Mechanistic studies on δ-aminolevulinic acid uptake and efflux in a mammary adenocarcinoma cell line

δ-aminolevulinic acid (ALA) is the precursor in the biosynthesis of porphyrins. The knowledge of both the regulation of ALA entrance and efflux from the cells and the control of porphyrin biosynthesis is essential to improve ALA-mediated photodynamic therapy. In this work, we studied the regulation...

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Autores principales: Correa García, S., Casas, A., Perotti, C., Batlle, A., Bermúdez Moretti, M.
Formato: Artículo publishedVersion
Publicado: 2003
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00070920_v89_n1_p173_CorreaGarcia
https://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_00070920_v89_n1_p173_CorreaGarcia_oai
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spelling I28-R145-paper_00070920_v89_n1_p173_CorreaGarcia_oai2024-08-16 Correa García, S. Casas, A. Perotti, C. Batlle, A. Bermúdez Moretti, M. 2003 δ-aminolevulinic acid (ALA) is the precursor in the biosynthesis of porphyrins. The knowledge of both the regulation of ALA entrance and efflux from the cells and the control of porphyrin biosynthesis is essential to improve ALA-mediated photodynamic therapy. In this work, we studied the regulation of ALA uptake and efflux by endogenously accumulated ALA and/or porphyrins in murine mammary adenocarcinoma cells. Under our set of conditions, the haem synthesis inhibitor succinyl acetone completely prevented porphobilinogen and porphyrin synthesis from ALA, and led to an increase in the intracellular ALA pool. However, neither intracellular ALA nor porphyrin pools regulate ALA uptake or efflux during the first 15 min of the process. Based on temperature dependence data, ALA but not γ-aminobutyric acid (GABA) efflux is mediated by a diffusion mechanism. Moreover, the addition of extracellular GABA not only did not influence the rate of ALA efflux but on the contrary it affected ALA uptake, showing the contribution of a saturable mechanism for the uptake, but not for the efflux of ALA from the cells. © 2003 Cancer Research UK. Fil:Correa García, S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Casas, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Perotti, C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Batlle, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Bermúdez Moretti, M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. application/pdf http://hdl.handle.net/20.500.12110/paper_00070920_v89_n1_p173_CorreaGarcia info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar Br. J. Cancer 2003;89(1):173-177 δ-aminolevulinic acid ALA efflux ALA uptake Photodynamic therapy 4 aminobutyric acid aminolevulinic acid heme derivative porphobilinogen porphyrin succinylacetone animal cell article breast adenocarcinoma cancer cell culture cell transport controlled study diffusion heme synthesis mouse nonhuman photodynamic therapy priority journal protein function protein protein interaction protein transport temperature dependence Adenocarcinoma Aminolevulinic Acid Animals gamma-Aminobutyric Acid Mammary Neoplasms, Animal Mice Photochemotherapy Photosensitizing Agents Porphyrins Tumor Cells, Cultured Mechanistic studies on δ-aminolevulinic acid uptake and efflux in a mammary adenocarcinoma cell line info:eu-repo/semantics/article info:ar-repo/semantics/artículo info:eu-repo/semantics/publishedVersion https://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_00070920_v89_n1_p173_CorreaGarcia_oai
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-145
collection Repositorio Digital de la Universidad de Buenos Aires (UBA)
topic δ-aminolevulinic acid
ALA efflux
ALA uptake
Photodynamic therapy
4 aminobutyric acid
aminolevulinic acid
heme derivative
porphobilinogen
porphyrin
succinylacetone
animal cell
article
breast adenocarcinoma
cancer cell culture
cell transport
controlled study
diffusion
heme synthesis
mouse
nonhuman
photodynamic therapy
priority journal
protein function
protein protein interaction
protein transport
temperature dependence
Adenocarcinoma
Aminolevulinic Acid
Animals
gamma-Aminobutyric Acid
Mammary Neoplasms, Animal
Mice
Photochemotherapy
Photosensitizing Agents
Porphyrins
Tumor Cells, Cultured
spellingShingle δ-aminolevulinic acid
ALA efflux
ALA uptake
Photodynamic therapy
4 aminobutyric acid
aminolevulinic acid
heme derivative
porphobilinogen
porphyrin
succinylacetone
animal cell
article
breast adenocarcinoma
cancer cell culture
cell transport
controlled study
diffusion
heme synthesis
mouse
nonhuman
photodynamic therapy
priority journal
protein function
protein protein interaction
protein transport
temperature dependence
Adenocarcinoma
Aminolevulinic Acid
Animals
gamma-Aminobutyric Acid
Mammary Neoplasms, Animal
Mice
Photochemotherapy
Photosensitizing Agents
Porphyrins
Tumor Cells, Cultured
Correa García, S.
Casas, A.
Perotti, C.
Batlle, A.
Bermúdez Moretti, M.
Mechanistic studies on δ-aminolevulinic acid uptake and efflux in a mammary adenocarcinoma cell line
topic_facet δ-aminolevulinic acid
ALA efflux
ALA uptake
Photodynamic therapy
4 aminobutyric acid
aminolevulinic acid
heme derivative
porphobilinogen
porphyrin
succinylacetone
animal cell
article
breast adenocarcinoma
cancer cell culture
cell transport
controlled study
diffusion
heme synthesis
mouse
nonhuman
photodynamic therapy
priority journal
protein function
protein protein interaction
protein transport
temperature dependence
Adenocarcinoma
Aminolevulinic Acid
Animals
gamma-Aminobutyric Acid
Mammary Neoplasms, Animal
Mice
Photochemotherapy
Photosensitizing Agents
Porphyrins
Tumor Cells, Cultured
description δ-aminolevulinic acid (ALA) is the precursor in the biosynthesis of porphyrins. The knowledge of both the regulation of ALA entrance and efflux from the cells and the control of porphyrin biosynthesis is essential to improve ALA-mediated photodynamic therapy. In this work, we studied the regulation of ALA uptake and efflux by endogenously accumulated ALA and/or porphyrins in murine mammary adenocarcinoma cells. Under our set of conditions, the haem synthesis inhibitor succinyl acetone completely prevented porphobilinogen and porphyrin synthesis from ALA, and led to an increase in the intracellular ALA pool. However, neither intracellular ALA nor porphyrin pools regulate ALA uptake or efflux during the first 15 min of the process. Based on temperature dependence data, ALA but not γ-aminobutyric acid (GABA) efflux is mediated by a diffusion mechanism. Moreover, the addition of extracellular GABA not only did not influence the rate of ALA efflux but on the contrary it affected ALA uptake, showing the contribution of a saturable mechanism for the uptake, but not for the efflux of ALA from the cells. © 2003 Cancer Research UK.
format Artículo
Artículo
publishedVersion
author Correa García, S.
Casas, A.
Perotti, C.
Batlle, A.
Bermúdez Moretti, M.
author_facet Correa García, S.
Casas, A.
Perotti, C.
Batlle, A.
Bermúdez Moretti, M.
author_sort Correa García, S.
title Mechanistic studies on δ-aminolevulinic acid uptake and efflux in a mammary adenocarcinoma cell line
title_short Mechanistic studies on δ-aminolevulinic acid uptake and efflux in a mammary adenocarcinoma cell line
title_full Mechanistic studies on δ-aminolevulinic acid uptake and efflux in a mammary adenocarcinoma cell line
title_fullStr Mechanistic studies on δ-aminolevulinic acid uptake and efflux in a mammary adenocarcinoma cell line
title_full_unstemmed Mechanistic studies on δ-aminolevulinic acid uptake and efflux in a mammary adenocarcinoma cell line
title_sort mechanistic studies on δ-aminolevulinic acid uptake and efflux in a mammary adenocarcinoma cell line
publishDate 2003
url http://hdl.handle.net/20.500.12110/paper_00070920_v89_n1_p173_CorreaGarcia
https://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_00070920_v89_n1_p173_CorreaGarcia_oai
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AT casasa mechanisticstudiesondaminolevulinicaciduptakeandeffluxinamammaryadenocarcinomacellline
AT perottic mechanisticstudiesondaminolevulinicaciduptakeandeffluxinamammaryadenocarcinomacellline
AT batllea mechanisticstudiesondaminolevulinicaciduptakeandeffluxinamammaryadenocarcinomacellline
AT bermudezmorettim mechanisticstudiesondaminolevulinicaciduptakeandeffluxinamammaryadenocarcinomacellline
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