Abstract
Carnosine (beta-alanyl-histidine) and homocarnosine (gamma-aminobutyryl-histidine) are major constituents of excitable tissues, brain and skeletal muscles, but their physiological functions are yet unknown. Using primary cell culture systems, synthesis and uptake of carnosine exclusively by glial cells could be demonstrated. Uptake of carnosine was found to be mediated by a high affinity, energy-dependent dipeptide transport system, subsequently identified as the peptide transporter PepT2. With the synthesis of beta-Ala-Lys-Nepsilon-AMCA as a fluorescent reporter molecule, accumulation of this dipeptide derivative could be monitored under viable conditions not only in astroglia cells but also in folliculostellate cells of the anterior pituitary and in gonadal resident macrophages. This reporter dipeptide provided a most valuable tool to identify an intrapituitary communication system by tracing folliculostellate cells in acute slice preparation. Moreover, this substance could also be used to prepare pituitary cell cultures enriched with or depleted of folliculostellate cells that are needed for further studies.
MeSH Terms
Animals
Biological Transport/physiology
Brain/cytology,metabolism
Carnosine/analogs & derivatives,chemistry,metabolism
Cells, Cultured
Female
Macrophages/metabolism
Male
Molecular Structure
Neuroglia/cytology,metabolism
Ovary/cytology
Peptides/chemistry,metabolism
Pituitary Gland, Anterior/cytology
Testis/cytology
Chemicals
Peptides
homocarnosine
Carnosine
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Bauer Karl
Max-Planck-Institute for Experimental Endocrinology, Hannover, Germany.
[email protected]
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