TY - JOUR
T1 - Directing tissue morphogenesis via self-assembly of vascular mesenchymal cells
AU - Chen, Ting-Hsuan
AU - Zhu, Xiaolu
AU - Pan, Leiting
AU - Zeng, Xingjuan
AU - Garfinkel, Alan
AU - Tintut, Yin
AU - Demer, Linda L.
AU - Zhao, Xin
AU - Ho, Chih-Ming
PY - 2012/12
Y1 - 2012/12
N2 - Rebuilding injured tissue for regenerative medicine requires technologies to reproduce tissue/biomaterials mimicking the natural morphology. To reconstitute the tissue pattern, current approaches include using scaffolds with specific structure to plate cells, guiding cell spreading, or directly moving cells to desired locations. However, the structural complexity is limited. Also, the artificially-defined patterns are usually disorganized by cellular self-organization in the subsequent tissue development, such as cell migration and cell-cell communication. Here, by working in concert with cellular self-organization rather than against it, we experimentally and mathematically demonstrate a method which directs self-organizing vascular mesenchymal cells (VMCs) to assemble into desired multicellular patterns. Incorporating the inherent chirality of VMCs revealed by interfacing with microengineered substrates and VMCs' spontaneous aggregation, differences in distribution of initial cell plating can be amplified into the formation of striking radial structures or concentric rings, mimicking the cross-sectional structure of liver lobules or osteons, respectively. Furthermore, when co-cultured with VMCs, non-pattern-forming endothelial cells (ECs) tracked along the VMCs and formed a coherent radial or ring pattern in a coordinated manner, indicating that this method is applicable to heterotypical cell organization. © 2012 Elsevier Ltd.
AB - Rebuilding injured tissue for regenerative medicine requires technologies to reproduce tissue/biomaterials mimicking the natural morphology. To reconstitute the tissue pattern, current approaches include using scaffolds with specific structure to plate cells, guiding cell spreading, or directly moving cells to desired locations. However, the structural complexity is limited. Also, the artificially-defined patterns are usually disorganized by cellular self-organization in the subsequent tissue development, such as cell migration and cell-cell communication. Here, by working in concert with cellular self-organization rather than against it, we experimentally and mathematically demonstrate a method which directs self-organizing vascular mesenchymal cells (VMCs) to assemble into desired multicellular patterns. Incorporating the inherent chirality of VMCs revealed by interfacing with microengineered substrates and VMCs' spontaneous aggregation, differences in distribution of initial cell plating can be amplified into the formation of striking radial structures or concentric rings, mimicking the cross-sectional structure of liver lobules or osteons, respectively. Furthermore, when co-cultured with VMCs, non-pattern-forming endothelial cells (ECs) tracked along the VMCs and formed a coherent radial or ring pattern in a coordinated manner, indicating that this method is applicable to heterotypical cell organization. © 2012 Elsevier Ltd.
KW - Co-culture
KW - Mesenchymal stem cell
KW - Micropatterning
KW - Self-assembly
UR - http://www.scopus.com/inward/record.url?scp=84867143819&partnerID=8YFLogxK
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-84867143819&origin=recordpage
U2 - 10.1016/j.biomaterials.2012.08.067
DO - 10.1016/j.biomaterials.2012.08.067
M3 - RGC 21 - Publication in refereed journal
C2 - 23010575
SN - 0142-9612
VL - 33
SP - 9019
EP - 9026
JO - Biomaterials
JF - Biomaterials
IS - 35
ER -