Cerebral endothelial cell infection by measles virus in subacute sclerosing panencephalitis: ultrastructural and in situ hybridization evidence

1991 ◽  
Vol 17 (4) ◽  
pp. 289-297 ◽  
Author(s):  
J. KIRK ◽  
A. L. ZHOU ◽  
S. McQUAID ◽  
S. L. COSBY ◽  
D I. V. ALLEN
Neurology ◽  
1985 ◽  
Vol 35 (11) ◽  
pp. 1605-1605 ◽  
Author(s):  
P. Shapshak ◽  
W. W. Tourtellotte ◽  
S. Nakamura ◽  
M. C. Graves ◽  
M. Darvish ◽  
...  

Blood ◽  
1996 ◽  
Vol 87 (1) ◽  
pp. 174-179 ◽  
Author(s):  
MA Courtney ◽  
PJ Haidaris ◽  
VJ Marder ◽  
LA Sporn

Abstract Tissue factor (TF) mRNA expression was measured by in situ hybridization in the endothelium of the intact human umbilical vein after infection with Rickettsia rickettsii. At 4 hours, R rickettsii organisms were clearly visible within approximately 70% of endothelial cells by immunocytochemical staining. Quantitation of TF mRNA expression revealed that the level within endothelial cells of the infected vein was significantly greater (3.7-fold, P < .0001) than that detected in uninfected endothelial cells. Serial sections of the umbilical cord vein were processed for in situ hybridization, and immunocytochemical staining and showed TF expression in those endothelial cells that contained R rickettsii organisms. Immunocytochemical staining for TF antigen at 6 hours was negative, but TF was clearly demonstrated within macrophages and fibroblasts of both control and infected umbilical cords. These studies demonstrate that the vascular endothelial cell, ex vivo, can be directly induced to express TF mRNA. This observation has not heretofore been clearly demonstrated except for in cultured endothelial cells. Since R rickettsii infection induces thrombotic vascular occlusions in patients with Rocky Mountain Spotted Fever, the results imply a potential role for endothelial cell TF in the pathogenesis of thrombotic disease.


2000 ◽  
Vol 74 (3) ◽  
pp. 1533-1537 ◽  
Author(s):  
Gregory P. Owens ◽  
R. Anthony Williamson ◽  
Mark P. Burgoon ◽  
Omar Ghausi ◽  
Dennis R. Burton ◽  
...  

ABSTRACT In central nervous system (CNS) infectious and inflammatory diseases of known cause, oligoclonal bands represent antibody directed against the causative agent. To determine whether disease-relevant antibodies can be cloned from diseased brain, we prepared an antibody phage display library from the brain of a human with subacute sclerosing panencephalitis (SSPE), a chronic encephalitis caused by measles virus, and selected the library against SSPE brain sections. Antibodies that were retrieved reacted strongly with measles virus cell extracts by enzyme-linked immunosorbent assay and were specific for the measles virus nucleocapsid protein. These antibodies immunostained cells in different SSPE brains but not in control brain. Our data provide the first demonstration that diseased brain can be used to select in situ for antibodies directed against the causative agent of disease and point to the potential usefulness of this approach in identifying relevant antibodies in chronic CNS or systemic inflammatory diseases of unknown cause.


1999 ◽  
Vol 80 (9) ◽  
pp. 2393-2397 ◽  
Author(s):  
J. Lindsay Oaks ◽  
Catherine Ulibarri ◽  
Timothy B. Crawford

Equine infectious anaemia virus (EIAV) infection of horses is characterized clinically by recurrent episodes of fever, thrombocytopenia and anaemia. In vivo, the only site of virus replication that has been previously demonstrated for EIAV is the tissue macrophage. In this study, in situ hybridization for EIAV was combined with immunohistochemistry for cell-type-specific markers to identify infected endothelial cells. EIAV-infected endothelial cells and macrophages were detected in horses infected with either virulent wild-type or with weakly virulent tissue culture-adapted strains of EIAV. The role of endothelial cell infection in the pathogenesis of EIAV remains undefined, but could contribute to the development of thrombocytopenia. However, endothelial cell infection does not appear to be a determinant of virulence for EIAV.


2007 ◽  
Vol 120 (10) ◽  
pp. 859-862 ◽  
Author(s):  
Hong-wei BAI ◽  
Bing-yi SHI ◽  
Ye-yong QIAN ◽  
Yan-qun NA ◽  
Xuan ZENG ◽  
...  

1986 ◽  
Vol 67 (5) ◽  
pp. 907-913 ◽  
Author(s):  
M. F. Basle ◽  
J. G. Fournier ◽  
S. Rozenblatt ◽  
A. Rebel ◽  
M. Bouteille

1997 ◽  
Vol 3 (S2) ◽  
pp. 35-36
Author(s):  
LF. Brown ◽  
H.F. Dvorak

The formation of vascular stroma (angiogenesis) is essential for tumor growth and may also influence invasion and metastasis. Quantitation of angiogenesis may serve as a prognostic marker in certain malignancies and novel therapies targeted at inhibiting angiogenesis may prove to play an important role in control of tumor growth.In situ hybridization (ISH) studies have helped to define some of the molecular and cellular events responsible for the formation of vascular stroma in malignancy.Vascular permeability factor (VPF), also known as vascular endothelial growth factor (VEGF), is a multifunctional cytokine associated with tumor angiogenesis. Vascular endothelial cells express at least two tyrosine kinase receptors for VPF, flt-1 and KDR. VPF acts as an angiogenic factor in several ways. It is an endothelial cell growth factor, alters endothelial cell gene expression, induces endothelial cell migration, and it is also a potent inducer of microvascular hyperpermeability (50,000 times as strong as histamine).


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