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

被引:16
|
作者
Jang, Won Hyuk [1 ]
Park, Areum [1 ]
Wang, Taejun [1 ]
Kim, Chan Johng [1 ]
Chang, Hoonchul [1 ]
Yang, Bo-Gie [2 ]
Kim, Myoung Joon [3 ]
Myung, Seung-Jae [4 ]
Im, Sin-Hyeog [1 ,5 ]
Jang, Myoung Ho [5 ]
Kim, You-Me [6 ]
Kim, Ki Hean [1 ,7 ]
机构
[1] Pohang Univ Sci & Technol POSTECH, Div Integrat Biosci & Biotechnol, 77 Cheongam Ro, Pohang 37673, Gyeongbuk, South Korea
[2] Yonsei Univ, Coll Med, Severance Biomed Res Inst, Avison Biomed Res Ctr 507, 50-1 Yonsei Ro, Seoul 03722, South Korea
[3] Univ Ulsan, Asan Med Ctr, Coll Med, Dept Ophthalmol, 88 Olymp Ro,43 Gil, Seoul 05505, South Korea
[4] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Gastroenterol, 88 Olymp Ro,43 Gil, Seoul 05505, South Korea
[5] Acad Immunol & Microbiol, IBS, 77 Cheongam ro, Pohang 37673, Gyeongbuk, South Korea
[6] Korea Adv Inst Sci & Technol, Grad Sch Med Sci & Engn, 291 Daehak Ro, Daejeon 34141, South Korea
[7] Pohang Univ Sci & Technol POSTECH, Dept Mech Engn, 77 Cheongam Ro, Pohang 37673, Gyeongbuk, South Korea
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
基金
新加坡国家研究基金会;
关键词
CROHNS-DISEASE; STEM-CELLS; MOXIFLOXACIN; COLON; PHARMACOKINETICS; FLUORESCENCE; PENETRATION; ACTIVATION; RISK; GENE;
D O I
10.1038/s41598-018-32640-7
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
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.
引用
收藏
页数:10
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