## Abstract MIP26/AQP0 is the major lens fiber membrane protein and has been reported to interact with many other lens components including crystallins, lipid, and cytoskeletal proteins. Regarding crystallins, many previous reports indicate that MIP26/AQP0 interacts with either only Ξ±βcrystallin or
From cells to tissues: Fluorescence confocal microscopy in the study of histological samples
β Scribed by Pietro Transidico; Marco Bianchi; Maria Capra; Pier Giuseppe Pelicci; Mario Faretta
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 210 KB
- Volume
- 64
- Category
- Article
- ISSN
- 1059-910X
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Our knowledge of the genetic mechanisms controlling cell proliferation and differentiation usually originates from in vitro cultured cell line models. However, the definition of the molecular switches involved in control of homeostasis and the understanding of the changes occurring in neoplastic transformation require looking at single cells as the components of a complex tissue network. Histological examination of tissue samples can gain a substantial amount of information from highβresolution fluorescence analysis. In particular, confocal microscopy can help in the definition of functional pathways using multiparameter analysis. In this report, we present acquisition and analysis procedures to obtain highβresolution data from tissue sections. Confocal microscopy coupled to computational restoration, statistical evaluation of spatial correlations, and morphological analysis over large tissue areas were applied to colorectal samples providing a molecular fingerprint of the biological differences inferred from classical histological examination. Microsc. Res. Tech. 64:89β95, 2004. Β© 2004 WileyβLiss, Inc.
π SIMILAR VOLUMES
The study of biological systems in their real environmental conditions is crucial to decipher the true image of structures and processes underlying their functionality. In this regard, development of non-invasive optical techniques that do not require labelling, such as the investigation of tissue e
for immunofluorescence microscopic investigation of the plant cytoskeleton, especially during mitosis. These advantages include: (1) unimpeded access of antibody probes, (2) confocal-like imaging without the expense of confocal equipment, (3) maintenance of organ architecture as well as intracellula
## Background: In paramecium primaurelia, an exconjugant cell can produce two lines with different mating capacities. mating type ii cells can form a higher food vacuole number and digest the nutrient taken up in a shorter time; thus, mating type ii cells grow at a faster rate than do mating type i