Rapid Protocol of Porcine Kidney Decellularization

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Abstract:

Chronic kidney disease is a problem that has grown in recent decades worldwide. The National Kidney Foundation (NKF) estimates that the number of patients will double in the next 10 years. Dialysis and kidney transplantation are the treatments used for chronic kidney disease. There is hope in slowing down chronic kidney disease or even stopping its progression. Bioengineering and cell therapy are the main fields in kidney regeneration research using three-dimensional matrices in which cells are cultured, an ideal solution for scarcity organs for kidney transplantation. The difficulty in re-creating a functional kidney due to the complexity of its three-dimensional structure and its composition of different cell types and that can be incorporated in vivo with low immunogenicity is a very difficult task. Therefore, the aim of the present study was to meet the enormous demand for new treatments, developing strategies of tissue engineering on the basis of the decellularization of the porcine kidney performed through a new cell removal protocol. We determined the effective removal of cells by histologic and immunohistochemical analyses, showing the preservation of type IV collagen and fibronectin. Therefore, this method is a quick way to obtain decellularized porcine kidneys for future recellularization studies.

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[1] Coresh J, Byrd-Holt D, Astor BC, Briggs JP, Eggers P W, Lacher DA, et al. Chronic kidney disease awareness, prevalence and trends among U.S. adults, 1999 to 2000. J Am Soc Nephrol. 16(1):180-8 (2005).

DOI: 10.1681/asn.2004070539

Google Scholar

[2] Mezzano S, Aros C. Chronic kidney disease: classification, mechanisms of progression and strategies for renoprotection. Rev Med Chil. 133(3):338-48 (2005) Spanish.

Google Scholar

[3] United States Renal Data System. 2013 USRDS annual data report: atlas of chronic kidney disease and end-stage renal disease in the United States. Am J Kidney Dis. 63(1 Suppl):e1-e478 (2014).

DOI: 10.1053/s0272-6386(05)01820-2

Google Scholar

[4] Information on https://www.theisn.org/initiatives/ckd - International Society of Nephrology [Internet]. Brussels; c2017 [cited 2017 Jul 11].

Google Scholar

[5] KDOQI; National Kidney Foundation. KDOQI clinical practice guidelines and clinical practice recommendations for anemia in chronic kidney disease. Am J Kidney Dis. 47(5 Suppl 3):S11-145 (2006).

DOI: 10.1053/j.ajkd.2006.12.005

Google Scholar

[6] Maeshima A, Nakasatomi M, Nojima Y. Regenerative medicine for the kidney: renotropic factors, renal stem/progenitor cells and stem cell therapy. Biomed Res Int. 595493 (2014).

DOI: 10.1155/2014/595493

Google Scholar

[7] Pino CJ, Humes HD. Stem cell technology for the treatment of acute and chonic renal failure. Transl Res. 156(3):161-8 (2010).

Google Scholar

[8] Fissell WH, Fleischman AJ, Humes HD, Roy S. Development of continuous ilantable renal replacement: past and future. Transl Res. 150(6):327-36 (2007).

DOI: 10.1016/j.trsl.2007.06.001

Google Scholar

[9] Montserrat N, Garreta E, Izpisua Belmonte JC. Regenerative strategies for kidney engineering. FEBS. 283(18):3303-24 (2016).

DOI: 10.1111/febs.13704

Google Scholar

[10] Tapias LF, Ott HC. Decellularized scaffolds as a platform for bioengineered organs. Curr Opin Organ Transplant. 19(2):145-52 (2014).

DOI: 10.1097/mot.0000000000000051

Google Scholar

[11] Crapo PM, Gilbert TW, Badylak SF. An overview of tissue and whole organ decellularization processes. Biomaterials. 32(12):3233-43 (2011).

DOI: 10.1016/j.biomaterials.2011.01.057

Google Scholar

[12] He M, Callanan A. Comparison of methods for whole-organ decellularization in tissue engineering of bioartificial organs. Tissue Eng Part B Rev. 19(3):194-208 (2013).

DOI: 10.1089/ten.teb.2012.0340

Google Scholar

[13] Keane TJ, Swinehart I, Badylak SF. Methods of tissue decellularization used for preparation of biologic scaffolds and in-vivo relevance. Methods. 84:25-34 (2015).

DOI: 10.1016/j.ymeth.2015.03.005

Google Scholar

[14] Nakayama KH, Lee CC, Batchelder CA, Tarantal AF. Tissue specificity of decellularized rhesus monkey kidney and lung scaffolds. PLoS One. 8(5):e64134 (2013).

DOI: 10.1371/journal.pone.0064134

Google Scholar

[15] Patient mortality and survival. United States Renal Data System. Am J Kidney Dis. 32(2 Suppl 1):S69-80 (1998).

Google Scholar

[16] Humes HD, Szczypka MS. Advances in cell therapy for renal failure. Transpl. Immunol. 12(3-4):219-27 (2004).

Google Scholar

[17] Ott HC, Matthiesen TS, Goh SK, Black LD, Kren SM, Netoff TI, et al. Perfusion-decellularized matrix: using nature's plataform to engineer a bioartificial heart. Nat Med. 14(2):213-21 (2008).

DOI: 10.1038/nm1684

Google Scholar

[18] Baptista PM, Siddiqui MM, Lozier G, Rodriguez SR, Atala A, Soker S. The use of whole organ decellularization for the generation of a vascularized liver organoid. Hepatology. 53(2):604-17 (2011).

DOI: 10.1002/hep.24067

Google Scholar

[19] Ott HC, Clippinger B, Conrad C, Schuetz C, Pomerantseva I, Ikonomou L, et al. Regeneration and orthotopic transplantation of a bioartificial lung. Nat Med. 16(8):927-31 (2010).

DOI: 10.1038/nm.2193

Google Scholar

[20] Ross EA, Williams MJ, Hamazaki T, Terada N, Clapp WL, Adin C, et al. Embryonic stem cells proliferate and differentiate when seeded into kidney scalffolds. J Am Soc Nephrol. 20(11):2338-47 (2009).

DOI: 10.1681/asn.2008111196

Google Scholar

[21] Bonandrini B, Figliuzzi M, Papadimou E, Morigi M, Perico N, Casiraghi F, et al. Recellularization of well-preserved acellular kidney scaffold using embryonic stem cells. Tissue Eng Part A. 20(9-10):1486-98 (2017).

DOI: 10.1089/ten.tea.2013.0269

Google Scholar

[22] Song JJ, Guyette JP, Gilpin SE, Gonzalez G, Vacanti JP, Otto HC. Regeneration and experimental orthotopic transplantation of a bioengineered kidey. Nat Med. 19(5):646-51 (2013).

DOI: 10.1038/nm.3154

Google Scholar

[23] Wang Y, Bao J, Wu Q, Zhou Y, Li Y, Wu X, et al. Method for perfusion decellularization of porcine whole liver and kidney for use as a scaffold for clinical-scale bioengineering engrafts. Xenotransplantation. 22(1):48-61 (2015).

DOI: 10.1111/xen.12141

Google Scholar

[24] Kim SS, Sundback CA, Kaihara S, Benvenuto MS, Kim BS, Mooney DJ, et al. Dynamic seeding and in vitro culture of hepatocytes in a flow perfusion system. Tissue Eng. 6(1):39-44 (2000).

DOI: 10.1089/107632700320874

Google Scholar

[25] Westover AJ, Buffington DA, Humes HD. Enhanced propagation of adult renal epithelial progenitor cells to improve cell sourcing for tissue engineered therapeutic devices for renal diseases. J Tissue Eng Regen Med. 6(8):589-97 (2012).

DOI: 10.1002/term.471

Google Scholar

[26] Smith PL, Buffington DA, Humes HD. Kidney epithelial cells. Methods Enzymol. 419:194-207 (2006).

Google Scholar