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通过延时视频显微镜和免疫组织化学定量分析β细胞复制和凋亡时,将频率转换为速率的因素的研究进展。

Development of factors to convert frequency to rate for beta-cell replication and apoptosis quantified by time-lapse video microscopy and immunohistochemistry.

作者信息

Saisho Yoshifumi, Manesso Erica, Gurlo Tatyana, Huang Chang-Jiang, Toffolo Gianna M, Cobelli Claudio, Butler Peter C

机构信息

Larry Hillblom Islet Research Center, UCLA David Geffen School of Medicine, 900 Weyburn Place #A, Los Angeles, CA 90024-2852, USA.

出版信息

Am J Physiol Endocrinol Metab. 2009 Jan;296(1):E89-96. doi: 10.1152/ajpendo.90697.2008. Epub 2008 Oct 21.

Abstract

An obstacle to development of methods to quantify beta-cell turnover from pancreas tissue is the lack of conversion factors for the frequency of beta-cell replication or apoptosis detected by immunohistochemistry to rates of replication or apoptosis. We addressed this obstacle in islets from 1-mo-old rats by quantifying the relationship between the rate of beta-cell replication observed directly by time-lapse video microscopy (TLVM) and the frequency of beta-cell replication in the same islets detected by immunohistochemistry using antibodies against Ki67 and insulin in the same islets fixed immediately after TLVM. Similarly, we quantified the rate of beta-cell apoptosis by TLVM and then the frequency of apoptosis in the same islets using TdT-mediated dUTP nick-end labeling and insulin. Conversion factors were developed by regression analysis. The conversion factor from Ki67 labeling frequency (%) to actual replication rate (%events/h) is 0.025 +/- 0.003 h(-1). The conversion factor from TdT-mediated dUTP nick-end labeling frequency (%) to actual apoptosis rate (%events/h) is 0.41 +/- 0.05 h(-1). These conversion factors will permit development of models to evaluate beta-cell turnover in fixed pancreas tissue.

摘要

从胰腺组织定量β细胞更新方法发展的一个障碍是,缺乏将免疫组织化学检测到的β细胞复制或凋亡频率转化为复制或凋亡速率的转换因子。我们通过量化延时视频显微镜(TLVM)直接观察到的β细胞复制速率与使用抗Ki67和胰岛素抗体在TLVM后立即固定的同一胰岛中通过免疫组织化学检测到的β细胞复制频率之间的关系,解决了1月龄大鼠胰岛中的这一障碍。同样,我们通过TLVM量化β细胞凋亡速率,然后使用TdT介导的dUTP缺口末端标记和胰岛素量化同一胰岛中的凋亡频率。通过回归分析得出转换因子。从Ki67标记频率(%)到实际复制速率(%事件/小时)的转换因子为0.025±0.003 h⁻¹。从TdT介导的dUTP缺口末端标记频率(%)到实际凋亡速率(%事件/小时)的转换因子为0.41±0.05 h⁻¹。这些转换因子将有助于开发评估固定胰腺组织中β细胞更新的模型。

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