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骨细胞生物学:其对骨质疏松症的影响

Osteocyte biology: its implications for osteoporosis.

作者信息

Bonewald L F

机构信息

Department of Oral Biology, University of Missouri at Kansas City School of Dentistry, Kansas City, MO 64108-2784, USA.

出版信息

J Musculoskelet Neuronal Interact. 2004 Mar;4(1):101-4.

Abstract

Osteocyte viability may play a significant role in the maintenance and integrity of bone. Bone loss due to osteoporosis may be due in part to osteocyte cell death. We have identified a factor that will protect both osteoblasts and osteocytes from cell death due to agents known to be responsible for various forms of osteoporosis. Not only does estrogen preserve osteoblast and osteocyte viability, but so does a molecule called CD40Ligand. This molecule is expressed on activated T lymphocytes, human dendritic cells, and human vascular endothelial cells, whereas its receptor CD40 is expressed on normal epithelium, B cells, and dendritic cells. CD40Ligand protects osteoblasts and the MLO-Y4 osteocyte-like cells against apoptosis induced by glucocorticoids, tumor necrosis factor alpha or etoposide. As tumor necrosis factor a has been shown to be responsible for post-menopausal bone loss and glucocorticoids induce dramatic bone loss, this finding has important implications with regards to potential therapy for both post-menopausal and steroid-induced osteoporosis.

摘要

骨细胞的存活能力可能在骨骼的维持和完整性方面发挥重要作用。骨质疏松导致的骨质流失可能部分归因于骨细胞死亡。我们已经鉴定出一种因子,它可以保护成骨细胞和骨细胞免受已知导致各种形式骨质疏松的因素所引起的细胞死亡。雌激素不仅能维持成骨细胞和骨细胞的存活能力,一种名为CD40配体的分子也能做到。该分子在活化的T淋巴细胞、人树突状细胞和人血管内皮细胞上表达,而其受体CD40则在正常上皮细胞、B细胞和树突状细胞上表达。CD40配体可保护成骨细胞和MLO-Y4骨细胞样细胞免受糖皮质激素、肿瘤坏死因子α或依托泊苷诱导的细胞凋亡。由于肿瘤坏死因子α已被证明与绝经后骨质流失有关,且糖皮质激素会导致严重的骨质流失,这一发现对于绝经后骨质疏松症和类固醇诱导的骨质疏松症的潜在治疗具有重要意义。

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