Literature DB >> 26551319

Decreased Expression of Enterocyte Nutrient Assimilation Genes and Proteins in the Small Intestine of Cystic Fibrosis Mouse.

Robert C De Lisle1.   

Abstract

OBJECTIVES: Cystic fibrosis (CF) has major effects on the intestinal tract with potential consequences on nutrition, but these are not fully understood. I investigated the possibility of altered enterocyte maturation in CF, as suggested by decreased enterocyte nutrient assimilation gene expression in published transcriptome analysis of the small intestine of CF mouse.
METHODS: In CF and wild-type (WT) mice, enterocyte gene/protein expression was analyzed by quantitative realtime polymerase chain reaction (qRT-PCR), enzyme histochemistry, immunohistochemistry, and Western blot. One group of mice was maintained on a control liquid diet; to manipulate the gut microbiota, a second group was treated with oral antibiotics; to improve hydration of the gut lumen, a third group was given a laxative drinking solution.
RESULTS: On the control diet in the CF intestine, there were decreased levels (67%-85% reduction of WT levels) of enterocyte genes/proteins. Antibiotics did not normalize the expression of enterocyte markers in the CF mouse. In contrast, the laxative treatment of CF mice significantly increased expression to near WT levels.
CONCLUSIONS: These studies suggest that the environment of the CF intestinal lumen plays a role in reduced maturation of enterocytes. Because changing the gut lumen environment can affect enterocyte maturation, this is not a cell-autonomous effect of loss of CF transmembrane conductance regulator.

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Year:  2016        PMID: 26551319     DOI: 10.1097/MPG.0000000000001030

Source DB:  PubMed          Journal:  J Pediatr Gastroenterol Nutr        ISSN: 0277-2116            Impact factor:   2.839


  6 in total

Review 1.  The Enigmatic Gut in Cystic Fibrosis: Linking Inflammation, Dysbiosis, and the Increased Risk of Malignancy.

Authors:  Millie Garg; Chee Y Ooi
Journal:  Curr Gastroenterol Rep       Date:  2017-02

2.  The intestinal virome in children with cystic fibrosis differs from healthy controls.

Authors:  Michael J Coffey; Ivan Low; Sacha Stelzer-Braid; Bernd Wemheuer; Millie Garg; Torsten Thomas; Adam Jaffe; William D Rawlinson; Chee Y Ooi
Journal:  PLoS One       Date:  2020-05-22       Impact factor: 3.240

3.  Gut Microbiota in Children With Cystic Fibrosis: A Taxonomic and Functional Dysbiosis.

Authors:  Michael J Coffey; Shaun Nielsen; Bernd Wemheuer; Nadeem O Kaakoush; Millie Garg; Bronwen Needham; Russell Pickford; Adam Jaffe; Torsten Thomas; Chee Y Ooi
Journal:  Sci Rep       Date:  2019-12-09       Impact factor: 4.379

Review 4.  The Gut-Lung Axis in Cystic Fibrosis.

Authors:  Courtney E Price; George A O'Toole
Journal:  J Bacteriol       Date:  2021-08-02       Impact factor: 3.476

5.  Consuming Genistein Improves Survival Rates in the Absence of Laxative in ΔF508-CF Female Mice.

Authors:  Ryan Lord; Nathan Fairbourn; Charisma Mylavarapu; Ammer Dbeis; Taylor Bowman; Archana Chandrashekar; Tatum Banayat; Craig A Hodges; Layla Al-Nakkash
Journal:  Nutrients       Date:  2018-10-03       Impact factor: 5.717

Review 6.  The Cross-Talk Between Gut Microbiota and Lungs in Common Lung Diseases.

Authors:  Dapeng Zhang; Sha Li; Ning Wang; Hor-Yue Tan; Zhimin Zhang; Yibin Feng
Journal:  Front Microbiol       Date:  2020-02-25       Impact factor: 5.640

  6 in total

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