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激活素A在人成骨细胞细胞周期中的作用:一项初步体外实验研究。

The role of activin A in the human osteoblast cell cycle: a preliminary experimental in vitro study.

作者信息

Rosenberg N, Soudry M, Rosenberg O, Blumenfeld I, Blumenfeld Z

机构信息

Orthopaedic Surgery A Department, Rambam Medical Centre, Haifa, Israel.

出版信息

Exp Clin Endocrinol Diabetes. 2010 Nov;118(10):708-12. doi: 10.1055/s-0030-1249007. Epub 2010 Mar 2.

Abstract

Animal studies have previously shown that activin A enhances osteoblast proliferation IN VITRO and increases bone formation and bone mechanical strength IN VIVO. For the further understanding of its action in human osteoblast, we studied the pattern of a cell cycle response to the treatment with activin A. We hypothesize that activin A alters the cell cycle pattern of human osteoblast. Primary cultures of human osteoblast-like cells were treated by activin A in a biologically effective concentration (100 ng/mL). The cells in cultured samples were counted, assayed for cellular alkaline phosphatase activity and calcitonin expression, LDH activity in the medium, cellular BrdU incorporation, cell cycle cytometry and compared to untreated controls. The treated by activin A cells responded by a significant shift toward the G1 phase of the cell cycle with parallel decrease in cell death rate (lower LDH activity and less necrotic cells in cytometric analysis). The treated cells also showed a lower alkaline phosphatase activity and calcitonin expression, indicating their undifferentiated state, and didn't change their proliferation rate. The number of cells in culture increased following treatment with activin A. We show that activin A increases the net osteoblast number in culture by reducing the cell death rate without affecting the cell proliferation. These findings should be part of cellular pathways that are involved in the initial stages of bone tissue generation.

摘要

此前的动物研究表明,激活素A在体外可增强成骨细胞增殖,在体内可增加骨形成及骨机械强度。为进一步了解其在人成骨细胞中的作用,我们研究了激活素A处理后的细胞周期反应模式。我们假设激活素A会改变人成骨细胞的细胞周期模式。用人成骨样细胞原代培养物,以生物有效浓度(100 ng/mL)的激活素A进行处理。对培养样本中的细胞进行计数,检测细胞碱性磷酸酶活性、降钙素表达、培养基中的乳酸脱氢酶活性、细胞BrdU掺入情况、细胞周期流式细胞术,并与未处理的对照进行比较。用激活素A处理的细胞出现明显向细胞周期G1期的转变,同时细胞死亡率平行下降(流式细胞术分析中乳酸脱氢酶活性降低且坏死细胞减少)。处理后的细胞还表现出较低的碱性磷酸酶活性和降钙素表达,表明其处于未分化状态,且增殖率未改变。用激活素A处理后,培养物中的细胞数量增加。我们发现,激活素A通过降低细胞死亡率而增加培养物中成骨细胞的净数量,且不影响细胞增殖。这些发现应是参与骨组织生成初始阶段的细胞途径的一部分。

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