東華大學圖書館 |

語系: 繁體中文

說明(常見問題)

回圖書館首頁

手機版館藏查詢

登入

回首頁

切換: 標籤 | MARC模式 | ISBD

Growth and remodeling in engineered ...

Olberding, Joseph E.

FindBook

Google Book

Amazon

博客來

Growth and remodeling in engineered soft tissue.

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
正題名/作者:	Growth and remodeling in engineered soft tissue./
作者:	Olberding, Joseph E.
面頁冊數:	146 p.
附註:	Source: Dissertation Abstracts International, Volume: 71-12, Section: B, page: 7557.
Contained By:	Dissertation Abstracts International71-12B.
標題:	Engineering, Biomedical. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3429487
ISBN:	9781124285351

Growth and remodeling in engineered soft tissue.
Olberding, Joseph E.

Growth and remodeling in engineered soft tissue. - 146 p.

Source: Dissertation Abstracts International, Volume: 71-12, Section: B, page: 7557.

Thesis (Ph.D.)--University of Michigan, 2010.

Left to their own devices, tendons and ligaments repair slowly due to low blood flow and cell content. An engineered tissue contruct (ETC) approach using multi- potent bone marrow stromal cells (MSCs) without an exogenous scaffold promises a robust autologous intervention strategy. From a biomechanical perspective, two physical processes govern the development of ETCs in vitro: growth, such as protein deposition or cell proliferation, and remodeling, such as fiber reorientation or cell differentiation. This dissertation describes the development and analysis of biomechanical models of growth and remodeling critical to scaffold-less soft tissue engineering.

ISBN: 9781124285351Subjects--Topical Terms:

1017684
Engineering, Biomedical.

Growth and remodeling in engineered soft tissue.
LDR:03495nam 2200349 4500 001 1404607
005 20111130124056.5
008 130515s2010 ||||||||||||||||| ||eng d
020 $a 9781124285351
035 $a (UMI)AAI3429487
035 $a AAI3429487
040 $a UMI $c UMI
100 1 $a Olberding, Joseph E. $3 1683940
245 1 0 $a Growth and remodeling in engineered soft tissue.
300 $a 146 p.
500 $a Source: Dissertation Abstracts International, Volume: 71-12, Section: B, page: 7557.
500 $a Advisers: Krishnakumar R. Garikipati; Karl Grosh.
502 $a Thesis (Ph.D.)--University of Michigan, 2010.
520 $a Left to their own devices, tendons and ligaments repair slowly due to low blood flow and cell content. An engineered tissue contruct (ETC) approach using multi- potent bone marrow stromal cells (MSCs) without an exogenous scaffold promises a robust autologous intervention strategy. From a biomechanical perspective, two physical processes govern the development of ETCs in vitro: growth, such as protein deposition or cell proliferation, and remodeling, such as fiber reorientation or cell differentiation. This dissertation describes the development and analysis of biomechanical models of growth and remodeling critical to scaffold-less soft tissue engineering.
520 $a Firstly, the thermodynamics of a class of fiber remodeling laws were investigated in detail. It was found that purely mechanical formulations of remodeling that stiffen tissue are thermodynamically inadmissible. This dissipation imbalance was quantified in a finite-element model of tendon undergoing fiber reorientation and was found to be positive under both constant displacement and constant load boundary conditions.
520 $a Next, a novel image processing algorithm was developed to quantify directionality in planar and volumetric image data for incorporation into continuum mechanical models. With a single input parameter, the method was validated in 2D against representative synthetic images of known fiber distributions and was able to distinguish in 3D between isotropic and fibroblast-aligned collagen gels imaged using confocal microscopy.
520 $a To optimize the ETC culture system for tendon and ligament, the effects of oxygen content were studied on the growth and fibroblastic differentiation of rat MSCs and tendon fibroblasts (TFbs). A1SCs exhibited a significantly shorter population doubling time under hypoxic conditions (5% O2) compared to normoxia (18% O2). Collagen I m13,NA and protein levels increased significantly up to 2d in hypoxic MSC culture. Both cell types demonstrated elevated inR,1 As encoding the tendon and ligament-associated transcription factor scleraxis under hypoxia.
520 $a Besides the individual contributions of these studies, the ability to model and simulate complex cell and tissue behaviors---both computationally and experimentally---portends not only patient-specific engineered tissue therapies using "computer-aided tissue engineering", but also enables the testing of hypotheses related to important biological questions not directly approachable via conventional experiments.
590 $a School code: 0127.
650 4 $a Engineering, Biomedical. $3 1017684
650 4 $a Biophysics, Biomechanics. $3 1035342
650 4 $a Biophysics, General. $3 1019105
690 $a 0541
690 $a 0648
690 $a 0786
710 2 $a University of Michigan. $3 777416
773 0 $t Dissertation Abstracts International $g 71-12B.
790 1 0 $a Garikipati, Krishnakumar R., $e advisor
790 1 0 $a Grosh, Karl, $e advisor
790 $a 0127
791 $a Ph.D.
792 $a 2010
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3429487