The liver sinusoidal endothelial cell: a cell type of controversial and confusing identity

2008 ◽  
Vol 294 (2) ◽  
pp. G391-G400 ◽  
Author(s):  
Kjetil Elvevold ◽  
Bård Smedsrød ◽  
Inigo Martinez

A look through the literature on liver sinusoidal endothelial cells (LSECs) reveals that there are several conflicts among different authors of what this cell type is and does. Major controversies that will be highlighted in this review include aspects of the physiological role, the characterization, and the protocols of isolation and cultivation of these cells. Many of these conflicts may be ascribed to the fact that the cell was only recently established as a distinct cell type and that researchers from different disciplines tend to define their structure and function differently. This field is in need of a common platform to obtain a sound communication and a unified understanding of how to interpret novel research results. The aim of this review is to encourage scientists not to ignore the fact that there are, indeed, different opinions in the literature on LSECs. We also hope that this review will point out to the reader that some issues that may seem well established regarding our knowledge about the LSECs, in reality, are still unresolved and, indeed, controversial.

2017 ◽  
Vol 16 (1) ◽  
Author(s):  
Shahida Saharudin ◽  
Norlelawati A. Talib ◽  
Nor Zamzila Abdullah ◽  
Jamalludin Ab. Rahman ◽  
Zunariah Buyong

Introduction: Liver perfusion has been the standard method to digest and isolate liver cells including liver sinusoidal endothelial cells (LSEC). Poor cannulating skills through portal vein results in a waste of animal resource. Familiarization of both liver perfusion technique and adhering strictly to aseptic technique during cell handling ensure high cell yield, minimum morphology disruption and cell contamination. We aimed to present a method of liver perfusion procedure followed by the isolation of LSEC. Materials and method: The study was conducted with the approval of IACUC committee. Seven Sprague Dawley rats underwent these procedures under anaesthesia. Liver perfusion was done as previously described. Briefly, LSEC were isolated by liberase enzyme perfusion of the liver, isopycnic sedimentation in a two- step Percoll gradient and selective adherence. The purification and cultivation of LSEC was evaluated by light and electron microscopy. Results: Purity and viability of LSEC after selective adherence was 80.5 ± 3.5% and ≥ 95 %, respectively. The average concentration of the cells ranged from 32 - 75 x 106 per 400 gm rat. After 8 hours of culture, LSEC monolayers were contaminated with less than 5% of other cells. Conclusion: This method is reliable and reproducible for the isolation of LSEC to enable the study of structure and function of these cells in vitro. However, improvement on the perfusion skills and isolation technique are vital to ensure better cell purity.


Life Sciences ◽  
1981 ◽  
Vol 28 (13) ◽  
pp. 1425-1438 ◽  
Author(s):  
William J. Bettger ◽  
Boyd L. O'Dell

Author(s):  
Mark Lorch

This chapter examines proteins, the dominant proportion of cellular machinery, and the relationship between protein structure and function. The multitude of biological processes needed to keep cells functioning are managed in the organism or cell by a massive cohort of proteins, together known as the proteome. The twenty amino acids that make up the bulk of proteins produce the vast array of protein structures. However, amino acids alone do not provide quite enough chemical variety to complete all of the biochemical activity of a cell, so the chapter also explores post-translation modifications. It finishes by looking as some dynamic aspects of proteins, including enzyme kinetics and the protein folding problem.


1999 ◽  
Vol 274 (40) ◽  
pp. 28697-28707 ◽  
Author(s):  
Robert M. Tjin Tham Sjin ◽  
Kenneth A. Lord ◽  
Abbas Abdollahi ◽  
Barbara Hoffman ◽  
Dan A. Liebermann

2008 ◽  
Vol 7 (1) ◽  
Author(s):  
Inigo Martinez ◽  
Geir I Nedredal ◽  
Cristina I Øie ◽  
Alessandra Warren ◽  
Oddmund Johansen ◽  
...  

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