H+/peptide transporter (PEPT2) is expressed in human epidermal keratinocytes and is involved in skin oligopeptide transport
Creators
- 1. DHC Corporation Laboratories, Division 2, 2-42 Hamada, Mihama-ku, Chiba 261-0025 (Japan)
- 2. Department of Biological Chemistry, Division of Applied Life Science, Graduate School of Life and Environmental Sciences, Osaka Prefecture University, 1-1 Gakuen-cho, Naka-ku, Sakai 599-8531 (Japan)
Description
Peptide transporter 2 (PEPT2) is a member of the proton-coupled oligopeptide transporter family, which mediates the cellular uptake of oligopeptides and peptide-like drugs. Although PEPT2 is expressed in many tissues, its expression in epidermal keratinocytes remains unclear. We investigated PEPT2 expression profile and functional activity in keratinocytes. We confirmed PEPT2 mRNA expression in three keratinocyte lines (normal human epidermal keratinocytes (NHEKs), immortalized keratinocytes, and malignant keratinocytes) by reverse transcription-polymerase chain reaction (RT-PCR) and quantitative real-time RT-PCR. In contrast to PEPT1, PEPT2 expression in the three keratinocytes was similar or higher than that in HepG2 cells, used as PEPT2-positive cells. Immunolocalization analysis using human skin showed epidermal PEPT2 localization. We studied keratinocyte transport function by measuring the oligopeptide content using liquid chromatography/tandem mass spectrometry. Glycylsarcosine uptake in NHEKs was pH-dependent, suggesting that keratinocytes could absorb small peptides in the presence of an inward H+ gradient. We also performed a skin-permeability test of several oligopeptides using skin substitute, suggesting that di- and tripeptides pass actively through the epidermis. In conclusion, PEPT2 is expressed in keratinocytes and involved in skin oligopeptide uptake. -- Highlights: •PEPT2 is expressed in keratinocytes, which are more common than other skin cells. •Immunolocalization analysis using human skin revealed epidermal PEPT2 localization. •Keratinocytes could absorb small peptides in the presence of an inward H+ gradient. •Di- and tripeptide pass actively through the epidermis.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.bbrc.2016.05.093Additional details
Identifiers
- DOI
- 10.1016/j.bbrc.2016.05.093;
- PII
- S0006-291X(16)30801-4;
Publishing Information
- Journal Title
- Biochemical and Biophysical Research Communications
- Journal Volume
- 475
- Journal Issue
- 4
- Journal Page Range
- p. 335-341
- ISSN
- 0006-291X
- CODEN
- BBRCA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48043464
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- COLLAGEN; EPIDERMIS; LIQUID COLUMN CHROMATOGRAPHY; MASS SPECTROSCOPY; MESSENGER-RNA; PEPTIDES; PERMEABILITY; PH VALUE; POLYMERASE CHAIN REACTION; TRANSCRIPTION; UPTAKE
- Descriptors DEC
- ANIMAL TISSUES; BODY; CHROMATOGRAPHY; EPITHELIUM; GENE AMPLIFICATION; NUCLEIC ACIDS; ORGANIC COMPOUNDS; ORGANS; PHYSICAL PROPERTIES; PROTEINS; RNA; SCLEROPROTEINS; SEPARATION PROCESSES; SKIN; SPECTROSCOPY
Optional Information
- Copyright
- Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.