4. The promises of tissue engineering for organ building and banking
With aging population, increase in longevity and decrease in the number of qualified donors, the need to find alternative solutions to current organ replacement methods is rapidly becoming a critical issue. Tissue engineering has appeared as a potentially viable solution. Classical tissue engineerin...
Saved in:
Published in | Cryobiology Vol. 71; no. 1; pp. 165 - 166 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Inc
01.08.2015
|
Online Access | Get full text |
Cover
Loading…
Abstract | With aging population, increase in longevity and decrease in the number of qualified donors, the need to find alternative solutions to current organ replacement methods is rapidly becoming a critical issue. Tissue engineering has appeared as a potentially viable solution. Classical tissue engineering is based on culturing cells in scaffolds, artificial extracellular matrix mimics, with the hope that the process leads to tissues and organs, that upon implantation can replace damaged, dysfunctional ones and lead to regeneration. However, building extensive living structures, such as tissues and organs is a task of monumental complexity. A recent approach to aid this endeavor is bioprinting. In this technique bioink particles, minitissues in the particular method to be described, are deposited into the biopaper, the temporary support structure, with the aid of special-purpose three-dimensional printer, the bioprinter. However, contrary to 3D printing of acellular materials, in the case of bioprinting deposition in itself does not lead to the final product. The functional biological structure results from the post-printing maturation, under near physiological conditions in bioreactors, a process that relies on fundamental early developmental processes akin to those used in embryonic morphogenesis and with no counterpart in the case of printing inanimate substance.
With the recent advances in tissue engineering in general and bioprinting in particular, preservation of the biological structures will soon become an indispensable part of the process. Three possible approaches to the preservation of the engineered tissues and organs seem to emerge, depending on their location in the body or the specific method of their preparation. One approach is to establish a depository of ready-to-use, of-the-shelf replacement organs. This will require the same preservation solutions that are currently used or under development for donor organs. In particular, this approach will benefit from efficient ways of storing and managing organs. This in turn would increase the demand for tissue engineered products, lead to increased funding of the field and eventually result in saving more lives or improving the quality of many patients’ lives. Another possible approach is that the postprinting maturation process takes place in vivo, utilizing the body, the ultimate bioreactor. This approach is limited to non-vital organs or cases where the original organ is not yet fully dysfunctional. Here, it is the recipient organism that carries out the preservation function until the engineered structure becomes fully functional. Finally, in case of in vivo bioprinting, the deposition of the cellular material is performed directly in the recipient. This approach is limited to parts of the body that are accessible for printing, such as skin. The latter two solutions are inherent to tissue engineering.
Novel methods of biofabricating functional tissues and organs, based on tissue engineering technologies thus may offer an alternative solution to mitigating the chronic shortage of donor organs including their preservation. |
---|---|
AbstractList | With aging population, increase in longevity and decrease in the number of qualified donors, the need to find alternative solutions to current organ replacement methods is rapidly becoming a critical issue. Tissue engineering has appeared as a potentially viable solution. Classical tissue engineering is based on culturing cells in scaffolds, artificial extracellular matrix mimics, with the hope that the process leads to tissues and organs, that upon implantation can replace damaged, dysfunctional ones and lead to regeneration. However, building extensive living structures, such as tissues and organs is a task of monumental complexity. A recent approach to aid this endeavor is bioprinting. In this technique bioink particles, minitissues in the particular method to be described, are deposited into the biopaper, the temporary support structure, with the aid of special-purpose three-dimensional printer, the bioprinter. However, contrary to 3D printing of acellular materials, in the case of bioprinting deposition in itself does not lead to the final product. The functional biological structure results from the post-printing maturation, under near physiological conditions in bioreactors, a process that relies on fundamental early developmental processes akin to those used in embryonic morphogenesis and with no counterpart in the case of printing inanimate substance.
With the recent advances in tissue engineering in general and bioprinting in particular, preservation of the biological structures will soon become an indispensable part of the process. Three possible approaches to the preservation of the engineered tissues and organs seem to emerge, depending on their location in the body or the specific method of their preparation. One approach is to establish a depository of ready-to-use, of-the-shelf replacement organs. This will require the same preservation solutions that are currently used or under development for donor organs. In particular, this approach will benefit from efficient ways of storing and managing organs. This in turn would increase the demand for tissue engineered products, lead to increased funding of the field and eventually result in saving more lives or improving the quality of many patients’ lives. Another possible approach is that the postprinting maturation process takes place in vivo, utilizing the body, the ultimate bioreactor. This approach is limited to non-vital organs or cases where the original organ is not yet fully dysfunctional. Here, it is the recipient organism that carries out the preservation function until the engineered structure becomes fully functional. Finally, in case of in vivo bioprinting, the deposition of the cellular material is performed directly in the recipient. This approach is limited to parts of the body that are accessible for printing, such as skin. The latter two solutions are inherent to tissue engineering.
Novel methods of biofabricating functional tissues and organs, based on tissue engineering technologies thus may offer an alternative solution to mitigating the chronic shortage of donor organs including their preservation. |
Author | Norotte, Cyrille Marga, Francoise Forgacs, Gabor Jakab, Karoly |
Author_xml | – sequence: 1 givenname: Karoly surname: Jakab fullname: Jakab, Karoly organization: Department of Physics, University of Missouri-Columbia, MO 65211, United States – sequence: 2 givenname: Francoise surname: Marga fullname: Marga, Francoise organization: Department of Physics, University of Missouri-Columbia, MO 65211, United States – sequence: 3 givenname: Cyrille surname: Norotte fullname: Norotte, Cyrille organization: Department of Physics, University of Missouri-Columbia, MO 65211, United States – sequence: 4 givenname: Gabor surname: Forgacs fullname: Forgacs, Gabor organization: Department of Physics, University of Missouri-Columbia, MO 65211, United States |
BookMark | eNqFkN1KAzEQhYNUsK2-guQFdp1J9qe5U-ovFLyp12GTndTUNilJK_Tt3VK9Fg7MYeAcDt-EjUIMxNgtQomAzd26tOkYjY-bUgDWJQxCuGBjBAWFkEqM2BgAsRCigis2yXkNAE0rqzF7rEq-_CS-S3HrM2UeHd_7nA_EKax8IEo-rLiLice06gI3B7_pT68u9Nx04Wvw1-zSdZtMN793yj6en5bz12Lx_vI2f1gUFusWCqMABcxcbY1qyRBCpVp0CiWazhpHWCkjetWAUCQlKgOGZihrZXtq6k5OWXPutSnmnMjpXfLbLh01gj6x0Gv9x0KfWGgYhDAE789BGtZ9e0o6W0_BUu8T2b3uo_-v4gerp2zT |
CitedBy_id | crossref_primary_10_1186_s41100_019_0218_7 crossref_primary_10_2217_nnm_2016_0088 crossref_primary_10_1002_jcp_28415 |
ContentType | Journal Article |
Copyright | 2015 |
Copyright_xml | – notice: 2015 |
DBID | AAYXX CITATION |
DOI | 10.1016/j.cryobiol.2015.05.010 |
DatabaseName | CrossRef |
DatabaseTitle | CrossRef |
DatabaseTitleList | |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Biology |
EISSN | 1090-2392 |
EndPage | 166 |
ExternalDocumentID | 10_1016_j_cryobiol_2015_05_010 S0011224015001169 |
GroupedDBID | --- --K --M -~X .GJ .~1 0R~ 186 1B1 1RT 1~. 1~5 29F 4.4 457 4G. 53G 5GY 5RE 5VS 6J9 7-5 71M 8P~ 9JM AABVA AACTN AAEDT AAEDW AAIAV AAIKJ AAKOC AALCJ AALRI AAOAW AAQFI AAQXK AATLK AAXUO ABBQC ABFRF ABGRD ABGSF ABJNI ABKYH ABLVK ABMAC ABMZM ABRWV ABTAH ABUDA ABXDB ABYKQ ACDAQ ACGFO ACGFS ACRLP ADBBV ADEZE ADFGL ADMUD ADQTV ADUVX AEBSH AEFWE AEHWI AEKER AENEX AEQOU AESVU AEXOQ AFFNX AFKWA AFTJW AFXIZ AGHFR AGRDE AGUBO AGYEJ AHHHB AIEXJ AIKHN AITUG AJBFU AJOXV AJRQY ALMA_UNASSIGNED_HOLDINGS AMFUW AMRAJ ANZVX ASPBG AVWKF AXJTR AZFZN BKOJK BLXMC BNPGV CAG CBWCG COF CS3 DM4 DOVZS DU5 EBS EFBJH EFLBG EJD EO8 EO9 EP2 EP3 F5P FDB FEDTE FGOYB FIRID FNPLU FYGXN G-Q GBLVA HLV HVGLF HZ~ H~9 IHE J1W KOM LCYCR LG5 LW8 M41 MO0 N9A O-L O9- OAUVE OZT P-8 P-9 P2P PC. Q38 QYZTP R2- RIG ROL RPZ SAB SDF SDG SDP SES SEW SNL SPCBC SSA SSH SSU SSZ T5K TWZ UHS UNMZH WUQ XPP ZCG ZMT ZXP ZY4 ~02 ~G- ~KM AAHBH AAXKI AAYXX ADVLN AFJKZ AKRWK CITATION |
ID | FETCH-LOGICAL-c1570-b901208f5cb97ebe104971f9131bacbfe149b2d96029e3319b0be81359cde65a3 |
IEDL.DBID | AIKHN |
ISSN | 0011-2240 |
IngestDate | Thu Sep 26 18:34:12 EDT 2024 Fri Feb 23 02:23:41 EST 2024 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 1 |
Language | English |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c1570-b901208f5cb97ebe104971f9131bacbfe149b2d96029e3319b0be81359cde65a3 |
PageCount | 2 |
ParticipantIDs | crossref_primary_10_1016_j_cryobiol_2015_05_010 elsevier_sciencedirect_doi_10_1016_j_cryobiol_2015_05_010 |
PublicationCentury | 2000 |
PublicationDate | August 2015 2015-08-00 |
PublicationDateYYYYMMDD | 2015-08-01 |
PublicationDate_xml | – month: 08 year: 2015 text: August 2015 |
PublicationDecade | 2010 |
PublicationTitle | Cryobiology |
PublicationYear | 2015 |
Publisher | Elsevier Inc |
Publisher_xml | – name: Elsevier Inc |
SSID | ssj0006734 |
Score | 2.1251183 |
Snippet | With aging population, increase in longevity and decrease in the number of qualified donors, the need to find alternative solutions to current organ... |
SourceID | crossref elsevier |
SourceType | Aggregation Database Publisher |
StartPage | 165 |
Title | 4. The promises of tissue engineering for organ building and banking |
URI | https://dx.doi.org/10.1016/j.cryobiol.2015.05.010 |
Volume | 71 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV07a8MwED7yoNCl9EnTR9DQ1YkVWbE1hrQhbWmmBrIJyZEgGZzQpEOW_vaeLLlNodCh4MUGgbmzvvs-6x4AdyJj1CqTRImleYQ70UQadQiCocH4qiySDPdD_2XSH0-Tpxmf1WBY1cK4tMqA_R7TS7QOT7rBmt31YuFqfKk7FnKS3Z0miDo0MRwlSQOag8fn8eQLkPsp882YKY3cgr1C4SWq213Z78hleXHfxDP-PUbtxZ3RMRwFwkgG_p1OoGaKUzjwIyR3Z3CfdAi6miAQosfMhqws2ZbGJOa71SBBakrKAU5EhznYRBVzolU5OeEcpqOH1-E4CpMRopzyNI60cDWvmeW5Fim6ATWVSKkVlFGtcm0N6h7dm6M66QnDcJfpWJuMMi7yuelzxS6gUawKcwkk4YZxqzjKDKRGCgWxRhLVU5lC5qRz24JuZQu59g0wZJUZtpSV9aSznozxonELRGUy-cOVElH6j7VX_1h7DYfuzmfn3UBj-_ZubpExbHUb6p0P2g7fxSeJjL7Z |
link.rule.ids | 315,786,790,4521,24144,27955,27956,45618,45712 |
linkProvider | Elsevier |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3NT8IwFH9BjNGL8TPiZw9eCytd2Xo0KEEFTpBwa9rRJngYRPHAxb_d13ULmJh4MNlpW5Pl99rX3299HwD3MuXMaRvT2LGM4kq01KAOQWdocX_VDkmG_6E_HHX6k_hlKqY16Fa5MD6ssvT9wacX3rq80yrRbC3nc5_jy_yxkJfs_jRB7sCuZwM-rqv5tYnz6CQ8lGJmjPrXt9KE31DbrotqRz7GS4QSntHvO9TWrtM7gsOSLpKH8EXHULP5CeyFBpLrU3iMmwQNTdANor3sB1k4siqgJHZTaJAgMSVF-yZiyi7YROczYnTRN-EMJr2ncbdPy74INGMiiaiRPuM1dSIzMkEjoKKSCXOScWZ0ZpxF1WPaM9QmbWk5rjETGZsyLmQ2sx2h-TnU80VuL4DEwnLhtECRgcRIoxw2SKHaOtXIm0zmGtCqsFDLUP5CVXFhb6pCT3n0VIQXixogK8jUD0Mq9NF_jL38x9g72O-PhwM1eB69XsGBfxLi9K6hvnr_tDfIHVbmtpgb3zP8v64 |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=4.+The+promises+of+tissue+engineering+for+organ+building+and+banking&rft.jtitle=Cryobiology&rft.au=Jakab%2C+Karoly&rft.au=Marga%2C+Francoise&rft.au=Norotte%2C+Cyrille&rft.au=Forgacs%2C+Gabor&rft.date=2015-08-01&rft.pub=Elsevier+Inc&rft.issn=0011-2240&rft.eissn=1090-2392&rft.volume=71&rft.issue=1&rft.spage=165&rft.epage=166&rft_id=info:doi/10.1016%2Fj.cryobiol.2015.05.010&rft.externalDocID=S0011224015001169 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0011-2240&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0011-2240&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0011-2240&client=summon |