Research article Special Issues

Patient use of autologous cryopreserved intact adipose tissue from lipoaspirate

  • Autologous fat grafting has now been extensively and successfully performed for more than two decades. Although most adipose grafts and adipose-derived MSC therapies are done with fresh tissue, cryopreservation of tissue allows much greater flexibility of use. Over the course of five years, 194 cryopreserved adipose samples were thawed and returned to the collecting physician for subsequent autologous applications. Samples were stored with a mean cryogenic storage time of 9.5 months with some samples being stored as long as 44 months. The volumes of tissue stored varied from 12 cc to as large as 960 cc. Upon thaw the volume of recovered whole adipose tissue averaged 67% of the original amount stored. The recovery ranged from a low of 21% (n = 1) to a high of 100% (n = 1). Recovery was not found to be a function of collection volume, amount of tissue thawed, or length of time in cryopreservation. No association was found between tissue recovery and patient age. Viability of thawed cells remained high with a mean value of 91%. While an average recovery of 67% of volume frozen indicates that the use of banked and thawed tissue requires a larger amount of sample be taken from the patient initially, this requirement is easily accomplished by an experienced clinician. As cryopreservation of adipose tissue becomes more commonplace physicians will find it helpful to know the amount and quality of tissue that will be available after thawing procedures.

    Citation: Michael S. Badowski, Angela Muise, David T. Harris. Patient use of autologous cryopreserved intact adipose tissue from lipoaspirate[J]. AIMS Cell and Tissue Engineering, 2017, 1(3): 224-235. doi: 10.3934/celltissue.2017.3.224

    Related Papers:

  • Autologous fat grafting has now been extensively and successfully performed for more than two decades. Although most adipose grafts and adipose-derived MSC therapies are done with fresh tissue, cryopreservation of tissue allows much greater flexibility of use. Over the course of five years, 194 cryopreserved adipose samples were thawed and returned to the collecting physician for subsequent autologous applications. Samples were stored with a mean cryogenic storage time of 9.5 months with some samples being stored as long as 44 months. The volumes of tissue stored varied from 12 cc to as large as 960 cc. Upon thaw the volume of recovered whole adipose tissue averaged 67% of the original amount stored. The recovery ranged from a low of 21% (n = 1) to a high of 100% (n = 1). Recovery was not found to be a function of collection volume, amount of tissue thawed, or length of time in cryopreservation. No association was found between tissue recovery and patient age. Viability of thawed cells remained high with a mean value of 91%. While an average recovery of 67% of volume frozen indicates that the use of banked and thawed tissue requires a larger amount of sample be taken from the patient initially, this requirement is easily accomplished by an experienced clinician. As cryopreservation of adipose tissue becomes more commonplace physicians will find it helpful to know the amount and quality of tissue that will be available after thawing procedures.


    加载中
    [1] Neuber G (1983) Uber die Wiederanheilung vollstandig vom Korper getrennter, die ganze Fettschicht enthaltender Hautstucke. Zbl f Chir 30: 16–17.
    [2] Peer LA (1955) Transplantation of Tissues. Williams & Wilkins.
    [3] Illouz YG (1986) The fat cell "graft": a new technique to fill depressions. Plast Reconstr Surg 78: 122–123. doi: 10.1097/00006534-198607000-00028
    [4] Fournier PF (1985) Microlipoextraction et microlipoinjection. Rev Cir Esthet Langue 10: 36–40.
    [5] Coleman S (1995) Long-term survival of fat transplants: Controlled demonstrations. Aesthetic Plast Surg 19: 421–425. doi: 10.1007/BF00453875
    [6] Pu LL, Cui X, Fink BF, et al. (2004) Long-term preservation of adipose aspirates after conventional lipoplasty. Aesthet Surg J 24: 536–541. doi: 10.1016/j.asj.2004.09.002
    [7] Shu Z, Gao D, Pu LL (2015) Update on cryopreservation of adipose tissue and adipose-derived stem cells. Clin Plast Surg 42: 209–218. doi: 10.1016/j.cps.2014.12.001
    [8] Marten T, Elyassnia D (2015) Fat grafting in facial rejuvenation. Clin Plast Surg 42: 219–252. doi: 10.1016/j.cps.2014.12.003
    [9] Bircoll M (1987) Cosmetic breast augmentation using autologous fat and liposuction techniques. Plast Reconstr Surg 79: 267–271. doi: 10.1097/00006534-198702000-00022
    [10] Wakabayashi K, Hamada C, Kanda R, et al. (2014) Adipose-derived mesenchymal stem cells transplantation facilitate experimental peritoneal fibrosis repair by suppressing epithelial-mesenchymal transition. J Nephrol 27: 507–514. doi: 10.1007/s40620-014-0133-5
    [11] Bai X, Alt E (2010) Myocardial regeneration potential of adipose tissue-derived stem cells. Biochem Biophys Res Commun 401: 321–326. doi: 10.1016/j.bbrc.2010.09.012
    [12] Yang YC, Liu BS, Shen CC, et al. (2011) Transplantation of adipose tissue-derived stem cells for treatment of focal cerebral ischemia. Curr Neurovasc Res 8: 1–13. doi: 10.2174/156720211794520215
    [13] Ohnishi S, Ohgushi H, Kitamura S, et al. (2007) Mesenchymal stem cells for the treatment of heart failure. Intl J Hematol 86: 17–21. doi: 10.1532/IJH97.07041
    [14] Ii M, Horii M, Yokoyama A, et al. (2011) Synergistic effect of adipose-derived stem cell therapy and bone marrow progenitor recruitment in ischemic heart. Lab Invest 91: 539–552. doi: 10.1038/labinvest.2010.191
    [15] Dave SD, Vanikar AV, Trivedi HL (2013) Extrinsic factors promoting in vitro differentiation of insulin-secreting cells from human adipose tissue-derived mesenchymal stem cells. Appl Biochem Biotechnol 170: 962–971. doi: 10.1007/s12010-013-0250-y
    [16] Timper K, Seboek D, Eberhardt M, et al. (2006) Human adipose tissue-derived mesenchymal stem cells differentiate into insulin, somatostatin, and glucagon expressing cells. Biochem Biophys Res Commun 341: 1135–1140. doi: 10.1016/j.bbrc.2006.01.072
    [17] McKinney P, Pandya S (1994) Use of pubic fat as a graft for eyelid defects. Aesthetic Plast Surg 18: 383–385. doi: 10.1007/BF00451344
    [18] Li TS, Choong MY, Wu CI, et al. (2011) Autologous fat graft to restore nail bed contour following resection of a subungual glomus. J Hand Surg Am 36: 726–728.
    [19] Agostini T, Perello R (2015) Lipomodeling: An Innovative Approach to Global Volumetric Rejuvenation of the Hand. Aesthet Surg J 35: 708–714. doi: 10.1093/asj/sju163
    [20] Kiviluoto O (1976) Use of free fat transplants to prevent epidural scar formation. An experimental study. Acta Orthop Scand Suppl 164: 3–75.
    [21] Klinger M, Caviggioli F, Klinger FM, et al. (2013) Autologous fat graft in scar treatment. J Craniofac Surg 24: 1610–1615. doi: 10.1097/SCS.0b013e3182a24548
    [22] Shakhov AA (2002) Fat transplantation and breast augmentation. Aestetic Plast Surg 26: 323–325. doi: 10.1007/s00266-002-2032-8
    [23] Parrish JN, Metzinger SE (2010) Autogenous fat grafting and breast augmentation: a review of the literature. Aesthet Surg J 30: 549–556. doi: 10.1177/1090820X10380859
    [24] Carraway JH, Mellow CG (1990) Syringe aspiration and fat concentration: a simple technique for autologous fat injection. Ann Plast Surg 24: 293–296. doi: 10.1097/00000637-199003000-00018
    [25] Choi JW, Kim SC, Park EJ, et al. (2018) Positive Effect of Incubated Adipose-Derived Mesenchymal Stem Cells on Microfat Graft Survival. J Craniofac Surg 29: 243–247.
    [26] Tonnard P, Verpaele A, Peeters G, et al. (2013) Nanofat grafting: basic research and clinical applications. Plast Reconstr Surg 132: 1017–1026. doi: 10.1097/PRS.0b013e31829fe1b0
    [27] Stuzin JM (2013) Discussion: Nanofat grafting: basic research and clinical applications. Plast Reconstr Surg 132: 1027–1028. doi: 10.1097/PRS.0b013e31829fe246
    [28] Choudhery MS, Badowski MS, Muise A, et al. (2014) Cryopreservation of whole adipose tissue for future use in regenerative medicine. J Surg Res 187: 24–35. doi: 10.1016/j.jss.2013.09.027
    [29] Choudhery MS, Badowski MS, Muise A, et al. (2014) Donor age negatively impacts adipose tissue-derived mesenchymal stem cell expansion and differentiation. J Transl Med 12: 8. doi: 10.1186/1479-5876-12-8
    [30] Zuk PA, Zhu M, Mizuno H, et al. (2001) Multilineage cells from human adipose tissue: implications for cell-based therapies. Tissue Eng 7: 211–228. doi: 10.1089/107632701300062859
    [31] Lowenstein J, Floridia R, Rosolia H (1964) Preservation of bone marrow and blood at cryogenic temperatures. J Cardiovasc Surg 5: 313–326.
    [32] Armitage S, Warwick R, Fehily D, et al. (1999) Cord blood banking in London: the first 1000 collections. Bone Marrow Transplant 24: 139–145. doi: 10.1038/sj.bmt.1701881
    [33] Clark P, Trickett A, Stark D, et al. (2012) Factors affecting microbial contamination rate of cord blood collected for transplantation. Transfusion 52: 1770–1777. doi: 10.1111/j.1537-2995.2011.03507.x
  • Reader Comments
  • © 2017 the Author(s), licensee AIMS Press. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0)
通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

Metrics

Article views(3672) PDF downloads(1050) Cited by(1)

Article outline

/

DownLoad:  Full-Size Img  PowerPoint
Return
Return

Catalog