of resorption results in bone loss and deterioration of bone architecture. Osteoblast differentiation is a sequential event accompanying biogenesis of matrix vesicles and mineralization of collagen matrix with hydroxyapatite crystals. Considerable efforts have been made in developing naturally-occurring plant compounds, preventing bone pathologies, or enhancing bone regeneration. Coumarin aesculetin inhibits osteoporosis through hampering the ruffled border formation of mature osteoclasts. However, little is known regarding the effects of aesculetin on the impairment of matrix vesicle biogenesis. MC3T3-E1 cells were cultured in differentiation media with 1-10 μM aesculetin for up to 21 days. Aesculetin boosted the bone morphogenetic protein-2 expression, and alkaline phosphatase activation of differentiating MC3T3-E1 cells. The presence of aesculetin strengthened the expression of collagen type 1 and osteoprotegerin and transcription of Runt-related transcription factor 2 in differentiating osteoblasts for 9 days. When ≥1-5 μM aesculetin was added to differentiating cells for 15-18 days, the induction of non-collagenous proteins of bone sialoprotein II, osteopontin, osteocalcin, and osteonectin was markedly enhanced, facilitating the formation of hydroxyapatite crystals and mineralized collagen matrix. The induction of annexin V and PHOSPHO 1 was further augmented in ≥5 μM aesculetin-treated differentiating osteoblasts for 21 days. In addition, the levels of tissue-nonspecific alkaline phosphatase and collagen type 1 were further enhanced within the extracellular space and on matrix vesicles of mature osteoblasts treated with aesculetin, indicating matrix vesicle-mediated bone mineralization. Finally, aesculetin markedly accelerated the production of thrombospondin-1 and tenascin C in mature osteoblasts, leading to their adhesion to preformed collagen matrix. Therefore, aesculetin enhanced osteoblast differentiation, and matrix vesicle biogenesis and mineralization. These findings suggest that aesculetin may be a potential osteo-inductive agent preventing bone pathologies or enhancing bone regeneration.

摘要

成骨细胞分化是一个伴随基质小泡生物发生和胶原基质矿化形成羟磷灰石晶体的连续事件。人们已经做出了相当大的努力来开发天然存在的植物化合物,预防骨病理学,或增强骨再生。香豆素七叶亭通过阻碍成熟破骨细胞的皱襞边缘形成来抑制骨质疏松症。然而,关于七叶亭对基质小泡生物发生损伤的影响知之甚少。MC3T3-E1 细胞在含有 1-10 μM 七叶亭的分化培养基中培养长达 21 天。七叶亭促进了骨形态发生蛋白-2 的表达,并激活了分化的 MC3T3-E1 细胞中的碱性磷酸酶。在分化的成骨细胞中,存在七叶亭可增强胶原 I 型和护骨素的表达以及 Runt 相关转录因子 2 的转录 9 天。当 1-5 μM 的七叶亭添加到分化细胞中 15-18 天时,骨唾液蛋白 II、骨桥蛋白、骨钙素和骨连蛋白的非胶原蛋白的诱导明显增强,促进了羟磷灰石晶体和矿化胶原基质的形成。在分化的成骨细胞中添加≥5 μM 的七叶亭 21 天,进一步增强了 annexin V 和 PHOSPHO 1 的诱导。此外,组织非特异性碱性磷酸酶和胶原 I 型的水平在成熟成骨细胞的细胞外空间和基质小泡中进一步增强,表明基质小泡介导的骨矿化。最后,七叶亭显著加速了成熟成骨细胞中血小板反应蛋白-1 和 tenascin C 的产生,导致它们附着到预先形成的胶原基质上。因此,七叶亭增强了成骨细胞的分化以及基质小泡的生物发生和矿化。这些发现表明,七叶亭可能是一种潜在的骨诱导剂,可预防骨病理学或增强骨再生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a65e/8621655/c2dbcdc235ab/ijms-22-12391-g001.jpg

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