Structural determinants of glomerular permselectivity. 1977

H G Rennke, and M A Venkatachalam

Molecular size has been considered in the past to be the major factor in glomerular restriction of macromolecules. Ultrastructural tracer studies have suggested that the restrictive barriers(s) are present in the glomerular basement membrane (GBM), the epithelial filtration slits, or both. Recent morphologic and functional tracer studies have indicated that, in addition to size, molecular charge and possibly shape are important determinants in the ultrafiltration process. Negatively charged macromolecules are restricted by the glomerulus more than neutral molecules, while positively charged macromolecules of similar size are filtered in greater amounts. The elements responsible for this specific restriction of polyanions and facilitated transport of polycations are glycoproteins rich in carboxyl groups (sialic acid, dicarboxylic amino acids), which constitute the endothelial and epithelial cell coats and part of the matrix of the glomerular basement membrane. Ultrastructurally, the polyanionic elements of the GBM are localized in its subendothelial and subepithelial layers; the lamina densa, in contrast, appears more neutral, containing most likely a collagen-like glycoprotein.

UI MeSH Term Description Entries
D007678 Kidney Glomerulus A cluster of convoluted capillaries beginning at each nephric tubule in the kidney and held together by connective tissue. Glomerulus, Kidney
D008854 Microscopy, Electron Microscopy using an electron beam, instead of light, to visualize the sample, thereby allowing much greater magnification. The interactions of ELECTRONS with specimens are used to provide information about the fine structure of that specimen. In TRANSMISSION ELECTRON MICROSCOPY the reactions of the electrons that are transmitted through the specimen are imaged. In SCANNING ELECTRON MICROSCOPY an electron beam falls at a non-normal angle on the specimen and the image is derived from the reactions occurring above the plane of the specimen. Electron Microscopy
D008954 Models, Biological Theoretical representations that simulate the behavior or activity of biological processes or diseases. For disease models in living animals, DISEASE MODELS, ANIMAL is available. Biological models include the use of mathematical equations, computers, and other electronic equipment. Biological Model,Biological Models,Model, Biological,Models, Biologic,Biologic Model,Biologic Models,Model, Biologic
D008968 Molecular Conformation The characteristic three-dimensional shape of a molecule. Molecular Configuration,3D Molecular Structure,Configuration, Molecular,Molecular Structure, Three Dimensional,Three Dimensional Molecular Structure,3D Molecular Structures,Configurations, Molecular,Conformation, Molecular,Conformations, Molecular,Molecular Configurations,Molecular Conformations,Molecular Structure, 3D,Molecular Structures, 3D,Structure, 3D Molecular,Structures, 3D Molecular
D002374 Catalase An oxidoreductase that catalyzes the conversion of HYDROGEN PEROXIDE to water and oxygen. It is present in many animal cells. A deficiency of this enzyme results in ACATALASIA. Catalase A,Catalase T,Manganese Catalase,Mn Catalase
D005293 Ferritins Iron-containing proteins that are widely distributed in animals, plants, and microorganisms. Their major function is to store IRON in a nontoxic bioavailable form. Each ferritin molecule consists of ferric iron in a hollow protein shell (APOFERRITINS) made of 24 subunits of various sequences depending on the species and tissue types. Basic Isoferritin,Ferritin,Isoferritin,Isoferritin, Basic
D005919 Glomerular Filtration Rate The volume of water filtered out of plasma through glomerular capillary walls into Bowman's capsules per unit of time. It is considered to be equivalent to INULIN clearance. Filtration Rate, Glomerular,Filtration Rates, Glomerular,Glomerular Filtration Rates,Rate, Glomerular Filtration,Rates, Glomerular Filtration
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D001485 Basement Membrane A darkly stained mat-like EXTRACELLULAR MATRIX (ECM) that separates cell layers, such as EPITHELIUM from ENDOTHELIUM or a layer of CONNECTIVE TISSUE. The ECM layer that supports an overlying EPITHELIUM or ENDOTHELIUM is called basal lamina. Basement membrane (BM) can be formed by the fusion of either two adjacent basal laminae or a basal lamina with an adjacent reticular lamina of connective tissue. BM, composed mainly of TYPE IV COLLAGEN; glycoprotein LAMININ; and PROTEOGLYCAN, provides barriers as well as channels between interacting cell layers. Basal Lamina,Basement Lamina,Lamina Densa,Lamina Lucida,Lamina Reticularis,Basement Membranes,Densas, Lamina,Lamina, Basal,Lamina, Basement,Lucida, Lamina,Membrane, Basement,Membranes, Basement,Reticularis, Lamina
D046911 Macromolecular Substances Compounds and molecular complexes that consist of very large numbers of atoms and are generally over 500 kDa in size. In biological systems macromolecular substances usually can be visualized using ELECTRON MICROSCOPY and are distinguished from ORGANELLES by the lack of a membrane structure. Macromolecular Complexes,Macromolecular Compounds,Macromolecular Compounds and Complexes,Complexes, Macromolecular,Compounds, Macromolecular,Substances, Macromolecular

Related Publications

H G Rennke, and M A Venkatachalam
October 1977, Kidney international,
H G Rennke, and M A Venkatachalam
February 2004, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association,
H G Rennke, and M A Venkatachalam
January 1990, American journal of nephrology,
H G Rennke, and M A Venkatachalam
January 1983, The Journal of membrane biology,
H G Rennke, and M A Venkatachalam
July 2001, Current opinion in nephrology and hypertension,
H G Rennke, and M A Venkatachalam
October 2001, American journal of physiology. Renal physiology,
H G Rennke, and M A Venkatachalam
January 1994, The American journal of physiology,
H G Rennke, and M A Venkatachalam
January 2005, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie,
H G Rennke, and M A Venkatachalam
December 2009, Minerva urologica e nefrologica = The Italian journal of urology and nephrology,
H G Rennke, and M A Venkatachalam
January 1992, Advances in nephrology from the Necker Hospital,
Copied contents to your clipboard!