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Discovery of cytoglobin and its roles in physiology and pathology of hepatic stellate cells

Cytoglobin (CYGB), a new member of the globin family, was discovered in 2001 as a protein associated with stellate cell activation (stellate cell activation-associated protein [STAP]). Knowledge of CYGB, including its crystal, gene, and protein structures as well as its physiological and pathologica...

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Autores principales: YOSHIZATO, Katsutoshi, THUY, Le Thi Thanh, SHIOTA, Goshi, KAWADA, Norifumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Academy 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4925767/
https://www.ncbi.nlm.nih.gov/pubmed/26972599
http://dx.doi.org/10.2183/pjab.92.77
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author YOSHIZATO, Katsutoshi
THUY, Le Thi Thanh
SHIOTA, Goshi
KAWADA, Norifumi
author_facet YOSHIZATO, Katsutoshi
THUY, Le Thi Thanh
SHIOTA, Goshi
KAWADA, Norifumi
author_sort YOSHIZATO, Katsutoshi
collection PubMed
description Cytoglobin (CYGB), a new member of the globin family, was discovered in 2001 as a protein associated with stellate cell activation (stellate cell activation-associated protein [STAP]). Knowledge of CYGB, including its crystal, gene, and protein structures as well as its physiological and pathological importance, has increased progressively. We investigated the roles of oxygen (O(2))-binding CYGB as STAP in hepatic stellate cells (HSCs) to understand the part played by this protein in their pathophysiological activities. Studies involving CYGB-gene-deleted mice have led us to suppose that CYGB functions as a regulator of O(2) homeostasis; when O(2) homeostasis is disrupted, HSCs are activated and play a key role(s) in hepatic fibrogenesis. In this review, we discuss the rationale for this hypothesis.
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spelling pubmed-49257672016-07-07 Discovery of cytoglobin and its roles in physiology and pathology of hepatic stellate cells YOSHIZATO, Katsutoshi THUY, Le Thi Thanh SHIOTA, Goshi KAWADA, Norifumi Proc Jpn Acad Ser B Phys Biol Sci Review Cytoglobin (CYGB), a new member of the globin family, was discovered in 2001 as a protein associated with stellate cell activation (stellate cell activation-associated protein [STAP]). Knowledge of CYGB, including its crystal, gene, and protein structures as well as its physiological and pathological importance, has increased progressively. We investigated the roles of oxygen (O(2))-binding CYGB as STAP in hepatic stellate cells (HSCs) to understand the part played by this protein in their pathophysiological activities. Studies involving CYGB-gene-deleted mice have led us to suppose that CYGB functions as a regulator of O(2) homeostasis; when O(2) homeostasis is disrupted, HSCs are activated and play a key role(s) in hepatic fibrogenesis. In this review, we discuss the rationale for this hypothesis. The Japan Academy 2016-03-11 /pmc/articles/PMC4925767/ /pubmed/26972599 http://dx.doi.org/10.2183/pjab.92.77 Text en © 2016 The Japan Academy This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
YOSHIZATO, Katsutoshi
THUY, Le Thi Thanh
SHIOTA, Goshi
KAWADA, Norifumi
Discovery of cytoglobin and its roles in physiology and pathology of hepatic stellate cells
title Discovery of cytoglobin and its roles in physiology and pathology of hepatic stellate cells
title_full Discovery of cytoglobin and its roles in physiology and pathology of hepatic stellate cells
title_fullStr Discovery of cytoglobin and its roles in physiology and pathology of hepatic stellate cells
title_full_unstemmed Discovery of cytoglobin and its roles in physiology and pathology of hepatic stellate cells
title_short Discovery of cytoglobin and its roles in physiology and pathology of hepatic stellate cells
title_sort discovery of cytoglobin and its roles in physiology and pathology of hepatic stellate cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4925767/
https://www.ncbi.nlm.nih.gov/pubmed/26972599
http://dx.doi.org/10.2183/pjab.92.77
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