Capillary Network-Like Organization of Endothelial Cells in PEGDA Scaffolds Encoded with Angiogenic Signals via Triple Helical Hybridization.
Capillary Network-Like Organization of Endothelial Cells in PEGDA Scaffolds Encoded with Angiogenic Signals via Triple Helical Hybridization.
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DOI:
10.1002/adfm.201303217
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发表时间:
2014-06-04
影响因子:
19
通讯作者:
Yu, S. M.
中科院分区:
文献类型:
--
作者:
Stahl, Patrick J.;Chan, Tania R.;Shen, Yu-I;Sun, Guoming;Gerecht, Sharon;Yu, S. M.
Survival of tissue engineered constructs after implantation depends on proper vascularization. The differentiation of endothelial cells into mature microvasculature requires dynamic interactions between cells, scaffold, and growth factors, which are difficult to recapitulate in artificial systems. Previously, photocrosslinked poly(ethylene glycol) diacrylate (PEGDA) hydrogels displaying collagen mimetic peptides (CMPs), dubbed PEGDA‐CMP, that can be further conjugated with bioactive molecules via CMP‐CMP triple helix hybridization were reported. Here, it is shown that a bifunctional peptide featuring pro‐angiogenic domain mimicking vascular endothelial growth factor (VEGF) and a collagen mimetic domain that can fold into a triple helix conformation can hybridize with CMP side chains of the PEGDA‐CMP hydrogel, which results in presentation of insoluble VEGF‐like signals to endothelial cells. Presentation of VEGF‐like signals on the surface of micropatterned scaffolds in this way transforms cells from a quiescent state to elongated and aligned phenotype suggesting that this system could be used to engineer organized microvasculature. It is also shown that the pro‐angiogenic peptide, when applied topically in combination with modified dextran/PEGDA hydrogels, can enhance neovascularization of burn wounds in mice demonstrating the potential clinical use of CMP‐mediated matrix‐bound bioactive molecules for dermal injuries.
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影响因子:
12.3
作者:
Carpenter AE;Jones TR;Lamprecht MR;Clarke C;Kang IH;Friman O;Guertin DA;Chang JH;Lindquist RA;Moffat J;Golland P;Sabatini DM
通讯作者:
Sabatini DM
DOI:
10.1073/pnas.0505047102
发表时间:
2005-10-04
影响因子:
11.1
作者:
D'Andrea, LD;Iaccarino, G;Pedone, C
通讯作者:
Pedone, C
影响因子:
3.4
作者:
Dickinson, Laura E.;Moura, Matthew E.;Gerecht, Sharon
通讯作者:
Gerecht, Sharon
影响因子:
14.8
作者:
Brafman, David A.;Chien, Shu;Willert, Karl
通讯作者:
Willert, Karl
影响因子:
4.8
作者:
Ackerman, MS;Bhate, M;Brodsky, B
通讯作者:
Brodsky, B