|
|
|
||||
| Home Help Feedback Subscriptions Archive Search Table of Contents | |||||
Journal of Cell Science, Vol 90, Issue 1 145-156, Copyright © 1988 by Company of Biologists
JOURNAL ARTICLES |
SJ Green, G Tarone and CB Underhill
Department of Anatomy and Cell Biology, Georgetown University Medical Center, Washington, DC 20007.
In the present study, we have examined the distribution of both hyaluronate receptors and hyaluronate in adult hamster lung. The receptor for hyaluronate is a transmembrane glycoprotein of Mr 85,000 that interacts with actin filaments and is thought to mediate many of the effects that hyaluronate has on cell behaviour, such as cell-to-cell adhesion and migration. It was localized histochemically with a monoclonal antibody, designated as K-3, which specifically binds to the receptor. Hyaluronate was detected by a biotinylated form of cartilage proteoglycan, which binds with high affinity and specificity to hyaluronate. At the light-microscopic level, both hyaluronate and its receptor were present on the basolateral surfaces of bronchial and bronchiolar epithelium, suggesting that these two components interact with each other. This interaction may be important for maintaining the attachment of the epithelium to the basement membrane. In addition, hyaluronate was present in the adventitial regions of large pulmonary blood vessels. Receptors for hyaluronate were also evident on the surfaces of pulmonary macrophages, as demonstrated by the fact that K-3 immunoreactive cells coincided with cells positive for non-specific esterase, a characteristic feature of macrophages. The receptors on pulmonary macrophages probably mediate the effects that hyaluronate has on these cells with respect to cell-to-cell adhesion and migration.
This article has been cited by other articles:
![]() |
N. Borg and M. Holland The effect of glycosaminoglycans on rat gametes in vitro and the associated signal pathway Reproduction, March 1, 2008; 135(3): 311 - 319. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. D. Kenagy, J. W. Fischer, S. Lara, J. D. Sandy, A. W. Clowes, and T. N. Wight Accumulation and Loss of Extracellular Matrix During Shear Stress-mediated Intimal Growth and Regression in Baboon Vascular Grafts J. Histochem. Cytochem., January 1, 2005; 53(1): 131 - 140. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Nandi, P. Estess, and M. H. Siegelman Hyaluronan Anchoring and Regulation on the Surface of Vascular Endothelial Cells Is Mediated through the Functionally Active Form of CD44 J. Biol. Chem., May 12, 2000; 275(20): 14939 - 14948. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Estess, A. Nandi, M. Mohamadzadeh, and M. H. Siegelman Interleukin 15 Induces Endothelial Hyaluronan Expression In Vitro and Promotes Activated T Cell Extravasation through a CD44-dependent Pathway In Vivo J. Exp. Med., July 5, 1999; 190(1): 9 - 20. [Abstract] [Full Text] [PDF] |
||||
![]() |
Q. Yu, B. P. Toole, and I. Stamenkovic Induction of Apoptosis of Metastatic Mammary Carcinoma Cells In Vivo by Disruption of Tumor Cell Surface CD44 Function J. Exp. Med., December 15, 1997; 186(12): 1985 - 1996. [Abstract] [Full Text] [PDF] |
||||
![]() |
P Pavasant, T Shizari, and C. Underhill Hyaluronan contributes to the enlargement of hypertrophic lacunae in the growth plate J. Cell Sci., January 2, 1996; 109(2): 327 - 334. [Abstract] [PDF] |
||||
![]() |
S. Neame, C. Uff, H Sheikh, S. Wheatley, and C. Isacke CD44 exhibits a cell type dependent interaction with triton X-100 insoluble, lipid rich, plasma membrane domains J. Cell Sci., January 9, 1995; 108(9): 3127 - 3135. [Abstract] [PDF] |
||||