» Articles » PMID: 9706056

Tubular Localization and Tissue Distribution of Peptide Transporters in Rat Kidney

Overview
Journal Pharm Res
Specialties Pharmacology
Pharmacy
Date 1998 Aug 26
PMID 9706056
Citations 27
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: To define the tubular localization and tissue distribution of PEPT1 (low-affinity, high-capacity transporter) and PEPT2 (high-affinity, low-capacity transporter) in rat kidney.

Methods: mRNA expression of PEPT1 and PEPT2 was assessed with reverse transcription-polymerase chain reaction (RT-PCR) methods using cDNA prepared from microdissected nephron segments in rat. Tissue localization of rat renal PEPT1 and PEPT2 mRNA was further assessed by in situ hybridization with radiolabeled probes.

Results: RT-PCR analysis of microdissected segments from rat nephron showed that both PEPT1 and PEPT2 are confined to a proximal tubule. While PEPT1 is specific for early regions of the proximal tubule (pars convoluta), PEPT2 is overwhelmingly but not exclusively expressed in latter regions of the proximal tubule (pars recta). All other segments along the nephron were negative for PEPT1 or PEPT2 mRNA transcripts. These finding were supported by in situ hybridization results in which PEPT1 was selectively expressed in kidney cortex and PEPT2 in the outer stripe of outer medulla.

Conclusions: Contrary to current opinion, the data suggest that peptides are handles in a sequential manner in proximal regions of the nephron, first by the low-affinity, high-capacity transport system and second by the high-affinity, low-capacity transport system.

Citing Articles

Molecular Insights to the Structure-Interaction Relationships of Human Proton-Coupled Oligopeptide Transporters (PepTs).

Luo Y, Gao J, Jiang X, Zhu L, Zhou Q, Murray M Pharmaceutics. 2023; 15(10).

PMID: 37896276 PMC: 10609898. DOI: 10.3390/pharmaceutics15102517.


Transport of Biologically Active Ultrashort Peptides Using POT and LAT Carriers.

Khavinson V, Linkova N, Kozhevnikova E, Dyatlova A, Petukhov M Int J Mol Sci. 2022; 23(14).

PMID: 35887081 PMC: 9323678. DOI: 10.3390/ijms23147733.


The Hydrogen-Coupled Oligopeptide Membrane Cotransporter Pept2 is SUMOylated in Kidney Distal Convoluted Tubule Cells.

Aroankins T, Murali S, Fenton R, Wu Q Front Mol Biosci. 2021; 8:790606.

PMID: 34881291 PMC: 8646034. DOI: 10.3389/fmolb.2021.790606.


Epigenetic regulation of intestinal peptide transporter PEPT1 as a potential strategy for colorectal cancer sensitization.

Wang Y, Wang J, Yang L, Qiu L, Hua Y, Wu S Cell Death Dis. 2021; 12(6):532.

PMID: 34031358 PMC: 8144210. DOI: 10.1038/s41419-021-03814-5.


The effect of cephalexin in influencing the pharmacokinetics of a novel drug - 5'-valyl-cytarabine hydrochloride.

Song X, Sun Y, Zhao C, He Z Asian J Pharm Sci. 2020; 12(2):143-148.

PMID: 32104323 PMC: 7032087. DOI: 10.1016/j.ajps.2016.08.003.


References
1.
Liang R, Fei Y, Prasad P, Ramamoorthy S, Han H, Yang-Feng T . Human intestinal H+/peptide cotransporter. Cloning, functional expression, and chromosomal localization. J Biol Chem. 1995; 270(12):6456-63. DOI: 10.1074/jbc.270.12.6456. View

2.
Ogihara H, Saito H, Shin B, Terado T, Takenoshita S, Nagamachi Y . Immuno-localization of H+/peptide cotransporter in rat digestive tract. Biochem Biophys Res Commun. 1996; 220(3):848-52. DOI: 10.1006/bbrc.1996.0493. View

3.
Boll M, Herget M, Wagener M, Weber W, Markovich D, Biber J . Expression cloning and functional characterization of the kidney cortex high-affinity proton-coupled peptide transporter. Proc Natl Acad Sci U S A. 1996; 93(1):284-9. PMC: 40223. DOI: 10.1073/pnas.93.1.284. View

4.
Brandsch M, Brandsch C, Prasad P, Ganapathy V, Hopfer U, Leibach F . Identification of a renal cell line that constitutively expresses the kidney-specific high-affinity H+/peptide cotransporter. FASEB J. 1995; 9(14):1489-96. DOI: 10.1096/fasebj.9.14.7589991. View

5.
Pavlova A, Boutin E, Cunha G, Sassoon D . Msx1 (Hox-7.1) in the adult mouse uterus: cellular interactions underlying regulation of expression. Development. 1994; 120(2):335-45. DOI: 10.1242/dev.120.2.335. View