Literature DB >> 264124

Morphometry of the renal corpuscle during normal postnatal growth and compensatory hypertrophy. A light microscope study.

G Olivetti, P Anversa, W Rigamonti, L Vitali-Mazza, A V Loud.   

Abstract

Renal corpuscles from the juxtamedullary and subcapsular regions of the renal cortex were morphometrically analyzed in young rats and in adult rats that had been unilaterally nephrectomized or sham-operated at an early age. Mean corpuscular volumes increased 4.5-fold during normal development, and 7.7-fold as a result of compensatory hypertrophy in both cortical regions. Relative and absolute volumes were determined for Bowman's space, the glomerular tuft, and five glomerular components: epithelial, endothelial, and mesangial cells, capillaries, and the filtration membrane. Normal and hypertrophic enlargement of Bowman's space was slightly greater than glomerular growth, and the growth response of subcapsular glomeruli was greater than that of juxtamedullary glomeruli. The ratio of mean glomerular volumes between outer and inner glomeruli was 1:2 in both adult groups. Both adult groups also developed nearly identical proportions of all glomerular component structures, representing a relative decrease of epithelial cells and increase of capillaries compared to the young animals. Normal and hypertrophic maturation involved absolute increases in all glomerular cell populations, the length of capillary loops and the surface area of the filtration membrane, all nearly in proportion to the respective four- and seven-fold increases in glomerular volume. Changes in the filtration surface area are consistent with published data for glomerular filtration rates in normal and hypertrophied kidneys. The mean cell size in epithelial and mesangial populations doubled during growth, but was not greater than normal in mononephrectomized rats. Hyperplasia among all populations of glomerular cells is indicated in normal growth, and to a greater extent in compensatory renal hypertrophy.

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Year:  1977        PMID: 264124      PMCID: PMC2109942          DOI: 10.1083/jcb.75.2.573

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  24 in total

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Authors:  R L Jamison
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2.  Alterations in renal and plasma amino acid concentrations during renal compensatory growth.

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3.  Dynamics of glomerular ultrafiltration in the rat. II. Plasma-flow dependence of GFR.

Authors:  B M Brenner; J L Troy; T M Daugharty; W M Deen; C R Robertson
Journal:  Am J Physiol       Date:  1972-11

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Authors:  K Kawano; J Wenzl; J McCoy; J Porch; P Kimmelstiel
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5.  Nucleic acids in compensatory renal hypertrophy.

Authors:  N B Kurnick; P A Lindsay
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6.  Regional variation in capillary permeability of ventricular myocardium.

Authors:  P Anversa; F Giacomelli; J Wiener
Journal:  Microvasc Res       Date:  1973-11       Impact factor: 3.514

7.  Compensatory renal growth after unilateral nephrectomy in the new-born rat.

Authors:  S E Dicker; D G Shirley
Journal:  J Physiol       Date:  1973-01       Impact factor: 5.182

8.  ostnatal development of renal function: micropuncture and clearance studies in the dog.

Authors:  M Horster; H Valtin
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9.  Renal function immediately after contralateral nephrectomy: relation to the mechanism of compensatory kidney growth.

Authors:  A I Katz
Journal:  Yale J Biol Med       Date:  1970-12

10.  A quantitative stereological description of the ultrastructure of normal rat liver parenchymal cells.

Authors:  A V Loud
Journal:  J Cell Biol       Date:  1968-04       Impact factor: 10.539

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  17 in total

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Authors:  L S Young; M C Regan; M K Barry; J G Geraghty; J M Fitzpatrick
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Review 2.  Regional renal blood flow in normal and disease states.

Authors:  M C Regan; L S Young; J Geraghty; J M Fitzpatrick
Journal:  Urol Res       Date:  1995

3.  Renal hypertrophy in experimental diabetes. A morphometric study.

Authors:  K Seyer-Hansen; J Hansen; H J Gundersen
Journal:  Diabetologia       Date:  1980-06       Impact factor: 10.122

4.  Establishment of conditionally immortalized human glomerular mesangial cells in culture, with unique migratory properties.

Authors:  Ramadan M Sarrab; Rachel Lennon; Lan Ni; Matthew D Wherlock; Gavin I Welsh; Moin A Saleem
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5.  Proliferation and remodeling of the peritubular microcirculation after nephron reduction: association with the progression of renal lesions.

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Journal:  Am J Pathol       Date:  2001-08       Impact factor: 4.307

6.  JunD protects against chronic kidney disease by regulating paracrine mitogens.

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7.  Pharmacological characterization of the P2 receptors profile in the podocytes of the freshly isolated rat glomeruli.

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8.  Structural-functional relationships in diabetic nephropathy.

Authors:  S M Mauer; M W Steffes; E N Ellis; D E Sutherland; D M Brown; F C Goetz
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9.  Intraglomerular pressure and mesangial stretching stimulate extracellular matrix formation in the rat.

Authors:  B L Riser; P Cortes; X Zhao; J Bernstein; F Dumler; R G Narins
Journal:  J Clin Invest       Date:  1992-11       Impact factor: 14.808

10.  Role of mesangial cell contraction in adaptation of the glomerular tuft to changes in extracellular volume.

Authors:  M Elger; T Sakai; W Kriz
Journal:  Pflugers Arch       Date:  1990-02       Impact factor: 3.657

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