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携带bcl-2基因慢病毒感染人原代卵巢颗粒细胞的凋亡***☆

王雪峰 谭峰 陈燕英 刘木彪 何援利

中国组织工程研究Issue(28):5209-5215,7.
中国组织工程研究Issue(28):5209-5215,7.DOI:10.3969/j.issn.2095-4344.2013.28.018

携带bcl-2基因慢病毒感染人原代卵巢颗粒细胞的凋亡***☆

Apoptosis of human primary ovarian granulose cells infected with lentivirus carrying bcl-2 gene

王雪峰 1谭峰 1陈燕英 1刘木彪 1何援利1

作者信息

  • 1. 南方医科大学附属珠江医院妇产科,广东省广州市 510282
  • 折叠

摘要

Abstract

BACKGROUND: Lentivirus can infect divided and undivided cells. It remains uncertain whether the lentivirus can successful y infect primary ovarian granulosa cells. OBJECTIVE: To investigate infecting ratio and cel apoptosis of lentivirus carrying bcl-2 gene in primary human ovarian granulose cells cultured in vitro. METHODS: The lentiviral vector carrying bcl-2 gene was constructed using molecular biology, and packaged into lentivirus with high titer. The resulting recombinant lentivirus carrying bcl-2 genes were then used to infect primary human ovarian granulosa cells in vitro at different multiplicity of infection, 10, 50, 100, 200, and 400. Infection efficiency and cel proliferation were observed at 24, 48, 72, and 96 hours fol owing infection. Cel apoptosis was detected by flow cytometry, and bcl-2 gene transcription was assessed using reverse transcription PCR. RESULTS AND CONCLUSION: Primary human ovarian granulosa cells adhered at 24 hours, and exhibited polygon- or fusiform-shape and colony-like growth. When multiplicity of infection was 100, cel appearance and growth remained unchanged, and infection efficiency was high, which reached the peak up to 72 hours. Moreover, the positive rate was up to 60% in granulosa cells. Lentivirus carrying bcl-2 gene could increase expression of Bcl-2 protein and inhibit apoptosis of primary ovarian granulosa cells.

关键词

组织构建/组织构建细胞学实验/bcl-2 基因/慢病毒/卵巢颗粒细胞/细胞凋亡/基因转染/载体构建/卵巢早衰/增强型绿色荧光蛋白基因/国家自然科学基金

分类

医药卫生

引用本文复制引用

王雪峰,谭峰,陈燕英,刘木彪,何援利..携带bcl-2基因慢病毒感染人原代卵巢颗粒细胞的凋亡***☆[J].中国组织工程研究,2013,(28):5209-5215,7.

基金项目

Supported by:the National Natural Science Foundation of China in 2010, No.81041101* ()

the Natural Science Foundation of Guangdong Province in 2010, No.10451051501004704* ()

the Science and Technology Program of Guangzhou in 2011, No.2011J4100087* ()

中国组织工程研究

OACSCDCSTPCD

2095-4344

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