Literature DB >> 20059269

Imaging of goblet cells as a marker for intestinal metaplasia of the stomach by one-photon and two-photon fluorescence endomicroscopy.

Hongchun Bao1, Alex Boussioutas, Jeremy Reynolds, Sarah Russell, Min Gu.   

Abstract

Goblet cells are a requirement for the diagnosis of intestinal metaplasia of the stomach. The gastric mucosa is lined by a monolayer of columnar epithelium with some specialization at the crypts, but there are no goblet cells in normal gastric epithelium. The appearance of goblet cells in gastric epithelium is an indicator of potential malignant progression toward adenocarcinoma. Therefore, in vivo three-dimensional imaging of goblet cells is essential for diagnoses of a premalignant stage of gastric cancers called intestinal metaplasia. We used mouse intestine, which has goblet cells, as a model of intestinal metaplasia. One-photon confocal fluorescence endomicroscopy and two-photon fluorescence endomicroscopy are employed for 3-D imaging of goblet cells. The penetration depth, the sectioning ability, and the photobleaching information of imaging are demonstrated. Both endomicroscopy techniques can three-dimensionally observe goblet cells in mouse large intestine and achieve an imaging depth of 176 microm. The two-photon fluorescence endomicroscopy shows higher resolution and contrast of the imaging sections at each depth. In addition, two-photon fluorescence endomicroscopy also has advantages of sectioning ability and less photobleaching. These results prove that two-photon fluorescence endomicroscopy is advantageous in diagnoses of a premalignant stage of gastric cancers.

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Year:  2009        PMID: 20059269     DOI: 10.1117/1.3269681

Source DB:  PubMed          Journal:  J Biomed Opt        ISSN: 1083-3668            Impact factor:   3.170


  10 in total

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2.  Three-dimensional imaging of small intestine morphology using non-linear optical microscopy and endogenous signals.

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3.  Microanatomy of the intestinal lymphatic system.

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Review 4.  Two-photon and second harmonic microscopy in clinical and translational cancer research.

Authors:  Seth W Perry; Ryan M Burke; Edward B Brown
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5.  Multi-photon vertical cross-sectional imaging with a dynamically-balanced thin-film PZT z-axis microactuator.

Authors:  Jongsoo Choi; Xiyu Duan; Haijun Li; Thomas D Wang; Kenn R Oldham
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6.  Spectrum- and time-resolved endogenous multiphoton signals reveal quantitative differentiation of premalignant and malignant gastric mucosa.

Authors:  Xi Li; Hui Li; Xingzhen He; Tingai Chen; Xianyuan Xia; Chunxia Yang; Wei Zheng
Journal:  Biomed Opt Express       Date:  2018-01-08       Impact factor: 3.732

7.  Multiphoton tomographic imaging: a potential optical biopsy tool for detecting gastrointestinal inflammation and neoplasia.

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Journal:  Cancer Prev Res (Phila)       Date:  2012-09-07

Review 8.  Progress in molecular imaging in endoscopy and endomicroscopy for cancer imaging.

Authors:  Supang Khondee; Thomas D Wang
Journal:  J Healthc Eng       Date:  2013       Impact factor: 2.682

9.  Multiphoton microscopy for ophthalmic imaging.

Authors:  Emily A Gibson; Omid Masihzadeh; Tim C Lei; David A Ammar; Malik Y Kahook
Journal:  J Ophthalmol       Date:  2011-01-03       Impact factor: 1.909

10.  Breaking the diffraction-limited resolution barrier in fiber-optical two-photon fluorescence endoscopy by an azimuthally-polarized beam.

Authors:  Min Gu; Hong Kang; Xiangping Li
Journal:  Sci Rep       Date:  2014-01-10       Impact factor: 4.379

  10 in total

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