In situ hybridization and immunolocalization of concentrative and equilibrative nucleoside transporters in the human intestine, liver, kidneys, and placenta

• Published in: American journal of physiology. Regulatory, integrative and comparative physiology Vol. 293; no. 5; pp. R1809 - R1822
• Main Authors: Govindarajan, Rajgopal, Bakken, Aimee H, Hudkins, Kelly L, Lai, Yurong, Casado, F. Javier, Pastor-Anglada, Marcal, Tse, Chung-Ming, Hayashi, Jun, Unadkat, Jashvant D
• Format: Journal Article
• Language: English
• Published: United States American Physiological Society 01.11.2007
• Subjects: Adult; Digestive system; Equilibrative Nucleoside Transport Proteins - metabolism; Female; Fetus - metabolism; Fluorescence in situ hybridization; Humans; Immunohistochemistry; In Situ Hybridization; Intestines - metabolism; Kidney - metabolism; Kidneys; Liver; Liver - metabolism; Male; Pharmacology; Placenta - metabolism; Pregnancy; Reproductive system; RNA, Messenger - biosynthesis; Tissue Distribution
• ISSN: 0363-6119; 1522-1490
• DOI: 10.1152/ajpregu.00293.2007

Departments of 1 Pharmaceutics, 2 Biology, and 3 Pathology, University of Washington, Seattle, Washington; 4 Department of Biochemistry and Molecular Biology, Institute of Biomedicine, University of Barcelona and Centro de Investigacíon, Biomédica en Red-Enfermedades Hepáticasay Digestivas, Barcelona, Spain; and 5 Division of Gastroenterology, Department of Medicine, Johns Hopkins University School of Medicine and 6 Department of Pharmaceutical Sciences, University of Maryland, Baltimore, Maryland Submitted 27 April 2007 ; accepted in final form 24 August 2007 To better understand the role of human equilibrative (hENTs) and concentrative (hCNTs) nucleoside transporters in physiology and pharmacology, we investigated the regional, cellular, and spatial distribution of two hCNTs (hCNT1 and hCNT2) and two hENTs (hENT1 and hENT2) in four human tissues. Using in situ hybridization and immunohistochemical techniques, we found that the duodenum expressed hCNT1 and hCNT2 mRNAs in enterocytes and hENT1 and hENT2 mRNAs in crypt cells. In these cells, the hCNT and hENT proteins were predominantly localized in the apical and lateral membrane, respectively. Hepatocytes expressed higher levels of mRNAs of hENT1, hCNT1, and hENT2 than of hCNT2 and expressed all these proteins at hepatocyte cell borders and in the cytoplasm. While the kidney expressed hCNT1 and hCNT2 mRNAs in the proximal tubules, hENT1 and hENT2 mRNAs were present in the distal tubules, glomeruli, endothelial cells, and vascular smooth muscle cells. Proximal tubules adjacent to corticomedullary junctions expressed hENT1, hCNT1, and hCNT2 mRNA. Immunolocalization studies revealed predominant localization of hCNTs in the brush-border membrane of the proximal tubular epithelial cells and hENTs in the basolateral membrane of the distal tubular epithelial cells. Chorionic villi sections of human term placenta expressed mRNAs and proteins for hENT1 and hENT2 but only mRNA for hCNT2. Immunolocalization studies showed presence of hENT1 in the brush-border membrane of the syncytiotrophoblasts. These data are critical for a better understanding of the role of nucleoside transporters in the physiological and pharmacological effects of nucleosides and nucleoside drugs, respectively. expression; localization; human tissue Address for reprint requests and other correspondence: J. D. Unadkat, Dept. of Pharmaceutics, Univ. of Washington, Box 357610, Seattle, WA 98195 (e-mail: jash{at}u.washington.edu )