The independent role of cyclic flexure in the early in vitro development of an engineered heart valve tissue

Biomaterials ◽  
2005 ◽  
Vol 26 (2) ◽  
pp. 175-187 ◽  
Author(s):  
George C Engelmayr ◽  
Elena Rabkin ◽  
Fraser W.H Sutherland ◽  
Frederick J Schoen ◽  
John E Mayer ◽  
...  
Biomaterials ◽  
2010 ◽  
Vol 31 (6) ◽  
pp. 1114-1125 ◽  
Author(s):  
Sharan Ramaswamy ◽  
Danielle Gottlieb ◽  
George C. Engelmayr ◽  
Elena Aikawa ◽  
David E. Schmidt ◽  
...  

Author(s):  
Chad E. Eckert ◽  
Brandon T. Mikulis ◽  
Dane Gerneke ◽  
Danielle Gottlieb ◽  
Bruce Smaill ◽  
...  

Engineered heart valve tissue (EHVT) has received much attention as a potential pediatric valve replacement therapy, offering prospective long-term functional improvements over current options. A significant gap in the literature exists, however, regarding estimating tissue mechanical properties from tissue-scaffold composites. Detailed three-dimensional structural information prior to implantation (in vitro) and after implantation in (in vivo) is needed for improved modeling of tissue properties. As such, a novel high-resolution imaging technique will be employed to obtain three-dimensional microstructural information. Analysis techniques will be used to fully quantify constituents of interest including scaffold, collagen, and cellular information and to develop appropriate two-dimensional sectioning sampling protocols. It is the intent of this work to guide modeling efforts to better elucidate EHVT tissue-specific mechanical properties.


2014 ◽  
Vol 136 (12) ◽  
Author(s):  
Sharan Ramaswamy ◽  
Steven M. Boronyak ◽  
Trung Le ◽  
Andrew Holmes ◽  
Fotis Sotiropoulos ◽  
...  

The ability to replicate physiological hemodynamic conditions during in vitro tissue development has been recognized as an important aspect in the development and in vitro assessment of engineered heart valve tissues. Moreover, we have demonstrated that studies aiming to understand mechanical conditioning require separation of the major heart valve deformation loading modes: flow, stretch, and flexure (FSF) (Sacks et al., 2009, "Bioengineering Challenges for Heart Valve Tissue Engineering," Annu. Rev. Biomed. Eng., 11(1), pp. 289–313). To achieve these goals in a novel bioreactor design, we utilized a cylindrical conduit configuration for the conditioning chamber to allow for higher fluid velocities, translating to higher shear stresses on the in situ tissue specimens while retaining laminar flow conditions. Moving boundary computational fluid dynamic (CFD) simulations were performed to predict the flow field under combined cyclic flexure and steady flow (cyclic-flex-flow) states using various combinations of flow rate, and media viscosity. The device was successfully constructed and tested for incubator housing, gas exchange, and sterility. In addition, we performed a pilot experiment using biodegradable polymer scaffolds seeded with bone marrow derived stem cells (BMSCs) at a seeding density of 5 × 106 cells/cm2. The constructs were subjected to combined cyclic flexure (1 Hz frequency) and steady flow (Re = 1376; flow rate of 1.06 l/min (LPM); shear stress in the range of 0–9 dynes/cm2) for 2 weeks to permit physiological shear stress conditions. Assays revealed significantly (P < 0.05) higher amounts of collagen (2051 ± 256 μg/g) at the end of 2 weeks in comparison to similar experiments previously conducted in our laboratory but performed at subphysiological levels of shear stress (<2 dynes/cm2; Engelmayr et al., 2006, "Cyclic Flexure and Laminar Flow Synergistically Accelerate Mesenchymal Stem Cell-Mediated Engineered Tissue Formation: Implications for Engineered Heart Valve Tissues," Biomaterials, 27(36), pp. 6083–6095). The implications of this novel design are that fully coupled or decoupled physiological flow, flexure, and stretch modes of engineered tissue conditioning investigations can be readily accomplished with the inclusion of this device in experimental protocols on engineered heart valve tissue formation.


Author(s):  
Sajad A. Beigh ◽  
Wani A. Ahad ◽  
Rumase A. Bhat ◽  
Neelofar Nabi ◽  
Touqeer Ahmed ◽  
...  

Immunology ◽  
1996 ◽  
Vol 89 (4) ◽  
pp. 619-626 ◽  
Author(s):  
L. MATERA ◽  
G. BELLONE ◽  
J.‐J. LEBRUN ◽  
P. A. KELLY ◽  
E. L. HOOGHE PETERS ◽  
...  

2018 ◽  
Vol 43 (2) ◽  
pp. 195-198 ◽  
Author(s):  
Ovandir Bazan ◽  
Márcia M. O. Simbara ◽  
Jayme P. Ortiz ◽  
Sonia M. Malmonge ◽  
Aron Andrade ◽  
...  

2003 ◽  
Vol 49 (4) ◽  
pp. 297-305 ◽  
Author(s):  
Masashi TAKAHASHI ◽  
Hitomi TAKAHASHI ◽  
Seizo HAMANO ◽  
Satoko WATANABE ◽  
Shigeki INUMARU ◽  
...  

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