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1.
Biochim Biophys Acta ; 1511(1): 17-27, 2001 Mar 09.
Artigo em Inglês | MEDLINE | ID: mdl-11248201

RESUMO

A family of anion exchangers (AEs) including AE1, AE2 and AE3 has been described. AE3 gene has been shown to encode two alternatively spliced isoforms termed as bAE3 (brain subtype) and cAE3 (cardiac subtype). The identity of the AE(s) involved in the human intestinal NaCl absorption is not fully understood. Current studies were undertaken to identify the AE isoforms expressed in the human intestine, to define their regional and vertical axis (crypt vs. surface cells) distribution, and to elucidate their membrane localization in the epithelial cells along the entire length of the human intestine. Our studies utilizing reverse transcription (RT)-PCR with total RNA extracted from pinch biopsies from various regions of the human intestine demonstrate that AE2 and bAE3 but not AE1 or cAE3 were expressed in all the regions of the human intestine. Utilizing in situ RT-PCR, we demonstrated that the message of AE2 was expressed throughout the vertical surface--crypt axis of the colon. Our Western blotting studies demonstrated that AE2 and bAE3 are localized to the basolateral but not the apical membranes of the intestinal epithelial cells from the human ileum and colon. In conclusion, our results demonstrated that in the human intestine, AE2 and bAE3, but not AE1 or cAE3, are expressed throughout the tract with the highest expression in the colon compared to the ileum and jejunum. Both the isoforms were found to be localized to the basolateral but not the apical membranes of the epithelial cells. We speculate that, in the human intestine, AE2 and bAE3 may be the 'housekeeping' isoforms, and the apical AE, the potential candidate for chloride absorption, remains to be identified.


Assuntos
Proteínas de Transporte de Ânions , Mucosa Intestinal/metabolismo , Proteínas de Membrana/metabolismo , Antiporters/metabolismo , Antiportadores de Cloreto-Bicarbonato , Colo/metabolismo , Células Epiteliais/metabolismo , Humanos , Íleo/metabolismo , Immunoblotting , Jejuno/metabolismo , Proteínas de Membrana/análise , Isoformas de Proteínas/análise , Isoformas de Proteínas/metabolismo , RNA Mensageiro/análise , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Proteínas SLC4A
3.
Am J Physiol ; 271(3 Pt 1): G483-93, 1996 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-8843774

RESUMO

The identity of Na+/H+ exchanger (NHE) isoforms in the human small intestine and colon and their role in vectorial Na+ absorption are not known. The present studies were undertaken to examine the regional and vertical axis distribution of NHE-1, NHE-2, and NHE-3 mRNA in the human intestine. Ribonuclease protection assays were used to quantitate the levels of mRNA of these isoforms in various regions of the human intestine. In situ hybridization technique was used to localize NHE-2 and NHE-3 mRNA in the colon. The NHE-1 isoform message was present uniformly throughout the length of the human intestine. In contrast, mRNA levels for human NHE-2 and NHE-3 isoforms demonstrated significant regional differences. The NHE-3 abundance was found in decreasing order: ileum > jejunum > proximal colon = distal colon. The NHE-2 message level in the distal colon was significantly higher than in the proximal colon but was evenly distributed in the small intestine. In addition, NHE-2 mRNA was present in surface epithelial cells as well as in cells of the crypt region, suggesting the presence of NHE-2 message throughout the vertical axis of the colonic crypts. In contrast, NHE-3 mRNA was localized to surface colonocytes in the proximal colon. On the basis of this tissue-specific localization of NHE-2 and NHE-3 mRNA, it can be speculated that the relative contribution of NHE-2 and NHE-3 isoforms in Na+ absorption in the human intestine may be region specific, and these putative apical isoforms may be differentially regulated.


Assuntos
Colo/metabolismo , Intestino Delgado/metabolismo , RNA Mensageiro/análise , Trocadores de Sódio-Hidrogênio/metabolismo , Sequência de Aminoácidos , Animais , Humanos , Hibridização In Situ , Dados de Sequência Molecular , Coelhos , Ratos , Alinhamento de Sequência , Trocador 3 de Sódio-Hidrogênio , Trocadores de Sódio-Hidrogênio/análise
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