scholarly journals 3D Imaging of Dendritic Cells Using Serial Ion-Abrasion Scanning Electron Microscopy (SIASEM) Reveals That HIV-1 is Stored Within Surface-connected Membrane Folds

2010 ◽  
Vol 16 (S2) ◽  
pp. 1098-1099
Author(s):  
N Avishai ◽  
A Avishai ◽  
H Yu ◽  
M Hitomi ◽  
A Heuer ◽  
...  

Extended abstract of a paper presented at Microscopy and Microanalysis 2010 in Portland, Oregon, USA, August 1 – August 5, 2010.

Blood ◽  
2011 ◽  
Vol 118 (18) ◽  
pp. 4841-4852 ◽  
Author(s):  
Damjan S. Nikolic ◽  
Martin Lehmann ◽  
Richard Felts ◽  
Eduardo Garcia ◽  
Fabien P. Blanchet ◽  
...  

AbstractHIV-1 cell-to-cell transmission confers a strong advantage as it increases efficiency of transfer up to 100-fold compared with a cell-free route. Mechanisms of HIV-1 cell-to-cell transmission are still unclear and can in part be explained by the presence of actin-containing cellular protrusions. Such protrusions have been shown to facilitate cell-to-cell viral dissemination. Using fluorescence microscopy, electron tomography, and ion abrasion scanning electron microscopy we show that HIV-1 induces membrane extensions in immature dendritic cells through activation of Cdc42. We demonstrate that these extensions are induced after engagement of DC-SIGN by HIV-1env via a cascade that involves Src kinases, Cdc42, Pak1, and Wasp. Silencing of Cdc42 or treatment with a specific Cdc42 inhibitor, Secramine A, dramatically reduced the number of membrane protrusions visualized on the cell surface and decreased HIV-1 transfer via infectious synapses. Ion abrasion scanning electron microscopy of cell-cell contact regions showed that cellular extensions from immature dendritic cells that have the appearance of thin filopodia in thin section images are indeed extended membranous sheets with a narrow cross section. Our results demonstrate that HIV-1 binding on immature dendritic cells enhances the formation of membrane extensions that facilitate HIV-1 transfer to CD4+ T lymphocytes.


2016 ◽  
Vol 163 ◽  
pp. 6-18 ◽  
Author(s):  
Teruo Hashimoto ◽  
George E. Thompson ◽  
Xiaorong Zhou ◽  
Philip J. Withers

2008 ◽  
Vol 14 (S2) ◽  
pp. 972-973
Author(s):  
M Hildebrand ◽  
S Kim ◽  
D Shi ◽  
S Subramaniam

Extended abstract of a paper presented at Microscopy and Microanalysis 2008 in Albuquerque, New Mexico, USA, August 3 – August 7, 2008


Author(s):  
Kan Kobayashi

It is known that some kinds of dendritic cells are distributed in the epithelial cell layer of mucous membrane consisting of stratified squamous epithelium. In the process of exfoliation of the epithelial layer from the underlying connective tissue, dendritic cell bodies exposed on the ruptured surface of the epithelium were detected by scanning electron microscopy. These cells were also observed by light microscopy as well as by transmission electron microscopy.Dorsal mucous membrane of the ox tongue was fixed in Karnovsky's fixative or in 10% formalin. For scanning electron microscopy samples were immersed in 3N-HCl solution for 2-3 weeks at room temperature. The epithelial cell layer was removed from the underlying connective tissue layer1). They were postfixed in tannic acid and then 1% OsO4 for 1 hr. After dehydration in an ethanol series, the specimens were dried by passing through t-butylalcohol, coated with platinum-palladium and observed under an S-800 scanning electron microscope. For transmission electron microscopy, small pieces of the fixed tissue were post-fixed in 1% OsO4 for 1.5 hr and then embedded in Araldite-Epon.


2009 ◽  
Vol 166 (3) ◽  
pp. 316-328 ◽  
Author(s):  
Mark Hildebrand ◽  
Sang Kim ◽  
Dan Shi ◽  
Keana Scott ◽  
Sriram Subramaniam

Placenta ◽  
2017 ◽  
Vol 59 ◽  
pp. 175-176
Author(s):  
Haruhiko Shimada ◽  
Yuuki Yamaguchi ◽  
Takami Takizawa ◽  
Hironori Takahashi ◽  
Akihid Ohkuchi ◽  
...  

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