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  Macrophages require distinct arginine catabolism and transport systems for proliferation and for activation

Yeramian, A., Martin, L., Arpa, L., Bertran, J., Soler, C., McLeod, C., et al. (2006). Macrophages require distinct arginine catabolism and transport systems for proliferation and for activation. European Journal of Immunology, 36, 1516-1526.

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 Creators:
Yeramian, Andrée, Author
Martin, Lorena, Author
Arpa, Luis, Author
Bertran, Joan, Author
Soler, Concepció, Author
McLeod, Carol, Author
Modolell, Manuel1, Author           
Palacín, Manuel, Author
Lloberas, Jorge, Author
Celada, Antonio, Author
Affiliations:
1Emeritus Group: Cellular Immunology, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society, ou_2243649              

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Free keywords: Activation; Arginine; Macrophages; Proliferation
 Abstract: In murine macrophages, as a result of arginine catabolism during activation, citruline is produced under the effect of IFN-γ and LPS, and ornithine and polyamines by IL-4 and IL-10. For proliferation, arginine is required from the extracellular medium and is used for protein synthesis. During activation, most arginine (>95% in 6 h) was metabolized, while under proliferation only half was incorporated into proteins. Under basal conditions, this amino acid was preferentially transported by y+L activity. During activation, arginine transport increased drastically (4-5-fold) through y+ cationic amino acid transporter (CAT) activity. By contrast, M-CSF induced only a modest increase in uptake (0.5-fold). The increase in arginine transport during activation, but not proliferation, was mediated by the SLC7A2/Cat2 gene. SLC7A1/Cat1 is constitutively expressed, and is not modified by proliferating or activating agents. M-CSF-dependent proliferation was not affected in the macrophages of SLC7A2 knockout mice; however, these cells showed a drastic reduction in the production of citruline or ornithine and polyamines during activation. The data show that a large increase in a specific transport system (CAT2) is necessary for activation-induced arginine metabolism, while arginine is in excess for the requirements of proliferation and a modest increase in transport occurs.

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Language(s): eng - English
 Dates: 2006
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 294384
 Degree: -

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Title: European Journal of Immunology
  Alternative Title : Eur. J. Immunol.
Source Genre: Journal
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Pages: - Volume / Issue: 36 Sequence Number: - Start / End Page: 1516 - 1526 Identifier: -