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测定胰腺切片中的胰岛β细胞质量、凋亡、增殖和单个胰岛β细胞大小。

Determining Beta Cell Mass, Apoptosis, Proliferation, and Individual Beta Cell Size in Pancreatic Sections.

机构信息

CIBER of Diabetes and Metabolic Diseases, CIBERDEM, Barcelona, Spain.

Bellvitge Biomedical Research Institute, IDIBELL, Barcelona, Spain.

出版信息

Methods Mol Biol. 2020;2128:313-337. doi: 10.1007/978-1-0716-0385-7_21.

Abstract

Pancreatic beta cells have a significant remodeling capacity which plays an essential role in the maintenance of glucose homeostasis. Beta cell apoptosis, replication, size, dedifferentiation, and (neo)generation contribute to the beta cell mass regulation. However, the extent of their respective contribution varies significantly depending on the specific condition, and it is the balance among them that determines the eventual change in beta cell mass. Thus, the study of the pancreatic beta cell mass regulation requires the determination of all these factors. In this chapter, we describe the quantification of beta cell replication based on the incorporation of thymidine analogs into replicated DNA strands and on the expression of Ki67 antigen and phosphorylation of histone H3. Beta cell apoptosis is analyzed by the TUNEL technique, and beta cell mass and cross-sectional area of individual beta cells are determined by computerized image processing methods.

摘要

胰岛β细胞具有显著的重塑能力,这对于维持葡萄糖内环境稳定至关重要。β细胞凋亡、复制、大小、去分化和(新)生成有助于调节β细胞数量。然而,它们各自的贡献程度因具体情况而异,决定β细胞数量最终变化的是它们之间的平衡。因此,研究胰岛β细胞数量的调节需要确定所有这些因素。在这一章中,我们描述了基于胸腺嘧啶核苷类似物掺入复制的 DNA 链以及 Ki67 抗原表达和组蛋白 H3 磷酸化来定量检测β细胞复制的方法。通过 TUNEL 技术分析β细胞凋亡,通过计算机图像处理方法确定单个β细胞的β细胞数量和横截面积。

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