S. Galván-peña, O. Neill, and L. , Metabolic reprograming in macrophage polarization, Front Immunol, vol.5, pp.420-426, 2014.

S. Huang, A. Smith, B. Everts, M. Colonna, E. Pearce et al., Metabolic Reprogramming Mediated by the mTORC2-IRF4 Signaling Axis Is Essential for Macrophage Alternative Activation, Immunity, vol.45, issue.4, pp.45817-830, 2016.
DOI : 10.1016/j.immuni.2016.09.016

M. Mehta, S. Weinberg, and N. Chandel, Mitochondrial control of immunity: beyond ATP, Nature Reviews Immunology, vol.17, issue.10, 2017.
DOI : 10.1038/nature17399

J. Rodríguez-prados, P. Través, J. Cuenca, D. Rico, J. Aragonés et al., Substrate Fate in Activated Macrophages: A Comparison between Innate, Classic, and Alternative Activation, The Journal of Immunology, vol.185, issue.1, pp.605-619, 2010.
DOI : 10.4049/jimmunol.0901698

D. Vats, L. Mukundan, J. Odegaard, L. Zhang, K. Smith et al., Oxidative metabolism and PGC-1?? attenuate macrophage-mediated inflammation, Cell Metabolism, vol.4, issue.1, pp.13-24, 2006.
DOI : 10.1016/j.cmet.2006.05.011
URL : https://doi.org/10.1016/j.cmet.2006.08.006

Y. Liu, W. Chen, L. Minze, J. Kubiak, X. Li et al., Dissonant response of M0/M2 and M1 bone-marrow-derived macrophages to RhoA pathway interference, Cell and Tissue Research, vol.135, issue.3, pp.707-720, 2016.
DOI : 10.1016/j.thromres.2015.03.020
URL : https://hal.archives-ouvertes.fr/hal-01439380

Y. Liu, L. Minze, L. Mumma, X. Li, R. Ghobrial et al., Mouse macrophage polarity and ROCK1 activity depend on RhoA and non-apoptotic Caspase 3, Experimental Cell Research, vol.341, issue.2, pp.225-261, 2016.
DOI : 10.1016/j.yexcr.2016.02.004

Y. Liu, N. Tejpal, J. You, X. Li, R. Ghobrial et al., ROCK inhibition impedes macrophage polarity and functions, Cellular Immunology, vol.300, pp.54-62, 2016.
DOI : 10.1016/j.cellimm.2015.12.005

F. Mcwhorter, T. Wang, P. Nguyen, T. Chung, and W. Liu, Modulation of macrophage phenotype by cell shape, Proceedings of the National Academy of Sciences, vol.93, issue.3, pp.17253-17258, 2013.
DOI : 10.1016/j.biomaterials.2013.02.065

I. Boldogh and L. Pon, Interactions of mitochondria with the actin cytoskeleton, Biochimica et Biophysica Acta (BBA) - Molecular Cell Research, vol.1763, issue.5-6, pp.450-462, 2006.
DOI : 10.1016/j.bbamcr.2006.02.014

B. Cunniff, A. Mckenzie, N. Heintz, and A. Howe, AMPK activity regulates trafficking of mitochondria to the leading edge during cell migration and matrix invasion, Molecular Biology of the Cell, vol.54, issue.5A, pp.2662-2674, 2016.
DOI : 10.1016/j.molcel.2014.04.024

B. Cunniff, Miro1-mediated mitochondrial positioning shapes intracellular energy gradients required for cell migration, Mol Biol Cell, vol.28, pp.2159-2169, 2017.

N. Georgakopoulos, G. Wells, and M. Campanella, The pharmacological regulation of cellular mitophagy, Nature Chemical Biology, vol.5, issue.2
DOI : 10.1016/j.biocel.2016.08.019

M. Kalbácová, M. Vrbacký, Z. Drahota, and Z. Melková, Comparison of the effect of mitochondrial inhibitors on mitochondrial membrane potential in two different cell lines using flow cytometry and spectrofluorometry, Cytometry A, vol.52, pp.110-116, 2003.

N. Smolina, J. Bruton, A. Kostareva, and T. Sejersen, Assaying Mitochondrial Respiration as an Indicator of Cellular Metabolism and Fitness, Methods Mol Biol, vol.1, pp.1601-79, 2017.
DOI : 10.1038/nprot.2012.048

E. Schon, Isolation of a cDNA clone encoding subunit IV of human cytochrome c oxidase, Gene, vol.55, pp.205-217, 1987.

J. Bereiter-hahn, M. Vöth, S. Mai, and M. Jendrach, Structural implications of mitochondrial dynamics, Biotechnology Journal, vol.135, issue.257
DOI : 10.1016/j.cub.2004.02.004

L. Lackner, Shaping the dynamic mitochondrial network, BMC Biology, vol.12, issue.1, pp.35-45, 2014.
DOI : 10.1523/JNEUROSCI.6248-09.2010

J. Hettinger, D. Richards, J. Hansson, M. Barra, A. Joschko et al., Origin of monocytes and macrophages in a committed progenitor, Nature Immunology, vol.172, issue.8, pp.821-830, 2013.
DOI : 10.1016/j.toxlet.2005.02.004

P. Murray and T. Wynn, Protective and pathogenic functions of macrophage subsets, Nature Reviews Immunology, vol.332, issue.11
DOI : 10.1126/science.1201475

A. Wheeler and A. Ridley, Why three Rho proteins? RhoA, RhoB, RhoC, and cell motility, Experimental Cell Research, vol.301, issue.1, pp.43-49, 2004.
DOI : 10.1016/j.yexcr.2004.08.012

T. Noguchi, M. Koizumi, and S. Hayashi, Mitochondria-driven cell elongation mechanism for competing sperms, Fly, vol.97, issue.2, pp.113-119, 2012.
DOI : 10.1534/genetics.111.131433
URL : http://www.tandfonline.com/doi/pdf/10.4161/fly.19862?needAccess=true

A. Pagliuso, P. Cossart, and . Stavru, The ever-growing complexity of the mitochondrial fission machinery, Cellular and Molecular Life Sciences, vol.28, issue.583???594
DOI : 10.1038/emboj.2009.89
URL : https://hal.archives-ouvertes.fr/pasteur-01574994

D. Suen, K. Norris, and R. Youle, Mitochondrial dynamics and apoptosis, Genes & Development, vol.22, issue.12, pp.1577-1590, 2008.
DOI : 10.1101/gad.1658508

S. Rafelski, Mitochondrial network morphology: building an integrative, geometrical view, BMC Biology, vol.11, issue.1, pp.71-78, 2013.
DOI : 10.1371/journal.pcbi.1002576
URL : https://bmcbiol.biomedcentral.com/track/pdf/10.1186/1741-7007-11-71?site=bmcbiol.biomedcentral.com

H. Hoitzing, I. Johnston, and N. Jones, What is the function of mitochondrial networks? A theoretical assessment of hypotheses and proposal for future research, BioEssays, vol.73, issue.6, pp.687-700, 2015.
DOI : 10.1158/0008-5472.CAN-13-1411

J. Friedman and J. Nunnari, Mitochondrial form and function, Nature, vol.108, issue.7483, pp.335-343, 2014.
DOI : 10.1073/pnas.1103295108

H. Chen, S. A. Detmer, A. J. Ewald, E. E. Griffin, S. E. Fraser et al., Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development, The Journal of Cell Biology, vol.114, issue.2, pp.189-200, 2003.
DOI : 10.1016/S1357-4310(98)01293-3
URL : http://jcb.rupress.org/content/jcb/160/2/189.full.pdf