help button home button Am J Pathol R & D Systems
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 Yaoita, E.
Right arrow Articles by Kihara, I.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Yaoita, E.
Right arrow Articles by Kihara, I.

American Journal of Pathology, Vol 149, 319-327, Copyright © 1996 by American Society for Investigative Pathology


REGULAR ARTICLES

Perinuclear distribution of plectin characterizes visceral epithelial cells of rat glomeruli

E Yaoita, G Wiche, T Yamamoto, K Kawasaki and I Kihara
Department of Pathology, Institute of Nephrology, Niigata University School of Medicine, Japan.

Plectin is an intermediate-filament-associated protein identified over a wide range of tissue and cell types. The distribution of this protein in glomerular visceral epithelial cells (VECs) during the differentiation and growth of rat kidneys was studied in comparison with that of vimentin. By immunofluorescence microscopy, preferential localization of these two cytomatrix elements was different, although both were observed in the cell body and primary processes of VECs. Strong staining of plectin was always found in the perinuclear region of the VEC body in kidneys of young and adult rat, but vimentin stained distinctly only in the primary processes of young rats yet in both cell bodies and primary processes of the adults. This perinuclear staining was unique to VECs, that is, was absent from other cells. In the neonatal kidney, plectin staining during differentiation of VECs changed from weak and diffuse throughout the cytoplasm in the S-shaped body to prominently perinuclear in the maturing stage. However, after the differentiation of VECs, the staining intensity of plectin did not change further. In contrast, that of vimentin increased conspicuously in parallel with the growth of VECs rather than at differentiation. After a long period of culture and during aminonucleoside nephrosis, situations when VECs lose differentiated phenotypes, most of the cells had no perinuclear plectin. These findings indicate that the perinuclear distribution of plectin may play an important role in the differentiation of VECs.


This article has been cited by other articles:


Home page
Physiol. Rev.Home page
H. Pavenstadt, W. Kriz, and M. Kretzler
Cell Biology of the Glomerular Podocyte
Physiol Rev, January 1, 2003; 83(1): 253 - 307.
[Abstract] [Full Text] [PDF]


Home page
J. Am. Soc. Nephrol.Home page
D. KONDO, T. YAMAMOTO, E. YAOITA, P. E. DANIELSON, H. KOBAYASHI, K. OHSHIRO, H. FUNAKI, Y. KOYAMA, H. FUJINAKA, K. KAWASAKI, et al.
Localization of Olfactomedin-Related Glycoprotein Isoform (BMZ) in the Golgi Apparatus of Glomerular Podocytes in Rat Kidneys
J. Am. Soc. Nephrol., May 1, 2000; 11(5): 803 - 813.
[Abstract] [Full Text]


Home page
J. Cell Sci.Home page
T Hijikata, T Murakami, M Imamura, N Fujimaki, and H Ishikawa
Plectin is a linker of intermediate filaments to Z-discs in skeletal muscle fibers
J. Cell Sci., January 3, 1999; 112(6): 867 - 876.
[Abstract] [PDF]


Home page
Am. J. Physiol. Renal Physiol.Home page
H. Kurihara, N. Sunagawa, T. Kobayashi, K. Kimura, N. Takasu, and T. Shike
Monoclonal antibody P-31 recognizes a novel intermediate filament-associated protein (p250) in rat podocytes
Am J Physiol Renal Physiol, May 1, 1998; 274(5): F986 - F997.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
G Wiche
Role of plectin in cytoskeleton organization and dynamics
J. Cell Sci., January 9, 1998; 111(17): 2477 - 2486.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1996 by the American Society for Investigative Pathology.