, METHOD AND RESULTS OF THE PROJECT REFERENCES, vol.1

D. Wilde, R. Brölmann, H. Koninckx, P. Lundorff, P. Lower et al., Prevention of adhesions in gynaecological surgery: the 2012 European field guideline, Gynecological Surgery, vol.4, issue.5 Pt 1
DOI : 10.1046/j.1463-1318.2002.00374.x

, Gynecol Surg. 2012, vol.9, issue.4, pp.365-373

A. Miller, M. Hong, and J. Hutson, The broad ligament: A review of its anatomy and development in different species and hormonal environments, Clinical Anatomy, vol.49, issue.3, 2004.
DOI : 10.1016/S0090-4295(97)00104-0

S. Mutsaers, J. Baal, K. Van-de-vijver, R. Nieuwland, C. Van-noorden et al., The mesothelial cell, The International Journal of Biochemistry & Cell Biology, vol.36, issue.1, pp.9-16, 2004.
DOI : 10.1016/S1357-2725(03)00242-5

, Feb, vol.49, issue.1, pp.95-105

C. Lachaud, F. Soria, N. Escacena, E. Quesada-hernández, A. Hmadcha et al.,

, Mesothelial Cells: A Cellular Surrogate for Tissue Engineering of Corneal Endothelium Investig Opthalmology Vis Sci, p.5967, 2014.

A. Ferrandez-izquierdo, S. Navarro-fos, M. Gonzalez-devesa, and R. Gil-benso,

A. Bosch, Immunocytochemical typification of mesothelial cells in effusions: in vivo and in vitro models, Diagn Cytopathol, vol.10, issue.3, pp.256-62, 1994.

D. Paolo, N. Sacchi, G. , D. Vecchio, M. Nicolai et al., State of the Art on Autologous Mesothelial Transplant in Animals and Humans, The International Journal of Artificial Organs, vol.39, issue.3, 2007.
DOI : 10.1080/00365590410002492

C. Lachaud, J. López-beas, B. Soria, and A. Hmadcha, EGF-induced adipose tissue mesothelial cells undergo functional vascular smooth muscle differentiation. Cell Death Dis, p.1304, 2014.

A. Foley-comer, S. Herrick, T. Al-mishlab, C. Prêle, G. Laurent et al.,

, Evidence for incorporation of free-floating mesothelial cells as a mechanism of serosal healing, J Cell Sci, vol.115, pp.1383-1392, 2002.

S. Mutsaers, Mesothelial cells: their structure, function and role in serosal repair. Respirol Carlton Vic, pp.171-91, 2002.

, Available from: https://www.clinicalkey.fr, Mesothelial cells and peritoneal homeostasis- ClinicalKey [Internet]. [cited 2017, pp.1-2

S. Mutsaers, K. Birnie, S. Lansley, S. Herrick, C. Lim et al., Mesothelial cells in tissue repair and fibrosis. Front Pharmacol [Internet] Early demonstration of postoperative adhesions in a rodent model, Fertil Steril, vol.693, issue.8, pp.2734-2741, 2010.

A. Hirschelmann, G. Tchartchian, M. Wallwiener, A. Hackethal, D. Wilde et al., A review of the problematic adhesion prophylaxis in gynaecological surgery, Archives of Gynecology and Obstetrics, vol.161, issue.2, 2012.
DOI : 10.1016/j.jss.2008.11.839

M. Mavros, G. Velmahos, J. Lee, A. Larentzakis, and H. Kaafarani, Morbidity related to concomitant adhesions in abdominal surgery, Journal of Surgical Research, vol.192, issue.2, pp.286-92, 2014.
DOI : 10.1016/j.jss.2014.07.044

H. Ellis, The clinical significance of adhesions: focus on intestinal obstruction, Eur J Surg, issue.577, pp.5-9, 1997.

M. Parker, H. Ellis, B. Moran, J. Thompson, M. Wilson et al.,

, Postoperative adhesions: ten-year follow-up of 12,584 patients undergoing lower abdominal surgery, Dis Colon Rectum, vol.44, issue.6, pp.822-829, 2001.

R. Broek, Y. Issa, E. Van-santbrink, N. Bouvy, R. Kruitwagen et al., Burden of adhesions in abdominal and pelvic surgery: systematic review and met-analysis

, BMJ, vol.347, p.5588, 2013.

M. Ouaïssi, S. Gaujoux, N. Veyrie, E. Denève, C. Brigand et al., Post-operative adhesions after digestive surgery: Their incidence and prevention: Review of the literature, Journal of Visceral Surgery, vol.149, issue.2, pp.104-114
DOI : 10.1016/j.jviscsurg.2011.11.006

A. Lower, R. Hawthorn, D. Clark, J. Boyd, A. Finlayson et al., Adhesion-related readmissions following gynaecological laparoscopy or laparotomy in Scotland: an epidemiological study of 24 046 patients, Human Reproduction, vol.19, issue.8, pp.1877-85, 2004.
DOI : 10.1093/humrep/deh321

B. Monk, M. Berman, and F. Montz, Adhesions after extensive gynecologic surgery: Clinical significance, etiology, and prevention, American Journal of Obstetrics and Gynecology, vol.170, issue.5, pp.1396-403, 1994.
DOI : 10.1016/S0002-9378(13)90479-8

H. Ellis, B. Moran, J. Thompson, M. Parker, M. Wilson et al., Adhesion-related hospital readmissions after abdominal and pelvic surgery: a retrospective cohort study, The Lancet, vol.353, issue.9163, pp.1476-80, 1999.
DOI : 10.1016/S0140-6736(98)09337-4

H. Ellis, The Magnitude of Adhesion-Related Problems, Ann Chir Gynaecol, vol.87, issue.1, pp.9-11, 1998.
DOI : 10.1007/978-1-4612-1194-5_26

D. Swank, S. Swank-bordewijk, W. Hop, W. Van-erp, I. Janssen et al., Laparoscopic adhesiolysis in patients with chronic abdominal pain: a blinded randomised controlled multi-centre trial, The Lancet, vol.361, issue.9365, pp.1247-51, 2003.
DOI : 10.1016/S0140-6736(03)12979-0

A. Van-der-krabben, F. Dijkstra, M. Nieuwenhuijzen, M. Reijnen, M. Schaapveld et al., Morbidity and mortality of inadvertent enterotomy during adhesiotomy, British Journal of Surgery, vol.353, issue.4, pp.467-71, 2000.
DOI : 10.1016/S0140-6736(98)09337-4

M. Wilson, D. Menzies, A. Knight, and A. Crowe, Demonstrating the clinical and cost effectiveness of adhesion reduction strategies, Colorectal Disease, vol.222, issue.5, pp.355-60, 2002.
DOI : 10.1097/00000658-199508000-00003

G. Wei, X. Chen, G. Wang, L. Fan, K. Wang et al., Effect of Resveratrol on the Prevention of Intra-Abdominal Adhesion Formation in a Rat Model, Cellular Physiology and Biochemistry, vol.39, issue.1, pp.33-46, 2016.
DOI : 10.1159/000445603

Z. Bayhan, S. Zeren, F. Kocak, C. Kocak, R. Akc?lar et al., Antiadhesive and antiinflammatory effects of pirfenidone in postoperative intra-abdominal adhesion in an experimental rat model, J Surg Res. 2016, vol.201, issue.2, pp.348-55

S. Yan, Y. Yue, L. Zeng, J. Yue, W. Li et al., Effect of intra-abdominal administration of ligustrazine nanoparticles nano spray on postoperative peritoneal adhesion in rat model, Journal of Obstetrics and Gynaecology Research, vol.80, issue.12, 2015.
DOI : 10.1055/s-0034-1382877

F. Jamshidi-adegani, E. Seyedjafari, N. Gheibi, M. Soleimani, and M. Sahmani, Prevention of adhesion bands by ibuprofen-loaded PLGA nanofibers, Biotechnology Progress, vol.64, issue.4, 2016.
DOI : 10.1016/j.addr.2012.09.004

E. Topal, E. Ozturk, G. Sen, O. Yerci, and T. Yilmazlar, A Comparison of Three Fibrinolytic Agents in Prevention of Intra-Abdominal Adhesions, Acta Chirurgica Belgica, vol.110, issue.1, pp.71-76, 2010.
DOI : 10.1080/00015458.2010.11680569

Q. Xia, Z. Liu, C. Wang, Z. Zhang, S. Xu et al., A Biodegradable Trilayered Barrier Membrane Composed of Sponge and Electrospun Layers: Hemostasis and Antiadhesion, Biomacromolecules, vol.16, issue.9, pp.3083-92, 2015.
DOI : 10.1021/acs.biomac.5b01099

A. Hinoki, A. Saito, M. Kinoshita, J. Yamamoto, D. Saitoh et al., Polylactic acid nanosheets in prevention of postoperative intestinal adhesion and their effects on bacterial propagation in an experimental model, British Journal of Surgery, vol.165, issue.577, 2016.
DOI : 10.1097/00000658-196706000-00006

S. Bang, E. Lee, Y. Ko, W. Kim, and O. Kwon, Injectable pullulan hydrogel for the prevention of postoperative tissue adhesion, International Journal of Biological Macromolecules, vol.87, pp.155-62
DOI : 10.1016/j.ijbiomac.2016.02.026

L. Zhu and Y. Zhang, Postoperative anti-adhesion ability of a novel carboxymethyl chitosan from silkworm pupa in a rat cecal abrasion model, Materials Science and Engineering: C, vol.61, p.2016
DOI : 10.1016/j.msec.2015.12.080

S. Chiang, C. Cheng, K. Moulton, J. Kasznica, and S. Moulton, TNP-470 inhibits intraabdominal adhesion formation, Journal of Pediatric Surgery, vol.35, issue.2, pp.189-96, 2000.
DOI : 10.1016/S0022-3468(00)90008-3

A. Greene, I. Alwayn, V. Nose, E. Flynn, D. Sampson et al., Prevention of Intra-abdominal Adhesions Using the Antiangiogenic COX-2 Inhibitor Celecoxib, Annals of Surgery, vol.242, issue.1, pp.140-146, 2005.
DOI : 10.1097/01.sla.0000167847.53159.c1

J. Becker, M. Dayton, V. Fazio, D. Beck, S. Stryker et al., Prevention of postoperative abdominal adhesions by a sodium hyaluronate-based bioresorbable membrane: a prospective, randomized, double-blind multicenter study, J Am Coll Surg, 1996.

A. Dabrowski, M. Lepère, C. Zaranis, C. Coelio, and P. Hauters, Efficacy and safety of a resorbable collagen membrane COVA+??? for the prevention of postoperative adhesions in abdominal surgery, Surgical Endoscopy, vol.12, issue.2, pp.2358-66
DOI : 10.1089/109264202760268005

R. Brustia, O. Scatton, and O. Soubrane, Variation on a Theme: Alternative to Plastic Bag in ALPPS Procedures: Feasibility and Clinical Safety of COVA+??? Membrane in ALPPS Procedures, World Journal of Surgery, vol.258, issue.12, pp.3023-3030, 2015.
DOI : 10.1097/SLA.0b013e3182854949

K. Kawanishi, K. Nitta, M. Yamato, and T. Okano, Therapeutic Applications of Mesothelial Cell Sheets, Therapeutic Apheresis and Dialysis, vol.29, issue.Suppl 2, 2014.
DOI : 10.1093/ndt/gft397

J. Hwang, I. Kim, J. Lee, S. Piao, D. Lee et al., Therapeutic lymphangiogenesis using stem cell and VEGF-C hydrogel, Biomaterials, vol.32, issue.19, pp.4415-4438, 2011.
DOI : 10.1016/j.biomaterials.2011.02.051

Y. Kim, Y. Jun, J. Kim, and C. Kim, Effects of human adipose-derived stem cells on the regeneration of damaged visceral pleural mesothelial cells: a morphological study in a rabbit model, Interactive CardioVascular and Thoracic Surgery, vol.174, issue.3, pp.363-370, 2014.
DOI : 10.1164/rccm.200603-406OC

Y. Xu, R. Guan, H. Lei, H. Li, L. Wang et al., Therapeutic Potential of Adipose???Derived Stem Cells???Based Micro???Tissues in a Rat Model of Postprostatectomy Erectile Dysfunction, The Journal of Sexual Medicine, vol.11, issue.10, 2014.
DOI : 10.1111/jsm.12636

A. Boquest, A. Shahdadfar, K. Frønsdal, O. Sigurjonsson, S. Tunheim et al., Isolation and Transcription Profiling of Purified Uncultured Human Stromal Stem Cells: Alteration of Gene Expression after In Vitro Cell Culture, Molecular Biology of the Cell, vol.16, issue.3, pp.1131-1172, 2005.
DOI : 10.1089/107632701300062859

D. Rosa, A. , D. Francesco, F. Tirino, V. Ferraro et al., A New Method for Cryopreserving Adipose-Derived Stem Cells: An Attractive and Suitable Large-Scale and Long-Term Cell Banking Technology, Tissue Engineering Part C: Methods, vol.15, issue.4, pp.659-67, 2009.
DOI : 10.1089/ten.tec.2008.0674

D. Berry, D. Stenesen, D. Zeve, and J. Graff, The developmental origins of adipose tissue. Dev Camb Engl, pp.3939-3988, 2013.

F. Caserta, T. Tchkonia, V. Civelek, M. Prentki, N. Brown et al., Fat depot origin affects fatty acid handling in cultured rat and human preadipocytes, American Journal of Physiology-Endocrinology and Metabolism, vol.265, issue.2, pp.238-247, 2001.
DOI : 10.1074/jbc.273.12.6916

W. Tang, D. Zeve, J. Suh, D. Bosnakovski, M. Kyba et al., White Fat Progenitor Cells Reside in the Adipose Vasculature, Science, vol.56, issue.7, pp.583-589, 2008.
DOI : 10.1038/nm1611

N. Yamamoto, H. Akamatsu, S. Hasegawa, T. Yamada, S. Nakata et al., Isolation of multipotent stem cells from mouse adipose tissue, Journal of Dermatological Science, vol.48, issue.1, 2007.
DOI : 10.1016/j.jdermsci.2007.05.015

M. Rodeheffer, K. Birsoy, and J. Friedman, Identification of White Adipocyte Progenitor Cells In Vivo, Cell, vol.135, issue.2, pp.240-249, 2008.
DOI : 10.1016/j.cell.2008.09.036

P. Baer, Adipose-derived mesenchymal stromal/stem cells: An update on their phenotype in vivo and in vitro, World Journal of Stem Cells, vol.6, issue.3, p.256, 2014.
DOI : 10.1089/scd.2010.0355

P. Bertram, L. Tietze, M. Hoopmann, K. Treutner, C. Mittermayer et al.,

, Intraperitoneal transplantation of isologous mesothelial cells for prevention of adhesions

, Eur J Surg Acta Chir, vol.165, issue.7, pp.705-714, 1999.

P. Lucas, D. Warejcka, L. Zhang, W. Newman, and H. Young, Effect of Rat Mesenchymal Stem Cells on Development of Abdominal Adhesions after Surgery, Journal of Surgical Research, vol.62, issue.2, pp.229-232, 1996.
DOI : 10.1006/jsre.1996.0200

R. Kanda, C. Hamada, K. Kaneko, T. Nakano, K. Wakabayashi et al., Paracrine effects of transplanted mesothelial cells isolated from temperature-sensitive SV40 large Tantigen gene transgenic rats during peritoneal repair. Nephrol Dial Transplant Off Publ Eur Dial Transpl Assoc - Eur Ren Assoc, Feb, vol.29, issue.2, pp.289-300, 2014.

L. Hekking and J. Van-den-born, Feasibility of Mesothelial Transplantation during Experimental Peritoneal Dialysis and Peritonitis, The International Journal of Artificial Organs, vol.36, issue.2, pp.513-522, 2007.
DOI : 10.1016/j.biocel.2003.11.002

T. Asano, R. Takazawa, M. Yamato, R. Takagi, Y. Iimura et al., Transplantation of an Autologous Mesothelial Cell Sheet Prepared from Tunica Vaginalis Prevents Post-Operative Adhesions in a Canine Model, Tissue Engineering, vol.12, issue.9, pp.2629-2666, 2006.
DOI : 10.1089/ten.2006.12.2629

T. Asano, R. Takazawa, M. Yamato, K. Kihara, and T. Okano, Mesothelial Cells from Tunica Vaginalis, a Practical Source for Mesothelial Transplantation, The International Journal of Artificial Organs, vol.68, issue.3, 2007.
DOI : 10.1016/j.cardiores.2005.05.022

T. Asano, R. Takazawa, M. Yamato, Y. Kageyama, K. Kihara et al., Novel and simple method for isolating autologous mesothelial cells from the tunica vaginalis, BJU International, vol.115, issue.9, 2005.
DOI : 10.1007/978-1-4612-1194-5_1

M. Rodbell, . Localization, . Lipoprotein, . In, . Cells et al., J Biol Chem, vol.239, pp.753-758, 1964.

A. Hoffman, Hydrogels for biomedical applications, Adv Drug Deliv Rev, p.2012

M. Javaherzadeh, A. Shekarchizadeh, M. Kafaei, A. Mirafshrieh, N. Mosaffa et al., Effects of Intraperitoneal Administration of Simvastatin in Prevention of Postoperative Intraabdominal Adhesion Formation in Animal Model of Rat, Bull Emerg Trauma, 2016.

Z. Bayhan, S. Zeren, F. Kocak, C. Kocak, R. Akc?lar et al., Antiadhesive and antiinflammatory effects of pirfenidone in postoperative intra-abdominal adhesion in an experimental rat model, J Surg Res. 2016, vol.201, issue.2, pp.348-55

A. Sahbaz, O. Aynioglu, H. Isik, B. Gun, O. Cengil et al., Pycnogenol prevents peritoneal adhesions, Archives of Gynecology and Obstetrics, vol.28, issue.11, pp.1279-84, 2015.
DOI : 10.1002/ptr.5184

D. Allahverdi, T. Allahverdi, E. Yayla, S. Deprem, T. Merhan et al., Effects of alpha lipoic acid on intra-abdominal adhesion: an experimental study in a rat model, Turkish Journal of Trauma and Emergency Surgery, vol.21, issue.1, pp.9-14, 2015.
DOI : 10.5505/tjtes.2015.15985

M. Lee, C. Lee, H. Wang, T. Chou, M. Wu et al., Hypothermia Increases Tissue Plasminogen Activator Expression and Decreases Post-Operative Intra-Abdominal Adhesion, PLOS ONE, vol.44, issue.5, p.160627, 2016.
DOI : 10.1371/journal.pone.0160627.t002

D. Clercq, K. Schelfhout, C. Bracke, M. , D. Wever et al.,

, Genipin-crosslinked gelatin microspheres as a strategy to prevent postsurgical peritoneal adhesions: In vitro and in vivo characterization, Biomaterials. 2016, vol.96, pp.33-46

E. Bianchi, K. Boekelheide, M. Sigman, D. Lamb, S. Hall et al., Ghrelin Inhibits Post-Operative Adhesions via Blockage of the TGF-?? Signaling Pathway, PLOS ONE, vol.2006, issue.4, p.153968, 2016.
DOI : 10.1371/journal.pone.0153968.s002

G. Bove and S. Chapelle, Visceral mobilization can lyse and prevent peritoneal adhesions in a rat model, Journal of Bodywork and Movement Therapies, vol.16, issue.1, pp.76-82
DOI : 10.1016/j.jbmt.2011.02.004

S. Whang, J. Astudillo, E. Sporn, S. Bachman, B. Miedema et al., Search of the Best Peritoneal Adhesion Model: Comparison of Different Techniques in a Rat Model

, J Surg Res, vol.167, issue.2, pp.245-50, 2011.

W. Gaertner, G. Hagerman, I. Felemovicius, M. Bonsack, and J. Delaney, Two Experimental Models for Generating Abdominal Adhesions, J Surg Res, 2008.

C. Lauder, G. Garcea, A. Strickland, and G. Maddern, Use of a Modified Chitosan???Dextran Gel to Prevent Peritoneal Adhesions in a Rat Model, Journal of Surgical Research, vol.171, issue.2, pp.877-82, 2011.
DOI : 10.1016/j.jss.2010.06.028

K. Kawanishi, M. Yamato, R. Sakiyama, T. Okano, and K. Nitta, Peritoneal cell sheets composed of mesothelial cells and fibroblasts prevent intra-abdominal adhesion formation in a rat model, Journal of Tissue Engineering and Regenerative Medicine, vol.55, issue.10, p.110, 2013.
DOI : 10.1016/j.biomaterials.2005.04.061

M. Cassidy, A. Sherburne, S. Heydrick, and A. Stucchi, Combined intraoperative administration of a histone deacetylase inhibitor and a neurokinin-1 receptor antagonist synergistically reduces intra-abdominal adhesion formation in??a rat model, Surgery, vol.157, issue.3, 2015.
DOI : 10.1016/j.surg.2014.09.031

S. Sakai, K. Ueda, and M. Taya, Peritoneal adhesion prevention by a biodegradable hyaluronic acid-based hydrogel formed in situ through a cascade enzyme reaction initiated by contact with body fluid on tissue surfaces, Acta Biomaterialia, vol.24, pp.152-160
DOI : 10.1016/j.actbio.2015.06.023

M. Kutuk, M. Ozgun, C. Batukan, B. Ozcelik, M. Basbug et al., Oral tadalafil reduces intra-abdominal adhesion reformation in rats, Human Reproduction, vol.9, issue.4, p.2012
DOI : 10.1016/j.niox.2003.12.002

S. Tahmasebi, M. Tahamtan, and Y. Tahamtan, Prevention by rat amniotic fluid of adhesions after laparatomy in a rat model, International Journal of Surgery, vol.10, issue.1, pp.16-25, 2012.
DOI : 10.1016/j.ijsu.2011.11.003

C. Wallwiener, B. Kraemer, M. Wallwiener, C. Brochhausen, K. Isaacson et al., The extent of adhesion induction through electrocoagulation and suturing in an experimental rat study, Fertility and Sterility, vol.93, issue.4, pp.1040-1044, 2010.
DOI : 10.1016/j.fertnstert.2008.12.002

B. Kraemer, M. Scharpf, C. Planck, C. Tsaousidis, M. Enderle et al., Randomized experimental study to investigate the??peritoneal adhesion formation of??conventional monopolar contact coagulation versus noncontact argon plasma coagulation in a rat model, Fertility and Sterility, vol.102, issue.4, pp.1197-202, 2014.
DOI : 10.1016/j.fertnstert.2014.07.007

E. Agacayak, S. Tunc, M. Icen, U. Alabalik, F. Findik et al., Honokiol Decreases Intra-Abdominal Adhesion Formation in a Rat Model, Gynecologic and Obstetric Investigation, vol.79, issue.3, pp.160-167, 2015.
DOI : 10.1159/000367661

A. Karatas, T. Ozlu, G. Ozyalvacli, M. Tosun, A. Cetinkaya et al.,

, Intraperitoneal Nigella sativa for Prevention of Postoperative Intra-Abdominal Adhesions in Rats, J Invest Surg, vol.27, issue.6, pp.319-345, 2014.

H. Keskin, Y. Sirin, H. Keles, O. Turgut, T. Ide et al., The aromatase inhibitor letrozole reduces adhesion formation after intraperitoneal surgery in a rat uterine horn model, European Journal of Obstetrics & Gynecology and Reproductive Biology, vol.167, issue.2, pp.199-204
DOI : 10.1016/j.ejogrb.2012.12.002

S. Kelekci, B. Yilmaz, S. Oguz, S. Zergero?lu, I. Inan et al., The Efficacy of a Hyaluronate/Carboxymethylcellulose Membrane in Prevention of Postoperative Adhesion in a Rat Uterine Horn Model, The Tohoku Journal of Experimental Medicine, vol.204, issue.3, pp.189-94, 2004.
DOI : 10.1620/tjem.204.189

M. Oncel, F. Remzi, J. Connor, and V. Fazio, Comparison of cecal abrasion and multipleabrasion models in generating intra-abdominal adhesions for animal studies. Tech Coloproctology, pp.29-33, 2005.

, bipolar electrocoagulation [Internet]. TheFreeDictionary.com, 2017.

W. Link, F. Incropera, and J. Glover, Available from: http://medical-dictionary.thefreedictionary.com/bipolar+electrocoagulation 86 The plasma scalpel, Med Prog Technol, vol.4, issue.3, pp.123-154, 1976.

A. Foley-comer, S. Herrick, T. Al-mishlab, C. Prêle, G. Laurent et al.,

, Evidence for incorporation of free-floating mesothelial cells as a mechanism of serosal healing, J Cell Sci, vol.115, pp.1383-1392, 2002.

H. Ellis, The hazards of surgical glove dusting powders, Surg Gynecol Obstet, 1990.

D. Jagelman and H. Ellis, Starch and intraperitoneal adhesion formation, British Journal of Surgery, vol.16, issue.2, 1973.
DOI : 10.1001/jama.1943.02840500014005

, Feb, vol.60, issue.2, pp.111-115

M. Van-den-tol, R. Haverlag, M. Van-rossen, F. Bonthuis, R. Marquet et al., Glove powder promotes adhesion formation and facilitates tumour cell adhesion and growth, British Journal of Surgery, vol.31, issue.9, pp.1258-63, 2001.
DOI : 10.1159/000008639

O. Topcu, I. Kuzu, and K. Karayalcin, Effects of Peritoneal Lavage with Scolicidal Agents on Survival and Adhesion Formation in Rats, World Journal of Surgery, vol.389, issue.1, pp.127-160, 2006.
DOI : 10.1001/archsurg.1991.01410280122020

H. Laufman and T. Rubel, Synthetic absorable sutures, Surg Gynecol Obstet, 1977.

E. Chelala, H. Baraké, J. Estievenart, M. Dessily, F. Charara et al., Long-term outcomes of 1326 laparoscopic incisional and ventral hernia repair with the routine suturing concept: a single institution experience, Hernia, vol.237, issue.1, pp.101-111, 2016.
DOI : 10.1097/00000658-200301000-00018

A. Tandon, K. Shahzad, S. Pathak, C. Oommen, Q. Nunes et al., -IPOM for laparoscopic incisional and ventral hernia repair: a retrospective cohort study, The Annals of The Royal College of Surgeons of England, vol.98, issue.8, pp.568-73, 2016.
DOI : 10.1308/rcsann.2016.0292

M. Binda, C. Molinas, P. Hansen, and P. Koninckx, Effect of desiccation and temperature during laparoscopy on adhesion formation in mice, Fertility and Sterility, vol.86, issue.1, pp.166-75, 2006.
DOI : 10.1016/j.fertnstert.2005.11.079

N. Butz, S. Müller, K. Treutner, M. Anurov, S. Titkova et al., The influence of blood on the efficacy of intraperitoneally applied phospholipids for prevention of adhesions, BMC Surgery, vol.130, issue.1, p.14, 2007.
DOI : 10.1067/msy.2001.115102

D. Iaco, P. Muzzupapa, G. Bigon, E. Pressato, D. Donà et al., Efficacy of a hyaluronan derivative gel in postsurgical adhesion prevention in the presence of inadequate hemostasis, Surgery, vol.130, issue.1, pp.60-64, 2001.
DOI : 10.1067/msy.2001.115102

R. Leach, J. Burns, E. Dawe, M. Smithbarbour, and M. Diamond, Reduction of postsurgical adhesion formation in the rabbit uterine horn model with use of 112

, Fertil Steril, vol.69, issue.3, pp.415-423, 1998.

G. Saed, N. Fletcher, and M. Diamond, The Creation of a Model for Ex Vivo Development of Postoperative Adhesions, Reproductive Sciences, vol.10, issue.5, pp.610-612, 2016.
DOI : 10.1016/S0015-0282(98)00270-2

, Experience in Primary Culture of Human Peritoneal Mesothelial Cell, Chin J Physiol, 2012.

L. Aroeira, J. Loureiro, and G. González-mateo,

J. Tomero, Characterization of epithelial-to-mesenchymal transition of mesothelial cells in a mouse model of chronic peritoneal exposure to high glucose dialysate, Perit Dial Int J Int Soc Perit Dial, vol.28, issue.5, pp.29-33, 2008.

S. Katz, P. Balogh, N. Nagy, and A. Kiss, Epithelial-To-Mesenchymal Transition Induced by Freund???s Adjuvant Treatment in Rat Mesothelial Cells: A Morphological and Immunocytochemical Study, Pathology & Oncology Research, vol.276, issue.Suppl, pp.641-650
DOI : 10.1074/jbc.M100033200

A. Demir, P. Groothuis, A. Nap, C. Punyadeera, A. De-goeij et al., Menstrual effluent induces epithelial-mesenchymal transitions in mesothelial cells, Human Reproduction, vol.19, issue.1, pp.21-30, 2004.
DOI : 10.1093/humrep/deh042

M. Dhanasekaran, S. Indumathi, A. Kanmani, R. Poojitha, K. Revathy et al., Surface antigenic profiling of stem cells from human omentum fat in comparison with subcutaneous fat and bone marrow, Cytotechnology, vol.26, issue.5, pp.497-509, 2012.
DOI : 10.1002/cbf.1488

T. Iyyanki, L. Dunne, Q. Zhang, J. Hubenak, K. Turza et al., Adipose-Derived Stem-Cell-Seeded Non-Cross-Linked Porcine Acellular Dermal Matrix Increases Cellular Infiltration, Vascular Infiltration, and Mechanical Strength of Ventral Hernia Repairs, Tissue Engineering Part A, vol.21, issue.3-4, pp.3-4475, 2015.
DOI : 10.1089/ten.tea.2014.0235

G. Yu, X. Wu, G. Kilroy, Y. Halvorsen, J. Gimble et al., Isolation of Murine Adipose-Derived Stem Cells Available from, Adipose-Derived Stem Cells [Internet]. Totowa, pp.29-36978, 2011.

A. Ghorbani, S. Jalali, and M. Varedi, Isolation of adipose tissue mesenchymal stem cells without tissue destruction: A non-enzymatic method, Tissue and Cell, vol.46, issue.1, pp.54-62, 2014.
DOI : 10.1016/j.tice.2013.11.002

S. Colleoni, E. Bottani, I. Tessaro, G. Mari, B. Merlo et al., Isolation, growth and differentiation of equine mesenchymal stem cells: effect of donor, source, amount of tissue and supplementation with basic fibroblast growth factor, Veterinary Research Communications, vol.13, issue.8, 2009.
DOI : 10.1007/s11259-009-9229-0

C. Chavez-munoz, K. Nguyen, W. Xu, S. Hong, T. Mustoe et al., Transdifferentiation of Adipose-Derived Stem Cells into Keratinocyte-Like Cells: Engineering a Stratified Epidermis, PLoS ONE, vol.269, issue.12, p.80587, 2013.
DOI : 10.1371/journal.pone.0080587.t002

M. Zhang, M. Xu, Z. Zhou, K. Zhang, J. Zhou et al., The Differentiation of Human Adipose-Derived Stem Cells towards a Urothelium-Like Phenotype In Vitro and the Dynamic Temporal Changes of Related Cytokines by Both Paracrine and Autocrine Signal Regulation, PLoS ONE, vol.6, issue.4, p.95583, 2014.
DOI : 10.1371/journal.pone.0095583.s002

C. Wang, S. Yin, L. Cen, Q. Liu, W. Liu et al., Differentiation of Adipose-Derived Stem Cells into Contractile Smooth Muscle Cells Induced by Transforming Growth Factor-??1 and Bone Morphogenetic Protein-4, Tissue Engineering Part A, vol.16, issue.4, pp.1201-1214, 2010.
DOI : 10.1089/ten.tea.2009.0303

H. Kim, M. Mizuno, K. Furuhashi, T. Katsuno, T. Ozaki et al., Rat adipose tissue-derived stem cells attenuate peritoneal injuries in rat zymosan-induced peritonitis accompanied by complement activation, Cytotherapy, vol.16, issue.3, pp.357-68, 2014.
DOI : 10.1016/j.jcyt.2013.10.011

D. Ulrich, R. Muralitharan, and C. Gargett, Toward the use of endometrial and menstrual blood mesenchymal stem cells for cell-based therapies, Expert Opinion on Biological Therapy, vol.6, issue.1, 2013.
DOI : 10.1142/9789814289399_0022

A. Atala, F. Kasper, and A. Mikos, Engineering Complex Tissues, Science Translational Medicine, vol.7, issue.Suppl_6, pp.160-172, 2012.
DOI : 10.1098/rsif.2010.0348.focus

A. Asti and L. Gioglio, Natural and synthetic biodegradable polymers: different scaffolds for cell expansion and tissue formation, Int J Artif Organs, vol.37, issue.3, pp.187-205, 2014.

Z. Zou, Q. Zheng, Y. Wu, X. Guo, S. Yang et al., Biocompatibility and bioactivity of designer self-assembling nanofiber scaffold containing FGL motif for rat dorsal root ganglion neurons, Journal of Biomedical Materials Research Part A, vol.31, issue.4, pp.1125-1156, 2010.
DOI : 10.1002/jbm.a.31785

J. Guo, H. Su, Y. Zeng, Y. Liang, W. Wong et al., Reknitting the injured spinal cord by self-assembling peptide nanofiber scaffold, Nanomedicine: Nanotechnology, Biology and Medicine, vol.3, issue.4, pp.311-332, 2007.
DOI : 10.1016/j.nano.2007.09.003

A. Horii, X. Wang, F. Gelain, and S. Zhang, Biological Designer Self-Assembling Peptide Nanofiber Scaffolds Significantly Enhance Osteoblast Proliferation, Differentiation and 3-D Migration, PLoS ONE, vol.27, issue.2, p.190, 2007.
DOI : 10.1371/journal.pone.0000190.t002

URL : https://doi.org/10.1371/journal.pone.0000190

I. Dégano, L. Quintana, M. Vilalta, D. Horna, N. Rubio et al., The effect of self-assembling peptide nanofiber scaffolds on mouse embryonic fibroblast implantation and proliferation, Biomaterials, vol.30, issue.6, pp.1156-65, 2009.
DOI : 10.1016/j.biomaterials.2008.11.021

H. Song, L. Zhang, and X. Zhao, Hemostatic Efficacy of Biological Self-Assembling Peptide Nanofibers in a Rat Kidney Model, Macromolecular Bioscience, vol.8, issue.1, pp.33-42, 2010.
DOI : 10.1016/S0039-6060(99)70092-9

B. Cavalcanti, B. Zeitlin, and J. Nör, A hydrogel scaffold that maintains viability and supports differentiation of dental pulp stem cells, Dental Materials, vol.29, issue.1, pp.97-102, 2013.
DOI : 10.1016/j.dental.2012.08.002

W. Dissanayaka, K. Hargreaves, J. L. Samaranayake, L. Zhang, and C. , The interplay of dental pulp stem cells and endothelial cells in an injectable peptide hydrogel on angiogenesis and pulp regeneration in vivo, Tissue Eng Part A. Feb, vol.21, pp.3-4550, 2015.

H. Aligholi, S. Rezayat, H. Azari, E. Mehr, S. Akbari et al., Preparing neural stem/progenitor cells in PuraMatrix hydrogel for transplantation after brain injury in rats: A comparative methodological study, Brain Research, vol.1642, pp.197-208, 2016.
DOI : 10.1016/j.brainres.2016.03.043

F. Moradi, M. Bahktiari, M. Joghataei, M. Nobakht, M. Soleimani et al.,

, BD PuraMatrix peptide hydrogel as a culture system for human fetal Schwann cells in spinal cord regeneration, J Neurosci Res. 2012, vol.90, issue.12, pp.2335-2383

M. Tokunaga, M. Liu, T. Nagai, K. Iwanaga, K. Matsuura et al.,

, Implantation of cardiac progenitor cells using self-assembling peptide improves cardiac function after myocardial infarction, J Mol Cell Cardiol, vol.49, issue.6, pp.972-83, 2010.

H. Guo, G. Cui, H. Wang, and Y. Tan, Transplantation of marrow-derived cardiac stem cells carried in designer self-assembling peptide nanofibers improves cardiac function after myocardial infarction, Biochemical and Biophysical Research Communications, vol.399, issue.1, pp.42-50, 2010.
DOI : 10.1016/j.bbrc.2010.07.031

N. Akiyama, T. Yamamoto-fukuda, H. Takahashi, and T. Koji, In situ tissue engineering with synthetic self-assembling peptide nanofiber scaffolds, PuraMatrix, for mucosal regeneration in the rat middle-ear, International Journal of Nanomedicine, vol.8, pp.2629-2669, 2013.
DOI : 10.2147/IJN.S47279

C. Mason and P. Dunnill, A brief definition of regenerative medicine, Regenerative Medicine, vol.2, issue.1, 2008.
DOI : 10.1186/1471-2202-8-36

J. Fraser, K. Hicok, R. Shanahan, M. Zhu, S. Miller et al., System: Automated Processing of Adipose-Derived Regenerative Cells in a Functionally Closed System, Advances in Wound Care, vol.3, issue.1, pp.38-45, 2014.
DOI : 10.1089/wound.2012.0408

Q. Denost, Ing?enierie tissulaire en chirurgie colorectale : du d?efect pari?etal au remplace- ment d'organe : ?etude in vitro et in vivo, pp.2014-0188, 2014.

J. Lehmann, R. Schulz, and R. Sanzenbacher, Strategic considerations on the design and choice of animal models for non-clinical investigations of cell-based medicinal products], Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz, vol.58, pp.11-121215, 2015.

T. Bubela and C. Mccabe, Value-Engineered Translation for Regenerative Medicine: Meeting the Needs of Health Systems, Stem Cells and Development, vol.22, issue.S1, pp.89-93, 2013.
DOI : 10.1089/scd.2013.0398

M. Corbett, A. Webster, R. Hawkins, and N. Woolacott, Innovative regenerative medicines in the EU: a better future in evidence?, BMC Medicine, vol.1, issue.1, p.49, 2017.
DOI : 10.5966/sctm.2011-0009