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Article: 3D-Printed Atsttrin-Incorporated Alginate/Hydroxyapatite Scaffold Promotes Bone Defect Regeneration with TNF/TNFR Signaling Involvement

Title3D-Printed Atsttrin-Incorporated Alginate/Hydroxyapatite Scaffold Promotes Bone Defect Regeneration with TNF/TNFR Signaling Involvement
Authors
KeywordsAtsttrin
Bioprints
Bone regeneration
Scaffolds
TNF-α
Issue Date2015
PublisherWiley - V C H Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www.wiley.com/bw/journal.asp?ref=2192-2640
Citation
Advanced Healthcare Materials, 2015, v. 4 n. 11, p. 1701-1708 How to Cite?
AbstractHigh expression levels of pro-inflammatory tumor necrosis factor (TNF)-α within bone defects can decelerate and impair bone regeneration. However, there are few available bone scaffolds with anti-inflammatory function. The progranulin (PGRN)-derived engineered protein, Atsttrin, is known to exert antagonistic effects on the TNF-α function. Hence, this study investigates whether 3D-printed Atsttrin-incorporated alginate(Alg)/hydroxyapatite(nHAp) scaffolds can facilitate bone healing through affecting the TNF/TNFR signaling. A 3D bioprinting system is used to fabricate Atsttrin-Alg/nHAp composite scaffolds, and the Atsttrin release from this scaffold is characterized, followed by evaluation of its efficacy on bone regeneration both in vitro and in vivo. The 3D-printed Atsttrin-Alg/nHAp scaffold exhibits a precisely defined structure, can sustain Atsttrin release for at least 5 days, has negligible cytotoxicity, and supports cell adhesion. Atsttrin can also attenuate the suppressive effects of TNF-α on BMP-2-induced osteoblastic differentiation in vitro. The 3D-printed Atsttrin-Alg/nHAp scaffold significantly reduces the number of TNF-α positive cells within wound sites, 7 days after post-calvarial defect surgery. Additionally, histological staining and X-ray scanning results also show that the 3D-printed Atsttrin-Alg/nHAp scaffold enhances the regeneration of mice calvarial bone defects. These findings thus demonstrate that the precise structure and anti-inflammatory properties of 3D-printed Atsttrin-Alg/nHAp scaffolds may promote bone defect repair.
Persistent Identifierhttp://hdl.handle.net/10722/234477
ISSN
2023 Impact Factor: 10.0
2023 SCImago Journal Rankings: 2.337
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorWang, Q-
dc.contributor.authorXia, Q-
dc.contributor.authorWu, Y-
dc.contributor.authorZhang, X-
dc.contributor.authorWen, F-
dc.contributor.authorChen, X-
dc.contributor.authorZhang, S-
dc.contributor.authorHeng, BCA-
dc.contributor.authorHe, Y-
dc.contributor.authorOuyang, HW-
dc.date.accessioned2016-10-14T13:47:08Z-
dc.date.available2016-10-14T13:47:08Z-
dc.date.issued2015-
dc.identifier.citationAdvanced Healthcare Materials, 2015, v. 4 n. 11, p. 1701-1708-
dc.identifier.issn2192-2640-
dc.identifier.urihttp://hdl.handle.net/10722/234477-
dc.description.abstractHigh expression levels of pro-inflammatory tumor necrosis factor (TNF)-α within bone defects can decelerate and impair bone regeneration. However, there are few available bone scaffolds with anti-inflammatory function. The progranulin (PGRN)-derived engineered protein, Atsttrin, is known to exert antagonistic effects on the TNF-α function. Hence, this study investigates whether 3D-printed Atsttrin-incorporated alginate(Alg)/hydroxyapatite(nHAp) scaffolds can facilitate bone healing through affecting the TNF/TNFR signaling. A 3D bioprinting system is used to fabricate Atsttrin-Alg/nHAp composite scaffolds, and the Atsttrin release from this scaffold is characterized, followed by evaluation of its efficacy on bone regeneration both in vitro and in vivo. The 3D-printed Atsttrin-Alg/nHAp scaffold exhibits a precisely defined structure, can sustain Atsttrin release for at least 5 days, has negligible cytotoxicity, and supports cell adhesion. Atsttrin can also attenuate the suppressive effects of TNF-α on BMP-2-induced osteoblastic differentiation in vitro. The 3D-printed Atsttrin-Alg/nHAp scaffold significantly reduces the number of TNF-α positive cells within wound sites, 7 days after post-calvarial defect surgery. Additionally, histological staining and X-ray scanning results also show that the 3D-printed Atsttrin-Alg/nHAp scaffold enhances the regeneration of mice calvarial bone defects. These findings thus demonstrate that the precise structure and anti-inflammatory properties of 3D-printed Atsttrin-Alg/nHAp scaffolds may promote bone defect repair.-
dc.languageeng-
dc.publisherWiley - V C H Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www.wiley.com/bw/journal.asp?ref=2192-2640-
dc.relation.ispartofAdvanced Healthcare Materials-
dc.rightspostprint: This is the accepted version of the following article: FULL CITE, which has been published in final form at [Link to final article]. Preprint This is the pre-peer reviewed version of the following article: FULL CITE, which has been published in final form at [Link to final article].-
dc.subjectAtsttrin-
dc.subjectBioprints-
dc.subjectBone regeneration-
dc.subjectScaffolds-
dc.subjectTNF-α-
dc.title3D-Printed Atsttrin-Incorporated Alginate/Hydroxyapatite Scaffold Promotes Bone Defect Regeneration with TNF/TNFR Signaling Involvement-
dc.typeArticle-
dc.identifier.emailHeng, BCA: alexish@hku.hk-
dc.identifier.doi10.1002/adhm.201500211-
dc.identifier.scopuseid_2-s2.0-84938740625-
dc.identifier.hkuros270333-
dc.identifier.volume4-
dc.identifier.issue11-
dc.identifier.spage1701-
dc.identifier.epage1708-
dc.identifier.isiWOS:000359382600013-
dc.publisher.placeGermany-
dc.identifier.issnl2192-2640-

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