Developmental regulation of Na(+)/H(+) exchanger expression in fetal and neonatal mice.

Am J Physiol Heart Circ Physiol

Department of Biochemistry, University of Alberta, Canadian Institute of Health Research Membrane Protein Group, Edmonton, Alberta, Canada T6G 2H7.

Published: July 2002

AI Article Synopsis

  • The study investigates how the expression of the Na(+)/H(+) exchanger (specifically the NHE1 isoform) changes during fetal and neonatal development.
  • Researchers created transgenic mice to track NHE1 expression using a green fluorescent protein marker linked to the NHE1 promoter.
  • Findings indicated that NHE1 transcription and protein levels vary based on tissue type and developmental stage, with peak expression observed in the heart and liver around 12-15 days of age, and a notable increase in protein levels occurring post-embryonic day 18.

Article Abstract

We examined the hypothesis that Na(+)/H(+) exchanger expression is regulated during fetal and neonatal development and differentiation. To examine transcriptional regulation of the NHE1 isoform of the Na(+)/H(+) exchanger, transgenic mice were created that contained the mouse NHE1 promoter driving expression of green fluorescent protein. The level of NHE1 transcription varied between tissues and with the stage of embryonic development. The highest expression was in the heart and liver of 12- to 15-day-old mice, and this declined with age. To examine Na(+)/H(+) exchanger protein levels, we immunoblotted mouse tissues from 18-day-old embryos, neonates, and adults. Protein levels increased after embryonic day 18 and peaked at 14 days of age in the heart, lung, liver, kidney, and brain. The greatest rise in NHE1 protein expression occurred in the heart, whereas the smallest increase was in the brain. The results suggest that Na(+)/H(+) exchanger transcription and protein levels are controlled in a tissue-specific and time-dependent manner during development.

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http://dx.doi.org/10.1152/ajpheart.00042.2002DOI Listing

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