New ways of looking at very small holes - Using optical nanoscopy to visualize liver sinusoidal endothelial cell fenestrations

Cristina I. Øie, Viola Mönkemöller, Wolfgang Hübner, Mark Schüttpelz, Hong Mao, Balpreet S. Ahluwalia, Thomas R Huser, Peter McCourt

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Super-resolution fluorescence microscopy, also known as nanoscopy, has provided us with a glimpse of future impacts on cell biology. Far-field optical nanoscopy allows, for the first time, the study of sub-cellular nanoscale biological structures in living cells, which in the past was limited to electron microscopy (EM) (in fixed/dehydrated) cells or tissues. Nanoscopy has particular utility in the study of "fenestrations" - phospholipid transmembrane nanopores of 50-150 nm in diameter through liver sinusoidal endothelial cells (LSECs) that facilitate the passage of plasma, but (usually) not blood cells, to and from the surrounding hepatocytes. Previously, these fenestrations were only discernible with EM, but now they can be visualized in fixed and living cells using structured illumination microscopy (SIM) and in fixed cells using single molecule localization microscopy (SMLM) techniques such as direct stochastic optical reconstruction microscopy. Importantly, both methods use wet samples, avoiding dehydration artifacts. The use of nanoscopy can be extended to the in vitro study of fenestration dynamics, to address questions such as the following: are they actually dynamic structures, and how do they respond to endogenous and exogenous agents? A logical further extension of these methodologies to liver research (including the liver endothelium) will be their application to liver tissue sections from animal models with different pathological manifestations and ultimately to patient biopsies. This review will cover the current state of the art of the use of nanoscopy in the study of liver endothelium and the liver in general. Potential future applications in cell biology and the clinical implications will be discussed.

Original languageEnglish (US)
JournalUnknown Journal
DOIs
StateAccepted/In press - Jan 10 2018
Externally publishedYes

Fingerprint

Endothelial cells
liver
Liver
Endothelial Cells
Cytology
endothelium
microscopy
Microscopic examination
Cells
Electron microscopy
Endothelium
Cell Biology
Microscopy
electron microscopy
Electron Microscopy
Nanopores
Tissue
blood cells
animal models
Time and Motion Studies

Keywords

  • endothelium
  • fenestration
  • liver
  • optical nanoscopy

ASJC Scopus subject areas

  • Biotechnology
  • Electronic, Optical and Magnetic Materials
  • Atomic and Molecular Physics, and Optics
  • Electrical and Electronic Engineering

Cite this

Øie, C. I., Mönkemöller, V., Hübner, W., Schüttpelz, M., Mao, H., Ahluwalia, B. S., ... McCourt, P. (Accepted/In press). New ways of looking at very small holes - Using optical nanoscopy to visualize liver sinusoidal endothelial cell fenestrations. Unknown Journal. https://doi.org/10.1515/nanoph-2017-0055

New ways of looking at very small holes - Using optical nanoscopy to visualize liver sinusoidal endothelial cell fenestrations. / Øie, Cristina I.; Mönkemöller, Viola; Hübner, Wolfgang; Schüttpelz, Mark; Mao, Hong; Ahluwalia, Balpreet S.; Huser, Thomas R; McCourt, Peter.

In: Unknown Journal, 10.01.2018.

Research output: Contribution to journalArticle

Øie, Cristina I. ; Mönkemöller, Viola ; Hübner, Wolfgang ; Schüttpelz, Mark ; Mao, Hong ; Ahluwalia, Balpreet S. ; Huser, Thomas R ; McCourt, Peter. / New ways of looking at very small holes - Using optical nanoscopy to visualize liver sinusoidal endothelial cell fenestrations. In: Unknown Journal. 2018.
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