Literature DB >> 9394122

Regional restriction of alcohol/retinol dehydrogenases along the mouse gastrointestinal epithelium.

R J Haselbeck1, G Duester.   

Abstract

The gastrointestinal tract is a major site of alcohol dehydrogenase (ADH) activity in humans and rodents. Because class I ADH (ADH-I) and class IV ADH (ADH-IV), but not class III ADH (ADH-III), function as retinol dehydrogenases in vitro and may thus participate in retinoid signaling needed for epithelial differentiation, the aim of this study was to determine the localization of these enzymes along the gastrointestinal tract. Specific antibodies were used to examine the tissue distribution of all three known classes of mouse ADH by Western blotting, and cellular localization was determined by immunohistochemistry. ADH-I was detected primarily in the intestine, liver, kidney, adrenal, and uterus, with detection of ADH-III in all tissues examined, and detection of ADH-IV primarily in the esophagus, stomach, adrenal, skin, ovary, and epididymis. Along the gastrointestinal tract, ADH-III was not specifically localized, whereas ADH-I was localized exclusively in the villus epithelium of the small intestine and absorptive epithelium of the large intestine, with ADH-IV being localized exclusively in the basal and suprabasal epithelial cells of the esophagus and gastric pit surface epithelium of the stomach. The ADH localization patterns observed are consistent with ADH-I and ADH-IV, but not ADH-III, functioning physiologically in retinol metabolism needed for epithelial differentiation. Our results further suggest that the functions of ADH-I and ADH-IV are regionally restricted to the lower and upper components, respectively, of the gastrointestinal epithelium, a finding that may relate to the different efficiencies of these two enzymes for retinol oxidation, as well as to the different susceptibilities of the upper and lower digestive tracts for ethanol-induced cancers.

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Year:  1997        PMID: 9394122

Source DB:  PubMed          Journal:  Alcohol Clin Exp Res        ISSN: 0145-6008            Impact factor:   3.455


  11 in total

1.  Inhibition of retinol oxidation by ethanol in the rat liver and colon.

Authors:  A Parlesak; I Menzl; A Feuchter; J C Bode; C Bode
Journal:  Gut       Date:  2000-12       Impact factor: 23.059

2.  Changes in the activity of alcohol dehydrogenase isoenzymes during the estrus cycle in the vagina of the rat.

Authors:  C Nowak; I P Maly; D Sasse
Journal:  Histochem J       Date:  2000-08

3.  Distinct functions for Aldh1 and Raldh2 in the control of ligand production for embryonic retinoid signaling pathways.

Authors:  R J Haselbeck; I Hoffmann; G Duester
Journal:  Dev Genet       Date:  1999

Review 4.  Retinoic Acid Synthesis and Degradation.

Authors:  Natalia Y Kedishvili
Journal:  Subcell Biochem       Date:  2016

5.  Stimulation of retinoic acid production and growth by ubiquitously expressed alcohol dehydrogenase Adh3.

Authors:  Andrei Molotkov; Xiaohong Fan; Louise Deltour; Mario H Foglio; Silvia Martras; Jaume Farrés; Xavier Parés; Gregg Duester
Journal:  Proc Natl Acad Sci U S A       Date:  2002-04-16       Impact factor: 11.205

6.  Expression of alcohol dehydrogenase 3 in tissue and cultured cells from human oral mucosa.

Authors:  J J Hedberg; J O Höög; J A Nilsson; Z Xi; A Elfwing; R C Grafström
Journal:  Am J Pathol       Date:  2000-11       Impact factor: 4.307

7.  Distinct retinoid metabolic functions for alcohol dehydrogenase genes Adh1 and Adh4 in protection against vitamin A toxicity or deficiency revealed in double null mutant mice.

Authors:  Andrei Molotkov; Louise Deltour; Mario H Foglio; Arnold E Cuenca; Gregg Duester
Journal:  J Biol Chem       Date:  2002-02-08       Impact factor: 5.157

Review 8.  Retinoic acid in the immune system.

Authors:  Karina Pino-Lagos; Micah J Benson; Randolph J Noelle
Journal:  Ann N Y Acad Sci       Date:  2008-11       Impact factor: 5.691

9.  Two zebrafish alcohol dehydrogenases share common ancestry with mammalian class I, II, IV, and V alcohol dehydrogenase genes but have distinct functional characteristics.

Authors:  Mark J Reimers; Mark E Hahn; Robert L Tanguay
Journal:  J Biol Chem       Date:  2004-07-01       Impact factor: 5.157

10.  Targeted disruption of Aldh1a1 (Raldh1) provides evidence for a complex mechanism of retinoic acid synthesis in the developing retina.

Authors:  Xiaohong Fan; Andrei Molotkov; Shin-Ichi Manabe; Christine M Donmoyer; Louise Deltour; Mario H Foglio; Arnold E Cuenca; William S Blaner; Stuart A Lipton; Gregg Duester
Journal:  Mol Cell Biol       Date:  2003-07       Impact factor: 4.272

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