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1.
Biophys J ; 98(3): L1-3, 2010 Feb 03.
Artigo em Inglês | MEDLINE | ID: mdl-20141747

RESUMO

We investigate the dependence of fiber brightness on three-dimensional fiber orientation when imaging biopolymer networks with confocal reflection microscopy (CRM) and confocal fluorescence microscopy (CFM). We compare image data of fluorescently labeled type I collagen networks concurrently acquired using each imaging modality. For CRM, fiber brightness decreases for more vertically oriented fibers, leaving fibers above approximately 50 degrees from the imaging plane entirely undetected. As a result, the three-dimensional network structure appears aligned with the imaging plane. In contrast, CFM data exhibit little variation of fiber brightness with fiber angle, thus revealing an isotropic collagen network. Consequently, we find that CFM detects almost twice as many fibers as are visible with CRM, thereby yielding more complete structural information for three-dimensional fiber networks. We offer a simple explanation that predicts the detected fiber brightness as a function of fiber orientation in CRM.


Assuntos
Microscopia Confocal/instrumentação , Anisotropia , Biopolímeros/química , Colágeno Tipo I/química , Fluorescência , Géis , Imageamento Tridimensional/instrumentação , Imageamento Tridimensional/métodos , Microscopia Confocal/métodos , Rotação , Gravação em Vídeo
2.
Biophys J ; 95(12): 6072-80, 2008 Dec 15.
Artigo em Inglês | MEDLINE | ID: mdl-18835899

RESUMO

We describe a robust method for determining morphological properties of filamentous biopolymer networks, such as collagen or other connective tissue matrices, from confocal microscopy image stacks. Morphological properties including pore size distributions and percolation thresholds are important for transport processes, e.g., particle diffusion or cell migration through the extracellular matrix. The method is applied to fluorescently labeled fiber networks prepared from rat-tail tendon and calf-skin collagen, at concentrations of 1.2, 1.6, and 2.4 mg/ml. The collagen fibers form an entangled and branched network. The medial axes, or skeletons, representing the collagen fibers are extracted from the image stack by threshold intensity segmentation and distance-ordered homotopic thinning. The size of the fluid pores as defined by the radii of largest spheres that fit into the cavities between the collagen fibers is derived from Euclidean distance maps and maximal covering radius transforms of the fluid phase. The size of the largest sphere that can traverse the fluid phase between the collagen fibers across the entire probe, called the percolation threshold, was computed for both horizontal and vertical directions. We demonstrate that by representing the fibers as the medial axis the derived morphological network properties are both robust against changes of the value of the segmentation threshold intensity and robust to problems associated with the point-spread function of the imaging system. We also provide empirical support for a recent claim that the percolation threshold of a fiber network is close to the fiber diameter for which the Euler index of the networks becomes zero.


Assuntos
Biopolímeros/química , Algoritmos , Animais , Biopolímeros/metabolismo , Bovinos , Colágeno/química , Colágeno/metabolismo , Corantes Fluorescentes/metabolismo , Imageamento Tridimensional , Microscopia Confocal , Modelos Moleculares , Conformação Molecular , Porosidade , Ratos
3.
J Microsc ; 232(3): 463-75, 2008 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-19094023

RESUMO

The geometric structure of a biopolymer network impacts its mechanical and biological properties. In this paper, we develop an algorithm for extracting the network architecture of three-dimensional (3d) fluorescently labeled collagen gels, building on the initial work of Wu et al., (2003). Using artificially generated images, the network extraction algorithm is then validated for its ability to reconstruct the correct bulk properties of the network, including fiber length, persistence length, cross-link density, and shear modulus.


Assuntos
Biopolímeros/química , Colágeno/ultraestrutura , Géis/química , Algoritmos , Simulação por Computador
4.
Phys Rev E Stat Nonlin Soft Matter Phys ; 82(5 Pt 1): 051905, 2010 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-21230498

RESUMO

We study the geometry of biopolymer networks and effects of the geometry on bulk mechanical properties. It is shown numerically that the physical network geometry can be quantified statistically and regenerated from its statistical description, so that the regenerated network exhibits the same network mechanics as the physical network in the elastic regime. A collagen-I biopolymer network is used for validation. The method enables parametric studies of the network geometry, whose parameters are often difficult to vary independently in experiments.


Assuntos
Colágeno Tipo I/química , Elasticidade , Modelos Moleculares , Algoritmos , Animais , Fenômenos Biomecânicos , Bovinos , Análise de Elementos Finitos , Conformação Proteica
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