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International Immunology Advance Access originally published online on December 19, 2007
International Immunology 2008 20(2):215-222; doi:10.1093/intimm/dxm137
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© The Japanese Society for Immunology. 2007. All rights reserved. For permissions, please e-mail: journals.permissions@oxfordjournals.org

Functional phenotype of macrophages depends on assay procedures

Chi-Shiun Chiang1, Fang-Hsin Chen1, Ji-Hong Hong2, Pei-Shin Jiang1, Hsiang-Ling Huang1, Chun-Chieh Wang2 and William H. McBride3

1 Department of Biomedical Engineering and Environmental Sciences, National Tsing Hua University, 101 Section 2, Kuang-Fu Road, Hsinchu 30013, Taiwan
2 Department of Radiation Oncology, Chang Gung Memorial Hospital, Tao-Yuan 30033, Taiwan
3 Department Radiation Oncology, David Geffen School for Medicine, University of California, Los Angeles, Los Angeles, CA, USA

Correspondence to: C.-S. Chiang; E-mail: cschiang{at}mx.nthu.edu.tw

Macrophages display different phenotypes that can switch in response to their micro-environment. In our earlier study (Chiang, C. S., Liu, W. C. and Jung, S. M., 2005. Compartmental responses after thoracic irradiation of mice: strain differences. Int. J. Radiat. Oncol. Biol. Phys. 62:862) on radiation-induced cytokine expression in lung lavage samples, there was a suggestion that the procedures used to harvest lung macrophages affected the profiles they expressed. To further explore this issue, we examined gene expression by cell populations, mainly macrophages, isolated by lavage from lung and peritoneal cavity following either in vivo or in vitro stimulation with LPS, IFN-{gamma} or irradiation. We found that expression of mRNA for tumor necrosis factor-alpha, IL-1{alpha}/β and IL-6 varied several fold depending on whether the assay was performed on cells immediately after isolation or after in vitro manipulation. The relative level of inducible nitric oxide synthase (iNOS) to arginase I (Arg I), which is frequently used as index of the M1 versus M2 functional macrophage phenotype, also varied. LPS stimulation in vivo was able to change the profile from Arg I expression to one where the iNOS pathway became dominant, but was unable to do this in vitro. This contrasts with the ability of IFN-{gamma} to generate an iNOS-dominant pathway in vitro, but not in vivo. This study cautions that the expression of inflammatory cytokines and the iNOS to Arg I ratio, which is often used as an index of their functional capacity, varies with the experimental conditions.

Keywords: arginase, cytokines, nitric oxide synthase


Transmitting editor: A. Falus

Received 10 October 2007, accepted 25 November 2007.


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