Using Ex Vivo Live Imaging to Investigate Cell Divisions and Movements During Mouse Dental Renewal

被引:0
|
作者
Thooyamani, Abinaya Sundari [1 ]
Shahin, Elias [2 ]
Takano, Sanako [1 ]
Sharir, Amnon [2 ]
Hu, Jimmy K. [1 ,3 ]
机构
[1] Univ Calif Los Angeles, Sch Dent, Los Angeles, CA 90095 USA
[2] Hebrew Univ Jerusalem, Inst Biomed & Oral Res, Fac Dent Med, Jerusalem, Israel
[3] Univ Calif Los Angeles, Mol Biol Inst, Los Angeles, CA 90095 USA
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2023年 / 200期
基金
以色列科学基金会;
关键词
STEM-CELLS; AMELOBLAST-PROGENITORS; TOOTH DEVELOPMENT; SHEAR-STRESS; RAT INCISOR; REPORTER; GROWTH; DYNAMICS; REPAIR; GENES;
D O I
10.3791/66020
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The continuously growing mouse incisor is emerging as a highly tractable model system to investigate the regulation of adult epithelial and mesenchymal stem cells and tooth regeneration. These progenitor populations actively divide, move, and differentiate to maintain tissue homeostasis and regenerate lost cells in a responsive manner. However, traditional analyses using fixed tissue sections could not capture the dynamic processes of cellular movements and interactions, limiting our ability to study their regulations. This paper describes a protocol to maintain whole mouse incisors in an explant culture system and live-track dental epithelial cells using multiphoton timelapse microscopy. This technique adds to our existing toolbox for dental research and allows investigators to acquire spatiotemporal information on cell behaviors and organizations in a living tissue. We anticipate that this methodology will help researchers further explore mechanisms that control the dynamic cellular processes taking place during both dental renewal and regeneration.
引用
收藏
页数:18
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