TY - JOUR
T1 - “Tissue Papers” from Organ-Specific Decellularized Extracellular Matrices
AU - Jakus, Adam E.
AU - Laronda, Monica M.
AU - Rashedi, Alexandra S.
AU - Robinson, Christina M.
AU - Lee, Chris
AU - Jordan, Sumanas W.
AU - Orwig, Kyle E.
AU - Woodruff, Teresa K.
AU - Shah, Ramille N.
N1 - Funding Information:
The authors would like to acknowledge Kathrin Gassei (Magee-Womens Research Institute, University of Pittsburgh School of Medicine) for coordinating ovary tissue acquisition and distribution, which is funded by the Departments of Urology and of Obstetrics, Gynecology & Reproductive Sciences at the University of Pittsburgh School of Medicine (K.E.O.), and Michael McRaven and Thomas Hope for acquisition of rhesus macaque ovary tissue. The majority of experiments were performed at the Simpson Querrey Institute for BioNanotechnology at the Northwestern University. The U.S. Army Research Office, the U.S. Army Medical Research and Material Command, and the Northwestern University provided funding to develop this facility. The Northwestern University Center for Advanced Microscopy generously supported by the NCI CCSG P30 CA060553 awarded to the Robert H. Lurie Comprehensive Cancer Center. The authors made use of the EPIC facility (NUANCE Center—Northwestern University) supported by the NSFDMR-1121262 and EEC-0118025|003; the Northwestern University Mouse Histology and Phenotyping Laboratory and Cancer Center supported by the NCI CA060553; the Office of Naval ResearchMURI Program (N00014-11-1-0690). Additional funding support was provided by a gift from Google (R.N.S.). This work was also supported by the Watkins Chair of Obstetrics and Gynecology (T.K.W.), and by the Center for Reproductive Health after Disease (P50 HD076188-02) from the National Centers for Translational Research in Reproduction and Infertility (NCTRI) (T.K.W.), A.E.J. was supported by a postdoctoral fellowship from The Hartwell Foundation. M.M.L. was supported by the Burroughs Wellcome Fund Career Award at the Scientific Interface.
Publisher Copyright:
© 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2017/9/13
Y1 - 2017/9/13
N2 - Using an innovative, tissue-independent approach to decellularized tissue processing and biomaterial fabrication, the development of a series of “tissue papers” derived from native porcine tissues/organs (heart, kidney, liver, muscle), native bovine tissue/organ (ovary and uterus), and purified bovine Achilles tendon collagen as a control from decellularized extracellular matrix particle ink suspensions cast into molds is described. Each tissue paper type has distinct microstructural characteristics as well as physical and mechanical properties, is capable of absorbing up to 300% of its own weight in liquid, and remains mechanically robust (E = 1–18 MPa) when hydrated; permitting it to be cut, rolled, folded, and sutured, as needed. In vitro characterization with human mesenchymal stem cells reveals that all tissue paper types support cell adhesion, viability, and proliferation over four weeks. Ovarian tissue papers support mouse ovarian follicle adhesion, viability, and health in vitro, as well as support, and maintain the viability and hormonal function of nonhuman primate and human follicle-containing, live ovarian cortical tissues ex vivo for eight weeks postmortem. “Tissue papers” can be further augmented with additional synthetic and natural biomaterials, as well as integrated with recently developed, advanced 3D-printable biomaterials, providing a versatile platform for future multi-biomaterial construct manufacturing.
AB - Using an innovative, tissue-independent approach to decellularized tissue processing and biomaterial fabrication, the development of a series of “tissue papers” derived from native porcine tissues/organs (heart, kidney, liver, muscle), native bovine tissue/organ (ovary and uterus), and purified bovine Achilles tendon collagen as a control from decellularized extracellular matrix particle ink suspensions cast into molds is described. Each tissue paper type has distinct microstructural characteristics as well as physical and mechanical properties, is capable of absorbing up to 300% of its own weight in liquid, and remains mechanically robust (E = 1–18 MPa) when hydrated; permitting it to be cut, rolled, folded, and sutured, as needed. In vitro characterization with human mesenchymal stem cells reveals that all tissue paper types support cell adhesion, viability, and proliferation over four weeks. Ovarian tissue papers support mouse ovarian follicle adhesion, viability, and health in vitro, as well as support, and maintain the viability and hormonal function of nonhuman primate and human follicle-containing, live ovarian cortical tissues ex vivo for eight weeks postmortem. “Tissue papers” can be further augmented with additional synthetic and natural biomaterials, as well as integrated with recently developed, advanced 3D-printable biomaterials, providing a versatile platform for future multi-biomaterial construct manufacturing.
KW - biomaterials
KW - decellularized extracellular matrices
KW - ovary tissue engineering
KW - tissue engineering
UR - http://www.scopus.com/inward/record.url?scp=85026743018&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85026743018&partnerID=8YFLogxK
U2 - 10.1002/adfm.201700992
DO - 10.1002/adfm.201700992
M3 - Article
C2 - 29104526
AN - SCOPUS:85026743018
SN - 1616-301X
VL - 27
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 34
M1 - 1700992
ER -