Two-photon microscopy of Paneth cells in the small intestine of live mice

被引:0
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作者
Won Hyuk Jang
Areum Park
Taejun Wang
Chan Johng Kim
Hoonchul Chang
Bo-Gie Yang
Myoung Joon Kim
Seung-Jae Myung
Sin-Hyeog Im
Myoung Ho Jang
You-Me Kim
Ki Hean Kim
机构
[1] Pohang University of Science and Technology (POSTECH),Division of Integrative Biosciences and Biotechnology
[2] Yonsei University College of Medicine,507 Avison Biomedical Research Center, Severance Biomedical Research Institute
[3] University of Ulsan College of Medicine,Department of Ophthalmology
[4] Asan Medical Center,Department of Gastroenterology
[5] University of Ulsan College of Medicine,Academy of Immunology and Microbiology
[6] Asan Medical Center,Graduate School of Medical Science and Engineering
[7] Institute for Basic Science (IBS),Department of Mechanical Engineering
[8] Korea Advanced Institute of Science and Technology,undefined
[9] Pohang University of Science and Technology (POSTECH),undefined
来源
关键词
Paneth Cells; Paneth Cell Granules; Intestinal Crypts; Moxifloxacin Ophthalmic Solution; LysoTracker;
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摘要
Paneth cells are one of the principal epithelial cell types in the small intestine, located at the base of intestinal crypts. Paneth cells play key roles in intestinal host-microbe homeostasis via granule secretion, and their dysfunction is implicated in pathogenesis of several diseases including Crohn’s disease. Despite their physiological importance, study of Paneth cells has been hampered by the limited accessibility and lack of labeling methods. In this study, we developed a simple in vivo imaging method of Paneth cells in the intact mouse small intestine by using moxifloxacin and two-photon microscopy (TPM). Moxifloxacin, an FDA-approved antibiotic, was used for labeling cells and its fluorescence was strongly observed in Paneth cell granules by TPM. Moxifloxacin labeling of Paneth cell granules was confirmed by molecular counterstaining. Comparison of Paneth cells in wild type, genetically obese (ob/ob), and germ-free (GF) mice showed different granule distribution. Furthermore, Paneth cell degranulation was observed in vivo. Our study suggests that TPM with moxifloxacin labeling can serve as a useful tool for studying Paneth cell biology and related diseases.
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