Transport of Spherical Particles Through Fibrous Media and a Row of Parallel Cylinders: Applications to Glomerular Filtration

2017 ◽  
Vol 139 (12) ◽  
Author(s):  
Numpong Punyaratabandhu ◽  
Pimkhwan Kongoup ◽  
Panadda Dechadilok ◽  
Pisut Katavetin ◽  
Wannapong Triampo

Viewed in renal physiology as a refined filtration device, the glomerulus filters large volumes of blood plasma while keeping proteins within blood circulation. Effects of macromolecule size and macromolecule hydrodynamic interaction with the nanostructure of the cellular layers of the glomerular capillary wall on the glomerular size selectivity are investigated through a mathematical simulation based on an ultrastructural model. The epithelial slit, a planar arrangement of fibers connecting the epithelial podocytes, is represented as a row of parallel cylinders with nonuniform spacing between adjacent fibers. The mean and standard deviation of gap half-width between its fibers are based on values recently reported from electron microscopy. The glomerular basement membrane (GBM) is represented as a fibrous medium containing fibers of two different sizes: the size of type IV collagens and that of glycosaminoglycans (GAGs). The endothelial cell layer is modeled as a layer full of fenestrae that are much larger than solute size and filled with GAGs. The calculated total sieving coefficient agrees well with the sieving coefficients of ficolls obtained from in vivo urinalysis in humans, whereas the computed glomerular hydraulic permeability also falls within the range estimated from human glomerular filtration rate (GFR). Our result indicates that the endothelial cell layer and GBM significantly contribute to solute and fluid restriction of the glomerular barrier, whereas, based on the structure of the epithelial slit obtained from electron microscopy, the contribution of the epithelial slit could be smaller than previously believed.

The Analyst ◽  
2015 ◽  
Vol 140 (15) ◽  
pp. 5055-5064 ◽  
Author(s):  
Xiaojie Wu ◽  
Molly A. Newbold ◽  
Christy L. Haynes

Herein, a versatile hydrogel scaffold is embedded in a microfluidic platform that supports an endothelial cell layer; this construct is employed to mimic thein vivoneutrophil transendothelial migration process.


1994 ◽  
Vol 74 (2) ◽  
pp. 85-93 ◽  
Author(s):  
Toshiyuki Kaji ◽  
Syouichi Hiraga ◽  
Noriyasu Fujii ◽  
Chika Yamamoto ◽  
Michiko Sakamoto ◽  
...  

2000 ◽  
Vol 6 (S2) ◽  
pp. 854-855
Author(s):  
B. Sternberg-Papahadjopoulos ◽  
K. Hong ◽  
W. Zheng ◽  
D. Papahadjopoulos

Complexes formed during interaction of cationic liposomes with polynucleotides such as DNA (CLDC) self-assemble into a variety of polymorphic structures. They display bilayer (FIG. 1-5) and non-bilayer structures (FIG. 6). We have recorded bilayer structures such as spaghetti/meatball-type structures (FIG. I), map-pins (FIG. 2) spherical particles and invaginated liposomes (FIG. 3, 4) and oligolamellar structures (FIG. 5). The non-bilayer lipid arrangements include honeycombtype structure (Hn, FIG. 6) and cubic phase lipids.We have chosen mainly freeze-fracture electron microscopy (FIG. 1-3, 5,6) but also cryo-electron microscopy (FIG.4) for recording polymorphic structures, and for studying factors and conditions triggering the formation and stabilization of specific structure types. Furthermore, we took microscopically snapshots of the interaction of specific structure types with cultured cells. In order to find out the “active” structure in terms of transfection, we investigated the transfection activity both in vivo and in vitro of CLDC, and studied in parallel their morphology in serum as well as in cell medium.


2008 ◽  
Vol 36 (10) ◽  
pp. 1681-1689 ◽  
Author(s):  
Michael P. Szymanski ◽  
Eleni Metaxa ◽  
Hui Meng ◽  
John Kolega

1994 ◽  
Vol 46 (4-5) ◽  
pp. 307-313 ◽  
Author(s):  
Hisao Yamaguchi ◽  
Masaru Morisada ◽  
Hirokuni Kaku ◽  
Taka-aki Onodera ◽  
Ryu Kurokawa

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