Plasma microRNA profiles in rat models of hepatocellular injury, cholestasis, and steatosis.

MicroRNAs (miRNAs) are small RNA molecules that function to modulate the expression of target genes, playing important roles in a wide range of physiological and pathological processes. The miRNAs in body fluids have received considerable attention as potential biomarkers of various diseases. In thi...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Yu Yamaura, Miki Nakajima, Shingo Takagi, Tatsuki Fukami, Koichi Tsuneyama, Tsuyoshi Yokoi
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2012
Materias:
R
Q
Acceso en línea:https://doaj.org/article/0984a55d289d4135b90de3377be46fc1
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:0984a55d289d4135b90de3377be46fc1
record_format dspace
spelling oai:doaj.org-article:0984a55d289d4135b90de3377be46fc12021-11-18T07:27:49ZPlasma microRNA profiles in rat models of hepatocellular injury, cholestasis, and steatosis.1932-620310.1371/journal.pone.0030250https://doaj.org/article/0984a55d289d4135b90de3377be46fc12012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22363424/?tool=EBIhttps://doaj.org/toc/1932-6203MicroRNAs (miRNAs) are small RNA molecules that function to modulate the expression of target genes, playing important roles in a wide range of physiological and pathological processes. The miRNAs in body fluids have received considerable attention as potential biomarkers of various diseases. In this study, we compared the changes of the plasma miRNA expressions by acute liver injury (hepatocellular injury or cholestasis) and chronic liver injury (steatosis, steatohepatitis and fibrosis) using rat models made by the administration of chemicals or special diets. Using miRNA array analysis, we found that the levels of a large number of miRNAs (121-317 miRNAs) were increased over 2-fold and the levels of a small number of miRNAs (6-35 miRNAs) were decreased below 0.5-fold in all models except in a model of cholestasis caused by bile duct ligation. Interestingly, the expression profiles were different between the models, and the hierarchical clustering analysis discriminated between the acute and chronic liver injuries. In addition, miRNAs whose expressions were typically changed in each type of liver injury could be specified. It is notable that, in acute liver injury models, the plasma level of miR-122, the most abundant miRNA in the liver, was more quickly and dramatically increased than the plasma aminotransferase level, reflecting the extent of hepatocellular injury. This study demonstrated that the plasma miRNA profiles could reflect the types of liver injury (e.g. acute/chronic liver injury or hepatocellular injury/cholestasis/steatosis/steatohepatitis/fibrosis) and identified the miRNAs that could be specific and sensitive biomarkers of liver injury.Yu YamauraMiki NakajimaShingo TakagiTatsuki FukamiKoichi TsuneyamaTsuyoshi YokoiPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 2, p e30250 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Yu Yamaura
Miki Nakajima
Shingo Takagi
Tatsuki Fukami
Koichi Tsuneyama
Tsuyoshi Yokoi
Plasma microRNA profiles in rat models of hepatocellular injury, cholestasis, and steatosis.
description MicroRNAs (miRNAs) are small RNA molecules that function to modulate the expression of target genes, playing important roles in a wide range of physiological and pathological processes. The miRNAs in body fluids have received considerable attention as potential biomarkers of various diseases. In this study, we compared the changes of the plasma miRNA expressions by acute liver injury (hepatocellular injury or cholestasis) and chronic liver injury (steatosis, steatohepatitis and fibrosis) using rat models made by the administration of chemicals or special diets. Using miRNA array analysis, we found that the levels of a large number of miRNAs (121-317 miRNAs) were increased over 2-fold and the levels of a small number of miRNAs (6-35 miRNAs) were decreased below 0.5-fold in all models except in a model of cholestasis caused by bile duct ligation. Interestingly, the expression profiles were different between the models, and the hierarchical clustering analysis discriminated between the acute and chronic liver injuries. In addition, miRNAs whose expressions were typically changed in each type of liver injury could be specified. It is notable that, in acute liver injury models, the plasma level of miR-122, the most abundant miRNA in the liver, was more quickly and dramatically increased than the plasma aminotransferase level, reflecting the extent of hepatocellular injury. This study demonstrated that the plasma miRNA profiles could reflect the types of liver injury (e.g. acute/chronic liver injury or hepatocellular injury/cholestasis/steatosis/steatohepatitis/fibrosis) and identified the miRNAs that could be specific and sensitive biomarkers of liver injury.
format article
author Yu Yamaura
Miki Nakajima
Shingo Takagi
Tatsuki Fukami
Koichi Tsuneyama
Tsuyoshi Yokoi
author_facet Yu Yamaura
Miki Nakajima
Shingo Takagi
Tatsuki Fukami
Koichi Tsuneyama
Tsuyoshi Yokoi
author_sort Yu Yamaura
title Plasma microRNA profiles in rat models of hepatocellular injury, cholestasis, and steatosis.
title_short Plasma microRNA profiles in rat models of hepatocellular injury, cholestasis, and steatosis.
title_full Plasma microRNA profiles in rat models of hepatocellular injury, cholestasis, and steatosis.
title_fullStr Plasma microRNA profiles in rat models of hepatocellular injury, cholestasis, and steatosis.
title_full_unstemmed Plasma microRNA profiles in rat models of hepatocellular injury, cholestasis, and steatosis.
title_sort plasma microrna profiles in rat models of hepatocellular injury, cholestasis, and steatosis.
publisher Public Library of Science (PLoS)
publishDate 2012
url https://doaj.org/article/0984a55d289d4135b90de3377be46fc1
work_keys_str_mv AT yuyamaura plasmamicrornaprofilesinratmodelsofhepatocellularinjurycholestasisandsteatosis
AT mikinakajima plasmamicrornaprofilesinratmodelsofhepatocellularinjurycholestasisandsteatosis
AT shingotakagi plasmamicrornaprofilesinratmodelsofhepatocellularinjurycholestasisandsteatosis
AT tatsukifukami plasmamicrornaprofilesinratmodelsofhepatocellularinjurycholestasisandsteatosis
AT koichitsuneyama plasmamicrornaprofilesinratmodelsofhepatocellularinjurycholestasisandsteatosis
AT tsuyoshiyokoi plasmamicrornaprofilesinratmodelsofhepatocellularinjurycholestasisandsteatosis
_version_ 1718423390008639488