TY - JOUR
T1 - Embedding cells within nanoscale, rapidly mineralizing hydrogels
T2 - A new paradigm to engineer cell-laden bone-like tissue
AU - Mansoorifar, Amin
AU - Subbiah, Ramesh
AU - Balbinot, Gabriela de Souza
AU - Parthiban, Selvakumar Prakash
AU - Bertassoni, Luiz E.
N1 - Funding Information:
This project was partly supported by funding from the National Institute of Dental and Craniofacial Research (R01DE026170 and 3R01DE026170-03S1) and the Oregon Clinical & Translational Research Institute (OCTRI) - Biomedical Innovation Program (BIP).
Publisher Copyright:
© 2020
PY - 2020/12/1
Y1 - 2020/12/1
N2 - Bone mineralization is a highly specific and dynamic nanoscale process that has been studied extensively from a structural, chemical, and biological standpoint. Bone tissue, therefore, may be defined by the interplay of its intricately mineralized matrix and the cells that regulate its biological function. However, the far majority of engineered bone model systems and bone replacement materials have been unable to replicate this key characteristic of bone tissue; that is, the ability of cells to be gradually and rapidly embedded in a three-dimensional (3D) heavily calcified matrix material. Here we review the characteristics that define the bone matrix from a nanostructural perspective. We then revisit the benefits and challenges of existing model systems and engineered bone replacement materials, and discuss recent efforts to replicate the biological, cellular, mechanical, and materials characteristics of bone tissue on the nano- to microscale. We pay particular attention to a recently proposed method developed by our group, which seeks to replicate key aspects of the entrapment of bone cells within a mineralized matrix with precisions down to the level of individual nano-crystallites, inclusive of the bone vasculature, and osteogenic differentiation process. In summary, this paper discusses existing and emerging evidence pointing towards future developments bridging the gap between the fields of biomineralization, structural biology, stem cells, and tissue engineering, which we believe will hold the key to engineer truly functional bone-like tissue in the laboratory.
AB - Bone mineralization is a highly specific and dynamic nanoscale process that has been studied extensively from a structural, chemical, and biological standpoint. Bone tissue, therefore, may be defined by the interplay of its intricately mineralized matrix and the cells that regulate its biological function. However, the far majority of engineered bone model systems and bone replacement materials have been unable to replicate this key characteristic of bone tissue; that is, the ability of cells to be gradually and rapidly embedded in a three-dimensional (3D) heavily calcified matrix material. Here we review the characteristics that define the bone matrix from a nanostructural perspective. We then revisit the benefits and challenges of existing model systems and engineered bone replacement materials, and discuss recent efforts to replicate the biological, cellular, mechanical, and materials characteristics of bone tissue on the nano- to microscale. We pay particular attention to a recently proposed method developed by our group, which seeks to replicate key aspects of the entrapment of bone cells within a mineralized matrix with precisions down to the level of individual nano-crystallites, inclusive of the bone vasculature, and osteogenic differentiation process. In summary, this paper discusses existing and emerging evidence pointing towards future developments bridging the gap between the fields of biomineralization, structural biology, stem cells, and tissue engineering, which we believe will hold the key to engineer truly functional bone-like tissue in the laboratory.
KW - Biomineralization
KW - Bone
KW - Cell-laden hydrogel
KW - PILP
KW - Vascularization
UR - http://www.scopus.com/inward/record.url?scp=85092717587&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85092717587&partnerID=8YFLogxK
U2 - 10.1016/j.jsb.2020.107636
DO - 10.1016/j.jsb.2020.107636
M3 - Review article
C2 - 33039511
AN - SCOPUS:85092717587
SN - 1047-8477
VL - 212
JO - Journal of Structural Biology
JF - Journal of Structural Biology
IS - 3
M1 - 107636
ER -