Use of fluorescence imaging to investigate the structure and function of intestinal M cells

被引:42
作者
Buda, A [1 ]
Sands, C
Jepson, MA
机构
[1] Univ Padua, Dept Surg & Gastroenterol Sci, I-35010 Padua, Italy
[2] Univ Bristol, Sch Med Sci, Cell Imaging Facil, Bristol BS8 1TD, Avon, England
[3] Univ Bristol, Sch Med Sci, Dept Biochem, Bristol BS8 1TD, Avon, England
基金
英国惠康基金; 英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
M cells; microparticles; Peyer's patches; confocal microscopy; fluorescence imaging;
D O I
10.1016/j.addr.2004.07.014
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Fluorescence imaging technology can be applied to many aspects of cell biology ranging from the analysis of specific markers in cells and tissues to the biological actions and distribution of fluorescent proteins or particles in living cells. In this review, we examine the role of fluorescence imaging, in conjunction with other microscopical techniques, to study sites of uptake of material across the gastrointestinal epithelium. We will focus primarily on intestinal M cells, specialised antigen-sampling cells in the epithelium of the gut-associated lymphoid tissue (GALT), including Peyer's patches. In addition to their importance as sites for uptake of inert material, and hence their potential as a route of delivery of vaccines, etc., M cells are also a major site of infection by a range of microbial pathogens. The application of new fluorescence imaging technologies has expanded our knowledge on the structure, development and function of these fascinating cells. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:123 / 134
页数:12
相关论文
共 92 条
[1]   STABILITY OF LIPOSOMES IN-VITRO AND THEIR UPTAKE BY RAT PEYER PATCHES FOLLOWING ORAL-ADMINISTRATION [J].
ARAMAKI, Y ;
TOMIZAWA, H ;
HARA, T ;
YACHI, K ;
KIKUCHI, H ;
TSUCHIYA, S .
PHARMACEUTICAL RESEARCH, 1993, 10 (08) :1228-1231
[2]   Penetration of M cells and destruction of Peyer's patches by Yersinia enterocolitica: An ultrastructural and histological study [J].
Autenrieth, IB ;
Firsching, R .
JOURNAL OF MEDICAL MICROBIOLOGY, 1996, 44 (04) :285-294
[3]   Oral delivery of pathogens from the intestine to the nervous system [J].
Baird, AW ;
Campion, DP ;
O'Brien, L ;
Brayden, DJ .
JOURNAL OF DRUG TARGETING, 2004, 12 (02) :71-78
[4]   Kinetics of particle uptake in the domes of Peyer's patches [J].
Beier, R ;
Gebert, A .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1998, 275 (01) :G130-G137
[5]   PINOCYTOSIS BY EPITHELIUM ASSOCIATED WITH LYMPHOID FOLLICLES IN BURSA OF FABRICIUS, APPENDIX, AND PEYERS PATCHES - ELECTRON-MICROSCOPIC STUDY [J].
BOCKMAN, DE ;
COOPER, MD .
AMERICAN JOURNAL OF ANATOMY, 1973, 136 (04) :455-477
[6]  
Borghesi C, 1999, LAB INVEST, V79, P1393
[7]   Apical membrane receptors on intestinal M cells: potential targets for vaccine delivery [J].
Brayden, DJ ;
Baird, AW .
ADVANCED DRUG DELIVERY REVIEWS, 2004, 56 (06) :721-726
[8]   In vivo measurement of gene expression, angiogenesis and physiological function in tumors using multiphoton laser scanning microscopy [J].
Brown, EB ;
Campbell, RB ;
Tsuzuki, Y ;
Xu, L ;
Carmeliet, P ;
Fukumura, D ;
Jain, RK .
NATURE MEDICINE, 2001, 7 (07) :864-868
[9]  
BYE WA, 1984, GASTROENTEROLOGY, V86, P789
[10]   Polymerized liposomes as potential oral vaccine carriers: Stability and bioavailability [J].
Chen, HM ;
Torchilin, V ;
Langer, R .
JOURNAL OF CONTROLLED RELEASE, 1996, 42 (03) :263-272