Segmental Additive Tissue Engineering.
Segmental Additive Tissue Engineering.
复制标题
DOI:
10.1038/s41598-018-29270-4
复制
发表时间:
2018-07-18
影响因子:
4.6
通讯作者:
de Peppo GM
中科院分区:
文献类型:
--
作者:
Sladkova M;Alawadhi R;Jaragh Alhaddad R;Esmael A;Alansari S;Saad M;Mulla Yousef J;Alqaoud L;de Peppo GM
Segmental bone defects caused by trauma and disease represent a major clinical problem worldwide. Current treatment options are limited and often associated with poor outcomes and severe complications. Bone engineering is a promising alternative solution, but a number of technical challenges must be addressed to allow for effective and reproducible construction of segmental grafts that meet the size and geometrical requirements needed for individual patients and routine clinical applications. It is important to devise engineering strategies and standard operating procedures that make it possible to scale up the size of bone-engineered grafts, minimize process and product variability, and facilitate technology transfer and implementation. To address these issues, we have combined traditional and modular tissue engineering approaches in a strategy referred to as Segmental Additive Tissue Engineering (SATE). To demonstrate this approach, a digital reconstruction of a rabbit femoral defect was partitioned transversally to the longitudinal axis into segments (modules) with discoidal geometry and defined thickness to enable protocol standardization and effective tissue formation in vitro. Bone grafts corresponding to each segment were then engineered using biomimetic scaffolds seeded with human induced pluripotent stem cell-derived mesodermal progenitors (iPSC-MPs) and a novel perfusion bioreactor with universal design. The SATE strategy enables the effective and reproducible engineering of segmental bone grafts for personalized skeletal reconstruction, and will facilitate technology transfer and implementation of a tissue engineering approach to segmental bone defect therapy.
登录
查看更多内容
影响因子:
10
作者:
Hinderliter PM;Minard KR;Orr G;Chrisler WB;Thrall BD;Pounds JG;Teeguarden JG
通讯作者:
Teeguarden JG
影响因子:
7.8
作者:
Zhou, Shuanhu;Greenberger, Joel S.;Glowacki, Julie
通讯作者:
Glowacki, Julie
影响因子:
56.9
作者:
LANGER, R;VACANTI, JP
通讯作者:
VACANTI, JP
影响因子:
64.5
作者:
Takahashi, Kazutoshi;Tanabe, Koji;Yamanaka, Shinya
通讯作者:
Yamanaka, Shinya
影响因子:
46.9
作者:
Petite, H;Viateau, V;Guillemin, G
通讯作者:
Guillemin, G