首页> 外文期刊>Calcified tissue international. >TGF beta-1 mRNA expression and proliferation of human osteoblastic cells in nonosteoporotic and osteoporotic women under influence of TGF beta-1 and IGF-I.
【24h】

TGF beta-1 mRNA expression and proliferation of human osteoblastic cells in nonosteoporotic and osteoporotic women under influence of TGF beta-1 and IGF-I.

机译:非骨质疏松和骨质疏松妇女在TGFβ-1和IGF-I影响下,TGFβ-1mRNA的表达和人类成骨细胞的增殖。

获取原文
获取原文并翻译 | 示例
           

摘要

Currently, primary osteoporosis is the most frequent metabolic disease in women after menopause [1]. The resulting loss of bone mass is accompanied by an increased risk of skeletal fragility. One reason for the development of osteoporosis might be an impaired function of mature osteoblasts. To evaluate the involvement of specific growth factors in bone remodeling, cell cultures of osteoblastic cells derived from nonosteoporotic and osteoporotic postmenopausal women were established. The influences of TGF beta-1 and IGF-I on proliferation and mRNA expression of TGF beta-1 were investigated by [3H]-thymidine incorporation and competitive RT-PCR. We found IGF-I to have no significant effect on proliferation in cells of osteoporotic and nonosteoporotic patients. In contrast, differences were found in TGF beta-1 mRNA expression after application of IGF-I. Application of TGF beta-1 enhanced its own mRNA expression in both groups in a similar manner. Whereas the proliferation of cells of nonosteoporotic patients was inhibited by (10(-10) M) TGF beta-1, this treatment led to an increased proliferation of cells of osteoporotic patients.
机译:目前,原发性骨质疏松症是绝经后女性中最常见的代谢疾病[1]。导致的骨量流失伴随着骨骼脆性风险的增加。骨质疏松症发展的原因之一可能是成熟成骨细胞的功能受损。为了评估特定生长因子在骨重塑中的作用,建立了非骨质疏松和绝经后骨质疏松妇女的成骨细胞细胞培养。通过[3 H]-胸苷掺入和竞争性RT-PCR研究了TGF-β-1和IGF-I对TGF-β-1增殖和mRNA表达的影响。我们发现IGF-I对骨质疏松和非骨质疏松患者的细胞增殖没有显着影响。相反,在施用IGF-1后发现TGFβ-1mRNA表达有差异。 TGF beta-1的应用以相似的方式在两组中增强了其自身的mRNA表达。非骨质疏松症患者的细胞增殖受到(10(-10)M)TGFβ-1的抑制,但这种治疗导致骨质疏松症患者的细胞增殖增加。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号