Creating alignment and anisotropy in engineered heart tissue: role of boundary conditions in a model three-dimensional culture system.

Electrical and mechanical anisotropy arise from matrix and cellular alignment in native myocardium. Generation of anisotropy in engineered heart tissue will be required to match native properties and will provide immediate opportunities to investigate the genesis and structural determinants of functional anisotropy. We investigated the influence of geometry and boundary conditions on fibroblast alignment in thin collagen gels. Consistent with previous reports, we found that human dermal fibroblasts align parallel to free edges in partially constrained gels; in contrast to at least one report, fibroblasts in fully constrained gels remained randomly aligned independent of geometry. These experiments allowed us to distinguish between two possible mechanisms for such alignment. Mean orientations that followed the shape of the free edges and stronger alignment nearest the free edges in gels with a variety of geometries suggested that cells align parallel to a local free boundary rather than to local lines of tension. These findings focus attention on the presence of voids and free surfaces such as the endocardium and epicardium, cleavage planes, and blood vessels in governing cell and fiber alignment in developing and remodeling myocardium, myocardial scar tissue, and engineered heart constructs.

[1]  S. Milam,et al.  Cells transmit spatial information by orienting collagen fibers. , 1989, Matrix.

[2]  G I Zahalak,et al.  The effects of cross-fiber deformation on axial fiber stress in myocardium. , 1999, Journal of biomechanical engineering.

[3]  R. Tranquillo,et al.  Exploiting glycation to stiffen and strengthen tissue equivalents for tissue engineering. , 1999, Journal of biomedical materials research.

[4]  Thomas Eschenhagen,et al.  Chronic stretch of engineered heart tissue induces hypertrophy and functional improvement , 2000, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[5]  R T Tranquillo,et al.  Engineered alignment in media equivalents: magnetic prealignment and mandrel compaction. , 1998, Journal of biomechanical engineering.

[6]  F A Auger,et al.  In vitro construction of a human blood vessel from cultured vascular cells: a morphologic study. , 1993, Journal of vascular surgery.

[7]  J. Ross,et al.  Fiber Orientation in the Canine Left Ventricle during Diastole and Systole , 1969, Circulation research.

[8]  D. L. Bassett,et al.  An engineering analysis of myocardial fiber orientation in pig's left ventricle in systole , 1966 .

[9]  J W Covell,et al.  Transverse shear along myocardial cleavage planes provides a mechanism for normal systolic wall thickening. , 1995, Circulation research.

[10]  R T Tranquillo,et al.  An anisotropic biphasic theory of tissue-equivalent mechanics: the interplay among cell traction, fibrillar network deformation, fibril alignment, and cell contact guidance. , 1997, Journal of biomechanical engineering.

[11]  C. le Grimellec,et al.  Imaging of the surface of living cells by low-force contact-mode atomic force microscopy. , 1998, Biophysical journal.

[12]  J. P. Robinson,et al.  Time-lapse confocal reflection microscopy of collagen fibrillogenesis and extracellular matrix assembly in vitro. , 2000, Biopolymers.

[13]  Y Lanir,et al.  A structural theory for the homogeneous biaxial stress-strain relationships in flat collagenous tissues. , 1979, Journal of biomechanics.

[14]  M Eastwood,et al.  Effect of precise mechanical loading on fibroblast populated collagen lattices: morphological changes. , 1998, Cell motility and the cytoskeleton.

[15]  J W Covell,et al.  Functional implications of myocardial scar structure. , 1997, The American journal of physiology.

[16]  F. Yin,et al.  A multiaxial constitutive law for mammalian left ventricular myocardium in steady-state barium contracture or tetanus. , 1998, Journal of biomechanical engineering.

[17]  A. McCulloch,et al.  Modelling cardiac mechanical properties in three dimensions , 2001, Philosophical Transactions of the Royal Society of London. Series A: Mathematical, Physical and Engineering Sciences.

[18]  T. Borg,et al.  Isotonic biaxial loading of fibroblast-populated collagen gels: a versatile, low-cost system for the study of mechanobiology , 2002, Biomechanics and modeling in mechanobiology.

[19]  T. Borg,et al.  Regulation of cardiac myocyte protein turnover and myofibrillar structure in vitro by specific directions of stretch. , 1999, Circulation research.

[20]  R T Tranquillo,et al.  A finite element solution for the anisotropic biphasic theory of tissue-equivalent mechanics: the effect of contact guidance on isometric cell traction measurement. , 1997, Journal of biomechanical engineering.

[21]  R. Lal,et al.  Biological applications of atomic force microscopy. , 1994, The American journal of physiology.

[22]  M Eastwood,et al.  Molecular responses of human dermal fibroblasts to dual cues: contact guidance and mechanical load. , 2000, Cell motility and the cytoskeleton.

[23]  J. Lévêque,et al.  Measurement of mechanical forces generated by skin fibroblasts embedded in a three-dimensional collagen gel. , 1991, The Journal of investigative dermatology.

[24]  V. Fast,et al.  Anisotropic activation spread in heart cell monolayers assessed by high-resolution optical mapping. Role of tissue discontinuities. , 1996, Circulation research.

[25]  A D McCulloch,et al.  Automated measurement of myofiber disarray in transgenic mice with ventricular expression of ras , 1998, The Anatomical record.

[26]  Y. Fung Foundations of solid mechanics , 1965 .

[27]  E. Batschelet Circular statistics in biology , 1981 .

[28]  M. Sacks,et al.  Biaxial mechanical properties of the native and glutaraldehyde-treated aortic valve cusp: Part II--A structural constitutive model. , 2000, Journal of biomechanical engineering.

[29]  W D Spotnitz,et al.  Cellular basis for volume related wall thickness changes in the rat left ventricle. , 1974, Journal of molecular and cellular cardiology.

[30]  Y. Lanir Constitutive equations for fibrous connective tissues. , 1983, Journal of biomechanics.