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1.
Am J Physiol Renal Physiol ; 293(6): F1787-98, 2007 Dec.
Article in English | MEDLINE | ID: mdl-17715264

ABSTRACT

Production of urine is initiated by fluid and solute flux across the glomerular filtration barrier. Recent ultrastructural studies have shown that under extreme conditions of no filtration, or very high filtration, a restriction to flow is predicted in a space underneath the podocyte cell body or its processes, the subpodocyte space (SPS). The SPS covered up to two-thirds of the glomerular filtration barrier (GFB) surface. The magnitude of this restriction to flow suggested that it might be unlikely that filtration into and flow through the SPS would contribute significantly to total flow across the entire GFB under these conditions. To determine whether the SPS has similar properties under normal physiological conditions, we have carried out further three-dimensional reconstruction of rat glomeruli perfused at physiologically normal hydrostatic and colloid osmotic pressures. These reconstructions show that the sub-podocyte space is even more restricted under these conditions, with a mean height of the SPS of 0.34 microm, mean pathlength of 6.7 +/- 1.4 mum, a mean width of the SPS exit pore of 0.15 +/- 0.05 microm, and length of 0.25 +/- 0.05 microm. Mathematical modeling of this SPS based on a circular flow model predicts that the resistance of these dimensions is 2.47 times that of the glomerular filtration barrier and exquisitely sensitive to changes in the dimensions of the SPS exit pore (SEP), indicating that the SEP could be the principal regulator of the extravascular pressure in the SPS. This suggests a physiological role of the podocyte in the regulation of glomerular fluid flux across most of the GFB.


Subject(s)
Kidney Glomerulus/physiology , Kidney/metabolism , Podocytes/physiology , Algorithms , Animals , Colloids , Glomerular Filtration Rate , Image Processing, Computer-Assisted , In Vitro Techniques , Kidney/cytology , Kidney/ultrastructure , Kidney Glomerulus/cytology , Kidney Glomerulus/metabolism , Models, Statistical , Osmotic Pressure , Perfusion , Podocytes/ultrastructure , Rats , Rats, Inbred WKY
2.
Am J Physiol Renal Physiol ; 293(6): F1777-86, 2007 Dec.
Article in English | MEDLINE | ID: mdl-17804486

ABSTRACT

The glomerular filtration barrier (GFB) is generally considered to consist of three layers: fenestrated glomerular endothelium, glomerular basement membrane, and filtration slits between adjacent podocyte foot processes. Detailed anatomic examination of the GFB has revealed a novel abluminal structure, the subpodocyte space (SPS), identified as the labyrinthine space between the underside of podocyte cell body/primary processes and the foot processes. The SPS covers 50-65% of the filtration surface of the GFB, indicating that SPS may influence glomerular permeability. We have examined the contribution of the SPS to the permeability characteristics of the GFB using multiphoton microscopy techniques in isolated, perfused glomeruli and in the intact kidney in vivo. SPS were identified using this technique, with comparable dimensions to SPS examined with electron microscopy. The passage of the intermediate-weight molecule rhodamine-conjugated 10-kDa dextran, but not the low-weight molecule lucifer yellow ( approximately 450 Da), accumulated in SPS-covered regions of the GFB, compared with GFB regions not covered by SPS ("naked regions"). Net lucifer yellow flux (taken to indicate fluid flux) through identifiable SPS regions was calculated to be 66-75% of that occurring through naked regions. These observations indicate both ultrafiltration and hydraulic resistance imparted by the SPS, demonstrating the potential physiological contribution of the SPS to glomerular permeability.


Subject(s)
Capillary Permeability/physiology , Kidney Glomerulus/metabolism , Podocytes/metabolism , Animals , Basement Membrane/metabolism , Body Fluids/metabolism , Capillaries/metabolism , Coloring Agents , Dextrans , Female , Fluorescent Dyes , Image Processing, Computer-Assisted , In Vitro Techniques , Isoquinolines , Kidney Glomerulus/cytology , Male , Microscopy, Confocal , Microscopy, Fluorescence , Microscopy, Fluorescence, Multiphoton , Perfusion , Rabbits , Rats , Rats, Wistar , Rhodamines
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