TY - JOUR
T1 - Biological performance of cell-encapsulated methacrylated gellan gum-based hydrogels for nucleus pulposus regeneration
AU - Tsaryk, Roman
AU - Silva-Correia, Joana
AU - Oliveira, Joaquim Miguel
AU - Unger, Ronald E.
AU - Landes, Constantin
AU - Brochhausen, Christoph
AU - Ghanaati, Shahram
AU - Reis, Rui L.
AU - Kirkpatrick, C. James
N1 - Publisher Copyright:
Copyright © 2014 John Wiley & Sons, Ltd.
PY - 2017/3/1
Y1 - 2017/3/1
N2 - Limitations of current treatments for intervertebral disc (IVD) degeneration have promoted interest in the development of tissue-engineering approaches. Injectable hydrogels loaded with cells can be used as a substitute material for the inner IVD part, the nucleus pulposus (NP), and provide an opportunity for minimally invasive treatment of IVD degeneration. The NP is populated by chondrocyte-like cells; therefore, chondrocytes and mesenchymal stem cells (MSCs), stimulated to differentiate along the chondrogenic lineage, could be used to promote NP regeneration. In this study, the in vitro and in vivo response of human bone marrow-derived MSCs and nasal chondrocytes (NCs) to modified gellan gum-based hydrogels was investigated. Both ionic- (iGG–MA) and photo-crosslinked (phGG–MA) methacrylated gellan gum hydrogels show no cytotoxicity in extraction assays with MSCs and NCs. Furthermore, the materials do not induce pro-inflammatory responses in endothelial cells. Moreover, MSCs and NCs can be encapsulated into the hydrogels and remain viable for at least 2 weeks, although apoptosis is observed in phGG–MA. Importantly, encapsulated MSCs and NCs show signs of in vivo chondrogenesis in a subcutaneous implantation of iGG–MA. Altogether, the data endorse the potential use of modified gellan gum-based hydrogel as a suitable material in NP tissue engineering.
AB - Limitations of current treatments for intervertebral disc (IVD) degeneration have promoted interest in the development of tissue-engineering approaches. Injectable hydrogels loaded with cells can be used as a substitute material for the inner IVD part, the nucleus pulposus (NP), and provide an opportunity for minimally invasive treatment of IVD degeneration. The NP is populated by chondrocyte-like cells; therefore, chondrocytes and mesenchymal stem cells (MSCs), stimulated to differentiate along the chondrogenic lineage, could be used to promote NP regeneration. In this study, the in vitro and in vivo response of human bone marrow-derived MSCs and nasal chondrocytes (NCs) to modified gellan gum-based hydrogels was investigated. Both ionic- (iGG–MA) and photo-crosslinked (phGG–MA) methacrylated gellan gum hydrogels show no cytotoxicity in extraction assays with MSCs and NCs. Furthermore, the materials do not induce pro-inflammatory responses in endothelial cells. Moreover, MSCs and NCs can be encapsulated into the hydrogels and remain viable for at least 2 weeks, although apoptosis is observed in phGG–MA. Importantly, encapsulated MSCs and NCs show signs of in vivo chondrogenesis in a subcutaneous implantation of iGG–MA. Altogether, the data endorse the potential use of modified gellan gum-based hydrogel as a suitable material in NP tissue engineering.
KW - gellan gum
KW - hydrogel
KW - intervertebral disc
KW - mesenchymal stem cells
KW - nasal chondrocytes
KW - nucleus pulposus
UR - http://www.scopus.com/inward/record.url?scp=85015003069&partnerID=8YFLogxK
U2 - 10.1002/term.1959
DO - 10.1002/term.1959
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 25370800
AN - SCOPUS:85015003069
SN - 1932-6254
VL - 11
SP - 637
EP - 648
JO - Journal of Tissue Engineering and Regenerative Medicine
JF - Journal of Tissue Engineering and Regenerative Medicine
IS - 3
ER -