help button home button Am J Pathol ASIP MEMBERSHIP
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Order Full text via Infotrieve
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sterzel, R. B.
Right arrow Articles by Kashgarian, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sterzel, R. B.
Right arrow Articles by Kashgarian, M.

American Journal of Pathology, Vol 125, 130-140, Copyright © 1986 by American Society for Investigative Pathology


REGULAR ARTICLES

Mesangial cell hillocks. Nodular foci of exaggerated growth of cells and matrix in prolonged culture

RB Sterzel, DH Lovett, HG Foellmer, M Perfetto, D Biemesderfer and M Kashgarian

To examine the capability of glomerular mesangial cells (MCs) to produce extracellular matrix, the authors studied MCs in culture by light and electron microscopy as well as immunocytochemistry. MCs were obtained from isolated rat glomeruli and maintained up to 12 weeks in medium containing 20% fetal calf serum. MC outgrowth of primary culture and of up to three subcultures showed characteristic organization consisting of bands of elongated or stellate intertwined cells. After confluency at 10-16 days, MCs continued to grow in irregular multilayers. MCs produced extracellular matrix material within 2-4 days after plating, and large amounts of matrix accumulated with time. By 2- 3 weeks, foci of exaggerated MC proliferation, matrix secretion, and necrotic cell debris formed nodular protrusions, which gradually produced large hillocks. Immunocytochemical studies of MC outgrowths were performed on culture plates or on sectioned material with the use of specific rabbit polyclonal antibodies to isolated matrix proteins and FITC-conjugated, affinity-purified second antibodies. Within 3 days of culture, MCs elaborated fibronectin and collagen Types I, III, IV, and V. With time, strands of matrix, notably in the central mass of hillocks, stained extensively for these constituents. Staining for laminin was less pronounced. Smooth muscle cell myosin was regularly found on distinct intracellular fibrils and in the extracellular material of hillocks. Electron microscopy revealed the hillocks to be composed of elongated cells on the surface and stellate cells intermingled with matrix and necrotic cell debris in the core. The results show that proliferating MCs can be maintained in homogeneous culture for a prolonged time period. MCs produce large amounts of the extracellular matrix proteins (Type IV and V collagen, fibronectin, laminin), which are found in normal glomeruli. Cultured MCs also produce interstitial collagen Types I and III. MC hillocks show the nodular accumulation of matrix similar to that seen in the mesangium of diseased glomeruli. It is concluded that the in vitro model of prolonged MC outgrowth may facilitate the investigation of factors that govern mesangial matrix production. Such a model could be used in examining the response of the mesangium to defined inflammatory or metabolic stimuli.


This article has been cited by other articles:


Home page
Am. J. Physiol. Renal Physiol.Home page
Q. Xu, J. T. Norman, S. Shrivastav, J. Lucio-Cazana, and J. B. Kopp
In vitro models of TGF-beta-induced fibrosis suitable for high-throughput screening of antifibrotic agents
Am J Physiol Renal Physiol, August 1, 2007; 293(2): F631 - F640.
[Abstract] [Full Text] [PDF]


Home page
Nephrol Dial TransplantHome page
J. Rincon, N. T. Viera, M. J. Romero, and J. A. Mosquera
Increased production of chemotactic cytokines and elevated proliferation and expression of intercellular adhesion molecule-1 in rat mesangial cells treated with erythrogenic toxin type B and its precursor isolated from nephritogenic streptococci
Nephrol. Dial. Transplant., June 1, 2003; 18(6): 1072 - 1078.
[Abstract] [Full Text] [PDF]


Home page
Nephrol Dial TransplantHome page
P. Mene, C. Caenazzo, F. Pugliese, G. A. Cinotti, A. D'Angelo, S. Garbisa, and G. Gambaro
Monocyte/mesangial cell interactions in high-glucose co-cultures
Nephrol. Dial. Transplant., May 1, 2001; 16(5): 913 - 922.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Renal Physiol.Home page
F. Amiri and R. Garcia
Regulation of angiotensin II receptors and PKC isoforms by glucose in rat mesangial cells
Am J Physiol Renal Physiol, May 1, 1999; 276(5): F691 - F699.
[Abstract] [Full Text] [PDF]


Home page
J. Am. Soc. Nephrol.Home page
M. KITAMURA
The Antioxidant N-Acetylcysteine Induces Mesangial Cells to Create Three-Dimensional Cytoarchitecture That Underlies Cellular Differentiation
J. Am. Soc. Nephrol., April 1, 1999; 10(4): 746 - 751.
[Abstract] [Full Text]


Home page
HypertensionHome page
P. R. Mertens, V. Espenkott, B. Venjakob, B. Heintz, S. Handt, and H.-G. Sieberth
Pressure Oscillation Regulates Human Mesangial Cell Growth and Collagen Synthesis
Hypertension, November 1, 1998; 32(5): 945 - 952.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1986 by the American Society for Investigative Pathology.