Literature DB >> 25301986

Computer aided classification of cell nuclei in the gastrointestinal tract by volume and principal axis.

Ann M Sagstetter1, Jon J Camp1, Matthew S Lurken1, Joseph H Szurszewski1, Gianrico Farrugia1, Simon J Gibbons1, Richard A Robb1.   

Abstract

Normal function of the gastrointestinal tract involves the coordinated activity of several cell types Human disorders of motor function of the gastrointestinal tract are often associated with changes in the number of these cells. For example, in diabetic patients, abnormalities in gastrointestinal transit are associated with changes in nerves and interstitial cells of Cajal (ICC), two key cells that generate and regulate motility. ICC are cells of mesenchymal origin that function as pacemakers and amplify neuronal signals in the gastrointestinal tract. Quantifying the changes in number of specific cell types in tissues from patients with motility disorders is challenging and requires immunolabeling for specific antigens. The shape of nuclei differs between the cell types in the wall of the gastrointestinal tract. Therefore the objective of this study was to determine whether cell nuclei can be classified by analyzing the 3D morphology of the nuclei. Furthermore, the orientation of the long axis of nuclei changes within and between the muscle layers. These features can be used to classify and differentially label the nuclei in confocal volume images of the tissue by computing the principal axis of the coordinates of the set of voxels forming each nucleus and thereby to identify cells by their nuclear morphology. Using this approach, we were able to separate and quantify nuclei in the smooth muscle layers of the tissue. Therefore we conclude that computer-aided classification of cell nuclei can be used to identify changes in the cell types expressed in gastrointestinal smooth muscle.

Entities:  

Keywords:  cell differentiation; confocal microscopy; feature extraction; principal component analysis

Year:  2007        PMID: 25301986      PMCID: PMC4188371          DOI: 10.1117/12.710274

Source DB:  PubMed          Journal:  Proc SPIE Int Soc Opt Eng        ISSN: 0277-786X


  10 in total

1.  WZsGreen/+: a new green fluorescent protein knock-in mouse model for the study of KIT-expressing cells in gut and cerebellum.

Authors:  Mira Wouters; Karine Smans; Jean-Marie Vanderwinden
Journal:  Physiol Genomics       Date:  2005-06-14       Impact factor: 3.107

2.  The use of constitutive nuclear oncoproteins to count neurons in the enteric nervous system of the guinea pig.

Authors:  E J Parr; K A Sharkey
Journal:  Cell Tissue Res       Date:  1994-08       Impact factor: 5.249

3.  Prevalence of gastrointestinal symptoms associated with diabetes mellitus: a population-based survey of 15,000 adults.

Authors:  P Bytzer; N J Talley; M Leemon; L J Young; M P Jones; M Horowitz
Journal:  Arch Intern Med       Date:  2001-09-10

4.  Loss of interstitial cells of cajal and inhibitory innervation in insulin-dependent diabetes.

Authors:  C L He; E E Soffer; C D Ferris; R M Walsh; J H Szurszewski; G Farrugia
Journal:  Gastroenterology       Date:  2001-08       Impact factor: 22.682

5.  Remodeling of networks of interstitial cells of Cajal in a murine model of diabetic gastroparesis.

Authors:  T Ordög; I Takayama; W K Cheung; S M Ward; K M Sanders
Journal:  Diabetes       Date:  2000-10       Impact factor: 9.461

6.  Pan-colonic decrease in interstitial cells of Cajal in patients with slow transit constipation.

Authors:  G L Lyford; C-L He; E Soffer; T L Hull; S A Strong; A J Senagore; L J Burgart; T Young-Fadok; J H Szurszewski; G Farrugia
Journal:  Gut       Date:  2002-10       Impact factor: 23.059

7.  Kit/stem cell factor receptor-induced phosphatidylinositol 3'-kinase signalling is not required for normal development and function of interstitial cells of Cajal in mouse gastrointestinal tract.

Authors:  S J Gibbons; A Rich; M A Distad; S M Miller; P F Schmalz; J H Szurszewski; L Sha; P Blume-Jensen; G Farrugia
Journal:  Neurogastroenterol Motil       Date:  2003-12       Impact factor: 3.598

8.  Acquisition of neuronal and glial markers by neural crest-derived cells in the mouse intestine.

Authors:  Heather M Young; Annette J Bergner; Thomas Müller
Journal:  J Comp Neurol       Date:  2003-01-27       Impact factor: 3.215

9.  Insulin restores neuronal nitric oxide synthase expression and function that is lost in diabetic gastropathy.

Authors:  C C Watkins; A Sawa; S Jaffrey; S Blackshaw; R K Barrow; S H Snyder; C D Ferris
Journal:  J Clin Invest       Date:  2000-08       Impact factor: 14.808

10.  Spatial and temporal patterns of c-kit-expressing cells in WlacZ/+ and WlacZ/WlacZ mouse embryos.

Authors:  F Bernex; P De Sepulveda; C Kress; C Elbaz; C Delouis; J J Panthier
Journal:  Development       Date:  1996-10       Impact factor: 6.868

  10 in total

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