Granulocyte colony-stimulating factor increases hepatic sinusoidal perfusion during liver regeneration in mice

Standard

Granulocyte colony-stimulating factor increases hepatic sinusoidal perfusion during liver regeneration in mice. / Sidler, Daniel; Studer, Peter; Küpper, Sebastian; Gloor, Beat; Candinas, Daniel; Haier, Jörg; Inderbitzin, Daniel.

in: J INVEST SURG, Jahrgang 21, Nr. 2, 15.03.2008, S. 57-64.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Sidler, D, Studer, P, Küpper, S, Gloor, B, Candinas, D, Haier, J & Inderbitzin, D 2008, 'Granulocyte colony-stimulating factor increases hepatic sinusoidal perfusion during liver regeneration in mice', J INVEST SURG, Jg. 21, Nr. 2, S. 57-64. https://doi.org/10.1080/08941930701883632

APA

Sidler, D., Studer, P., Küpper, S., Gloor, B., Candinas, D., Haier, J., & Inderbitzin, D. (2008). Granulocyte colony-stimulating factor increases hepatic sinusoidal perfusion during liver regeneration in mice. J INVEST SURG, 21(2), 57-64. https://doi.org/10.1080/08941930701883632

Vancouver

Bibtex

@article{baf6c5ff43204eb0bc19788d49fd8d8e,
title = "Granulocyte colony-stimulating factor increases hepatic sinusoidal perfusion during liver regeneration in mice",
abstract = "Conditioning with granulocyte colony-stimulating factor (G-CSF) promotes liver regeneration in an experimental small-for-size liver remnant mouse model. The mechanisms involved in this extraordinary G-CSF effect are unknown. The aim of this study was to investigate the influence of G-CSF on the hepatic microvasculature in the regenerating liver. The hepatic sinusoidal microvasculature and microarchitecture of the regenerating liver were evaluated by intravital microscopy in mice. Three experimental groups were compared: (1) unoperated unconditioned animals (control; n = 5), (2) animals conditioned with G-CSF 48 h after 60% partial hepatectomy (G-CSF-PH; n = 6), and (3) animals sham conditioned 48 h after 60% PH (sham-PH; n = 6). PH led to hepatocyte hypertrophy and increased hepatic sinusoidal velocity in the sham-PH and G-CSF-PH groups. Increased sinusoidal diameter and increased hepatic blood flow were observed in the G-CSF-PH group compared to the sham-PH and control groups. Furthermore, there was a strong positive correlation between spleen weight and hepatic sinusoidal diameter in the G-CSF-PH group. The increased hepatic blood flow could explain the observed benefit of G-CSF conditioning during liver regeneration. These results elucidate an unexplored aspect of pharmacological modulation of liver regeneration and motivate further experiments.",
keywords = "Animals, Granulocyte Colony-Stimulating Factor, Hepatectomy, Immunohistochemistry, Ki-67 Antigen, Liver, Liver Circulation, Liver Regeneration, Male, Mice, Mice, Inbred BALB C, Microcirculation, Organ Size",
author = "Daniel Sidler and Peter Studer and Sebastian K{\"u}pper and Beat Gloor and Daniel Candinas and J{\"o}rg Haier and Daniel Inderbitzin",
year = "2008",
month = mar,
day = "15",
doi = "10.1080/08941930701883632",
language = "English",
volume = "21",
pages = "57--64",
journal = "J INVEST SURG",
issn = "0894-1939",
publisher = "informa healthcare",
number = "2",

}

RIS

TY - JOUR

T1 - Granulocyte colony-stimulating factor increases hepatic sinusoidal perfusion during liver regeneration in mice

AU - Sidler, Daniel

AU - Studer, Peter

AU - Küpper, Sebastian

AU - Gloor, Beat

AU - Candinas, Daniel

AU - Haier, Jörg

AU - Inderbitzin, Daniel

PY - 2008/3/15

Y1 - 2008/3/15

N2 - Conditioning with granulocyte colony-stimulating factor (G-CSF) promotes liver regeneration in an experimental small-for-size liver remnant mouse model. The mechanisms involved in this extraordinary G-CSF effect are unknown. The aim of this study was to investigate the influence of G-CSF on the hepatic microvasculature in the regenerating liver. The hepatic sinusoidal microvasculature and microarchitecture of the regenerating liver were evaluated by intravital microscopy in mice. Three experimental groups were compared: (1) unoperated unconditioned animals (control; n = 5), (2) animals conditioned with G-CSF 48 h after 60% partial hepatectomy (G-CSF-PH; n = 6), and (3) animals sham conditioned 48 h after 60% PH (sham-PH; n = 6). PH led to hepatocyte hypertrophy and increased hepatic sinusoidal velocity in the sham-PH and G-CSF-PH groups. Increased sinusoidal diameter and increased hepatic blood flow were observed in the G-CSF-PH group compared to the sham-PH and control groups. Furthermore, there was a strong positive correlation between spleen weight and hepatic sinusoidal diameter in the G-CSF-PH group. The increased hepatic blood flow could explain the observed benefit of G-CSF conditioning during liver regeneration. These results elucidate an unexplored aspect of pharmacological modulation of liver regeneration and motivate further experiments.

AB - Conditioning with granulocyte colony-stimulating factor (G-CSF) promotes liver regeneration in an experimental small-for-size liver remnant mouse model. The mechanisms involved in this extraordinary G-CSF effect are unknown. The aim of this study was to investigate the influence of G-CSF on the hepatic microvasculature in the regenerating liver. The hepatic sinusoidal microvasculature and microarchitecture of the regenerating liver were evaluated by intravital microscopy in mice. Three experimental groups were compared: (1) unoperated unconditioned animals (control; n = 5), (2) animals conditioned with G-CSF 48 h after 60% partial hepatectomy (G-CSF-PH; n = 6), and (3) animals sham conditioned 48 h after 60% PH (sham-PH; n = 6). PH led to hepatocyte hypertrophy and increased hepatic sinusoidal velocity in the sham-PH and G-CSF-PH groups. Increased sinusoidal diameter and increased hepatic blood flow were observed in the G-CSF-PH group compared to the sham-PH and control groups. Furthermore, there was a strong positive correlation between spleen weight and hepatic sinusoidal diameter in the G-CSF-PH group. The increased hepatic blood flow could explain the observed benefit of G-CSF conditioning during liver regeneration. These results elucidate an unexplored aspect of pharmacological modulation of liver regeneration and motivate further experiments.

KW - Animals

KW - Granulocyte Colony-Stimulating Factor

KW - Hepatectomy

KW - Immunohistochemistry

KW - Ki-67 Antigen

KW - Liver

KW - Liver Circulation

KW - Liver Regeneration

KW - Male

KW - Mice

KW - Mice, Inbred BALB C

KW - Microcirculation

KW - Organ Size

U2 - 10.1080/08941930701883632

DO - 10.1080/08941930701883632

M3 - SCORING: Journal article

C2 - 18340621

VL - 21

SP - 57

EP - 64

JO - J INVEST SURG

JF - J INVEST SURG

SN - 0894-1939

IS - 2

ER -