scholarly journals Mineralized collagen scaffolds fabricated with amniotic membrane matrix increase osteogenesis under inflammatory conditions

2020 ◽  
Vol 7 (3) ◽  
pp. 247-258
Author(s):  
Marley J Dewey ◽  
Eileen M Johnson ◽  
Simona T Slater ◽  
Derek J Milner ◽  
Matthew B Wheeler ◽  
...  

Abstract Defects in craniofacial bones occur congenitally, after high-energy impacts, and during the course of treatment for stroke and cancer. These injuries are difficult to heal due to the overwhelming size of the injury area and the inflammatory environment surrounding the injury. Significant inflammatory response after injury may greatly inhibit regenerative healing. We have developed mineralized collagen scaffolds that can induce osteogenic differentiation and matrix biosynthesis in the absence of osteogenic media or supplemental proteins. The amniotic membrane is derived from placentas and has been recently investigated as an extracellular matrix to prevent chronic inflammation. Herein, we hypothesized that a mineralized collagen–amnion composite scaffold could increase osteogenic activity in the presence of inflammatory cytokines. We report mechanical properties of a mineralized collagen–amnion scaffold and investigated osteogenic differentiation and mineral deposition of porcine adipose-derived stem cells within these scaffolds as a function of inflammatory challenge. Incorporation of amniotic membrane matrix promotes osteogenesis similarly to un-modified mineralized collagen scaffolds, and increases in mineralized collagen–amnion scaffolds under inflammatory challenge. Together, these findings suggest that a mineralized collagen–amnion scaffold may provide a beneficial environment to aid craniomaxillofacial bone repair, especially in the course of defects presenting significant inflammatory complications.

2020 ◽  
Author(s):  
Marley J. Dewey ◽  
Eileen M. Johnson ◽  
Simona T. Slater ◽  
Derek J. Milner ◽  
Matthew B. Wheeler ◽  
...  

ABSTRACTDefects in craniofacial bones occur congenitally, after high-energy impacts, and during the course of treatment for stroke and cancer. These injuries are difficult to heal due to the overwhelming size of the injury area and the inflammatory environment surrounding the injury. Significant inflammatory response after injury may greatly inhibit regenerative healing. We have developed mineralized collagen scaffolds that can induce osteogenic differentiation and matrix biosynthesis in the absence of osteogenic media or supplemental proteins. The amniotic membrane is derived from placentas and has been recently investigated as an extracellular matrix to prevent chronic inflammation. Herein, we hypothesized that a mineralized collagen-amnion composite scaffold could increase osteogenic activity in the presence of inflammatory cytokines. We report mechanical properties of a mineralized collagen-amnion scaffold and investigated osteogenic differentiation and mineral deposition of porcine adipose derived stem cells within these scaffolds as a function of inflammatory challenge. Incorporation of amniotic membrane matrix promotes osteogenesis similarly to un-modified mineralized collagen scaffolds, and increases in mineralized collagen-amnion scaffolds under inflammatory challenge. Together, these findings suggest that a mineralized collagen-amnion scaffold may provide a beneficial environment to aid craniomaxillofacial bone repair, especially in the course of defects presenting significant inflammatory complications.


2016 ◽  
Vol 104 (6) ◽  
pp. 1332-1342 ◽  
Author(s):  
Rebecca A. Hortensius ◽  
Jill H. Ebens ◽  
Brendan A. C. Harley

2016 ◽  
Vol 6 (1) ◽  
pp. 20150070 ◽  
Author(s):  
Lester J. Smith ◽  
Alix C. Deymier ◽  
John J. Boyle ◽  
Zhen Li ◽  
Stephen W. Linderman ◽  
...  

Functionally graded, mineralized collagen tissues exist at soft-to-hard material attachments throughout the body. However, the details of how collagen and hydroxyapatite mineral (HA) interact are not fully understood, hampering efforts to develop tissue-engineered constructs that can assist with repair of injuries at the attachments of soft tissues to bone. In this study, spatial control of mineralization was achieved in collagen matrices using simulated body fluids (SBFs). Based upon previous observations of poor bonding between reconstituted collagen and HA deposited using SBF, we hypothesized that mineralizing collagen in the presence of fetuin (which inhibits surface mineralization) would lead to more mineral deposition within the scaffold and therefore a greater increase in stiffness and toughness compared with collagen mineralized without fetuin. We tested this hypothesis through integrated synthesis, mechanical testing and modelling of graded, mineralized reconstituted collagen constructs. Results supported the hypothesis, and further suggested that mineralization on the interior of reconstituted collagen constructs, as promoted by fetuin, led to superior bonding between HA and collagen. The results provide us guidance for the development of mineralized collagen scaffolds, with implications for bone and tendon-to-bone tissue engineering.


Biomaterials ◽  
2012 ◽  
Vol 33 (2) ◽  
pp. 455-463 ◽  
Author(s):  
Yi-Jane Chen ◽  
Min-Chun Chung ◽  
Chung-Chen Jane Yao ◽  
Chien-Hsun Huang ◽  
Hao-Hueng Chang ◽  
...  

2015 ◽  
Vol 3 (3) ◽  
pp. 533-542 ◽  
Author(s):  
Daniel W. Weisgerber ◽  
Steven R. Caliari ◽  
Brendan A. C. Harley

Incorporating calcium phosphate nanocrystallites into a collagen biomaterial promotes mesenchymal stem cell (MSC) osteogenic differentiation in the absence of conventional growth factor supplements. Mineralized collagen scaffolds also support MSC proliferation and new matrix biosynthesis.


Cytotherapy ◽  
2020 ◽  
Vol 22 (5) ◽  
pp. S183
Author(s):  
L. Luo ◽  
H. Uludag ◽  
E. Sone ◽  
S. Viswanathan

2020 ◽  
Author(s):  
Aleczandria S. Tiffany ◽  
Marley J. Dewey ◽  
Brendan A.C. Harley

ABSTRACTTrauma induced injuries of the mouth, jaw, face, and related structures present unique clinical challenges due to their large size and complex geometry. Growth factor signaling coordinates the behavior of multiple cell types following an injury, and effective coordination of growth factor availability within a biomaterial can be critical for accelerating bone healing. Mineralized collagen scaffolds are a class of degradable biomaterial whose biophysical and compositional parameters can be adjusted to facilitate cell invasion and tissue remodeling. Here we describe the use of modified simulated body fluid treatments to enable sequential sequestration of bone morphogenic protein 2 and vascular endothelial growth factor into mineralized collagen scaffolds for bone repair. We report the capability of these scaffolds to sequester growth factors from solution without additional crosslinking treatments and show high levels of retention for individual and multiple growth factors that can be layered into the material via sequential sequestration steps. Sequentially sequestering growth factors allows prolonged release of growth factors in vitro and suggests the potential to improve healing of large-scale bone injury models in vivo. Future work will utilize this sequestration method to induce cellular activities critical to bone healing such as vessel formation and cell migration.


2019 ◽  
Vol 5 (6) ◽  
pp. eaaw4991 ◽  
Author(s):  
Xiaoyan Ren ◽  
Qi Zhou ◽  
David Foulad ◽  
Aleczandria S. Tiffany ◽  
Marley J. Dewey ◽  
...  

The instructive capabilities of extracellular matrix–inspired materials for osteoprogenitor differentiation have sparked interest in understanding modulation of other cell types within the bone regenerative microenvironment. We previously demonstrated that nanoparticulate mineralized collagen glycosaminoglycan (MC-GAG) scaffolds efficiently induced osteoprogenitor differentiation and bone healing. In this work, we combined adenovirus-mediated delivery of osteoprotegerin (AdOPG), an endogenous anti-osteoclastogenic decoy receptor, in primary human mesenchymal stem cells (hMSCs) with MC-GAG to understand the role of osteoclast inactivation in augmentation of bone regeneration. Simultaneous differentiation of osteoprogenitors on MC-GAG and osteoclast progenitors resulted in bidirectional positive regulation. AdOPG expression did not affect osteogenic differentiation alone. In the presence of both cell types, AdOPG-transduced hMSCs on MC-GAG diminished osteoclast-mediated resorption in direct contact; however, osteoclast-mediated augmentation of osteogenic differentiation was unaffected. Thus, the combination of OPG with MC-GAG may represent a method for uncoupling osteogenic and osteoclastogenic differentiation to augment bone regeneration.


2019 ◽  
Vol 93 ◽  
pp. 86-96 ◽  
Author(s):  
Aleczandria S. Tiffany ◽  
Danielle L. Gray ◽  
Toby J. Woods ◽  
Kiran Subedi ◽  
Brendan A.C. Harley

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