Tissue Distribution, Expression and Regulation of Urea Transporters
Nannan Li1, Janet D Klein2, Jeff M Sands2
1State Key Laboratory of Vascular Homeostasis and Remodeling, Department of Pharmacology, School of Basic Medical Sciences, Peking University, Beijing, China.
Abstract:
UT-A and UT-B families of urea transporters consist of multiple isoforms with the majority of the isoforms located in the kidney. UT-B (Slc14A1) in kidney is primarily located in the descending vasa recta. The UT-A (Slc14A2) urea transporter family comprises six distinct isoforms, three of which are predominantly found in the kidney. Specifically, UT-A1 and UT-A3 are located in the inner medullary collecting duct (IMCD), while UT-A2 is situated in the thin descending limb. These transporters play a crucial role in the renal concentration of urine. The regulation of renal urea transporter activity involves acute modifications through phosphorylation and subsequent translocation to the plasma membrane. In response to stimulation by vasopressin or hypertonicity, UT-A1 and UT-A3 accumulate in the IMCD plasma membrane. Chronic regulation of IMCD urea transporters involves hormonal modulation of protein expression levels, such as adrenal steroids, low-protein diets, electrolyte abnormalities, aging or other pathologic conditions. This chapter provides a brief overview of the tissue distribution, expression of the urea transporter isoforms, locations in the kidney, and regulation of urea transporters.
More Related Videos
13:16Characterization of Membrane Transporters by Heterologous Expression in E. coli and Production of Membrane Vesicles
Published on: December 31, 2019
11:27Methods to Study Epithelial Transport Protein Function and Expression in Native Intestine and Caco-2 Cells Grown in 3D
Published on: March 16, 2017
Related Concept Videos
Drug Elimination by Renal Route: Tubular Secretion
Urea Cycle
Tissue-Drug Binding: Localization of Drugs and its Significance
Drugs can bind to different tissue components, enhancing their distribution and localization. The factors influencing drug localization in tissues include the drug's lipophilicity, structural characteristics, tissue perfusion rate, and pH differences. These factors determine...
Renal Drug Excretion: Tubular Secretion
Pore Transport and Ion-Pair Transport
Pore transport, also known as convective transport, is a process where small molecules like urea, water, and sugars rapidly cross cell membranes as though there were channels or pores in the membrane. Although direct microscopic evidence is limited but the concept of pores or channels is widely accepted based on physiological evidence. Despite the lack of direct...
Physiology of the Genitourinary System I: Renal Blood Flow and Glomerular Filtration
