P. S. Zammit, Function of the myogenic regulatory factors Myf5, MyoD, Myogenin and MRF4 in skeletal muscle, satellite cells and regenerative myogenesis, Semin Cell Dev Biol, vol.72, pp.19-32, 2017.

V. Horsley and G. K. Pavlath, Forming a multinucleated cell: molecules that regulate myoblast fusion, Cells Tissues Organs, vol.176, pp.67-78, 2004.

L. A. Moyle, F. S. Tedesco, and S. Benedetti, Pericytes in muscular dystrophies, Advances in experimental medicine and biology, pp.319-363, 2019.

M. Rai, U. Nongthomba, and M. D. Grounds, Skeletal muscle degeneration and regeneration in mice and flies, Curr Top Dev Biol, vol.108, pp.247-81, 2014.

T. Sugiyama, H. Kohara, M. Noda, and T. Nagasawa, Maintenance of the hematopoietic stem cell pool by CXCL12-CXCR4 chemokine signaling in bone marrow stromal cell niches, Immunity, vol.25, pp.977-88, 2006.

M. Z. Ratajczak, E. Zuba-surma, M. Kucia, R. Reca, W. Wojakowski et al., The pleiotropic effects of the SDF-1-CXCR4 axis in organogenesis, regeneration and tumorigenesis, Leukemia, vol.20, pp.1915-1939, 2006.

Y. Monneau, F. Arenzana-seisdedos, L. , and H. , The sweet spot: how GAGs help chemokines guide migrating cells, J Leukoc Biol, vol.99, pp.935-53, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01352726

I. Petit, D. Jin, and S. Rafii, The SDF-1-CXCR4 signaling pathway: a molecular hub modulating neo-angiogenesis, Trends Immunol, vol.28, pp.299-307, 2007.

K. Hiasa, M. Ishibashi, K. Ohtani, S. Inoue, Q. Zhao et al., Gene transfer of stromal cell-derived factor-1alpha enhances ischemic vasculogenesis and angiogenesis via vascular endothelial growth factor/endothelial nitric oxide synthase-related pathway: next-generation chemokine therapy for therapeutic neovasculariz, Circulation, vol.109, pp.2454-61, 2004.

N. Unoki, T. Murakami, K. Nishijima, K. Ogino, N. Van-rooijen et al., SDF-1/CXCR4 contributes to the activation of tip cells and microglia in retinal angiogenesis, Investig Ophthalmol Vis Sci, vol.51, pp.3362-71, 2010.

L. Wang, S. Guo, N. Zhang, Y. Tao, H. Zhang et al., The role of SDF-1/CXCR4 in the vasculogenesis and remodeling of cerebral arteriovenous malformation, Ther Clin Risk Manag, vol.11, pp.1337-1381, 2015.

E. De-falco, D. Porcelli, A. R. Torella, S. Straino, M. G. Iachininoto et al., SDF-1 involvement in endothelial phenotype and ischemia-induced recruitment of bone marrow progenitor cells, Blood, vol.104, pp.3472-82, 2004.

M. Bobadilla, N. Sainz, G. Abizanda, J. Orbe, J. A. Rodriguez et al., The CXCR4/SDF1 axis improves muscle regeneration through MMP-10 activity, Stem Cells Dev, vol.23, pp.1417-1444, 2014.

P. Rueda, A. Richart, A. Récalde, P. Gasse, J. Vilar et al., Homeostatic and tissue reparation defaults in mice carrying selective genetic invalidation of CXCL12/ proteoglycan interactions, Circulation, vol.126, pp.1882-95, 2012.
URL : https://hal.archives-ouvertes.fr/pasteur-00743099

C. Latroche, M. Weiss-gayet, L. Muller, C. Gitiaux, P. Leblanc et al., Coupling between myogenesis and angiogenesis during skeletal muscle regeneration is stimulated by restorative macrophages, Stem Cell Reports, vol.9, pp.2018-2051, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01800314

D. E. Sims, The pericyte-a review, Tissue Cell, vol.18, pp.153-74, 1986.

M. Ema, S. Takahashi, and J. Rossant, Deletion of the selection cassette, but not cis-acting elements, in targeted Flk1-lacZ allele reveals Flk1 expression in multipotent mesodermal progenitors, Blood, vol.107, pp.111-118, 2006.

R. Sambasivan, B. Gayraud-morel, G. Dumas, C. Cimper, S. Paisant et al., Distinct regulatory cascades govern extraocular and pharyngeal arch muscle progenitor cell fates, Dev Cell, vol.16, pp.810-831, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00428975

D. Hardy, A. Besnard, M. Latil, G. Jouvion, D. Briand et al., Comparative study of injury models for studying muscle regeneration in mice, PLoS One, vol.11, p.147198, 2016.
URL : https://hal.archives-ouvertes.fr/pasteur-01447903

J. C. Casar, C. Cabello-verrugio, H. Olguin, R. Aldunate, N. C. Inestrosa et al., Heparan sulfate proteoglycans are increased during skeletal muscle regeneration: requirement of syndecan-3 for successful fiber formation, J Cell Sci, vol.117, pp.73-84, 2004.

A. Q. Phan, J. Lee, M. Oei, C. Flath, C. Hwe et al., Positional information in axolotl and mouse limb extracellular matrix is mediated via heparan sulfate and fibroblast growth factor during limb regeneration in the axolotl (Ambystoma mexicanum), Regeneration, vol.2, pp.182-201, 2015.

P. Rueda, K. Balabanian, B. Lagane, I. Staropoli, K. Chow et al., The CXCL12? chemokine displays unprecedented structural and functional properties that make it a paradigm of chemoattractant proteins, PLoS One, vol.3, p.2543, 2008.
URL : https://hal.archives-ouvertes.fr/pasteur-00315593

B. J. Connell, R. Sadir, F. Baleux, C. Laguri, J. Kleman et al., Heparan sulfate differentially controls CXCL12 -and CXCL12 -mediated cell migration through differential presentation to their receptor CXCR4, Sci Signal, vol.9, p.107, 2016.

E. Brzoska, M. Kowalewska, A. Markowska-zagrajek, K. Kowalski, K. Archacka et al., Sdf-1 (CXCL12) improves skeletal muscle regeneration via the mobilisation of Cxcr4 and CD34 expressing cells, Biol. Cell, vol.104, pp.722-759, 2012.

G. B. Martinelli, D. Olivari, R. Cecconi, A. D. Talamini, L. Ottoboni et al., Activation of the SDF1/CXCR4 pathway retards muscle atrophy during cancer cachexia, Oncogene, vol.35, pp.6212-6234, 2016.

C. A. Griffin, L. H. Apponi, K. K. Long, and G. K. Pavlath, Chemokine expression and control of muscle cell migration during myogenesis, J Cell Sci, vol.123, pp.3052-60, 2010.

F. Dalonneau, X. Q. Liu, R. Sadir, J. Almodovar, H. C. Mertani et al., The effect of delivering the chemokine SDF-1? in a matrix-bound manner on myogenesis, Biomaterials, vol.35, pp.4525-4560, 2014.
URL : https://hal.archives-ouvertes.fr/hal-01053349

C. Christov, F. Chrétien, R. Abou-khalil, G. Bassez, G. Vallet et al., Muscle satellite cells and endothelial cells: close neighbors and privileged partners, Mol Biol Cell, vol.18, pp.1397-409, 2007.
URL : https://hal.archives-ouvertes.fr/inserm-00128985

M. Verma, Y. Asakura, B. Murakonda, T. Pengo, C. Latroche et al., Muscle satellite cell cross-talk with a vascular niche maintains quiescence via VEGF and notch signaling, Cell Stem Cell, vol.23, pp.530-543, 2018.

G. O'boyle, P. Mellor, J. A. Kirby, and S. Ali, Anti-inflammatory therapy by intravenous delivery of non-heparan sulfate-binding CXCL12, FASEB J, vol.23, pp.3906-3922, 2009.

M. Grunewald, A. I. Dor, Y. Bachar-lustig, E. Itin, A. Jung et al., VEGF-induced adult neovascularization: recruitment, retention, and role of accessory cells, Cell, vol.124, pp.175-89, 2006.

A. Zernecke, A. Schober, I. Bot, P. Von-hundelshausen, E. A. Liehn et al., SDF-1alpha/CXCR4 axis is instrumental in neointimal hyperplasia and recruitment of smooth muscle progenitor cells, Circ Res, vol.96, pp.784-91, 2005.

G. E. Davis, P. R. Norden, and S. Bowers, Molecular control of capillary morphogenesis and maturation by recognition and remodeling of the extracellular matrix: functional roles of endothelial cells and pericytes in health and disease, Connect Tissue Res, vol.2015, pp.1-11

S. Lin, T. Kisseleva, D. A. Brenner, and J. S. Duffield, Pericytes and perivascular fibroblasts are the primary source of collagen-producing cells in obstructive fibrosis of the kidney, Am J Pathol, vol.173, pp.1617-1644, 2008.

S. Lin, C. Schrimpf, C. Chen, Y. Wu, C. Wu et al., Targeting endothelium-pericyte cross talk by inhibiting VEGF receptor signaling attenuates kidney microvascular rarefaction and fibrosis, Am J Pathol, vol.178, pp.911-934, 2011.

E. K. Jackson, Y. Zhang, D. D. Gillespie, X. Zhu, D. Cheng et al., SDF-1? (stromal cell-derived factor 1?) induces cardiac fibroblasts, renal microvascular smooth muscle cells, and glomerular mesangial cells to proliferate, cause hypertrophy, and produce collagen, J Am Heart Assoc, vol.6, 2017.

F. Verkaar, J. Van-offenbeek, M. Van-der-lee, L. Van-lith, A. O. Watts et al., Chemokine cooperativity is caused by competitive glycosaminoglycan binding, J Immunol, vol.192, pp.3908-3922, 2014.

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