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Morphological characterisation of portal myofibroblasts and hepatic stellate cells in the normal dog liver

BACKGROUND: Hepatic fibrosis is a common outcome of hepatic injury in both man and dog. Activated fibroblasts which develop myofibroblastic characteristics play an essential role in hepatic fibrogenesis, and are comprised of three subpopulations: 1) portal or septal myofibroblasts, 2) interface myof...

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Autores principales: IJzer, Jooske, Roskams, Tania, Molenbeek, Ronald F, Ultee, Ton, Penning, Louis C, Rothuizen, Jan, van den Ingh, Ted SGAM
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1660578/
https://www.ncbi.nlm.nih.gov/pubmed/17109742
http://dx.doi.org/10.1186/1476-5926-5-7
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author IJzer, Jooske
Roskams, Tania
Molenbeek, Ronald F
Ultee, Ton
Penning, Louis C
Rothuizen, Jan
van den Ingh, Ted SGAM
author_facet IJzer, Jooske
Roskams, Tania
Molenbeek, Ronald F
Ultee, Ton
Penning, Louis C
Rothuizen, Jan
van den Ingh, Ted SGAM
author_sort IJzer, Jooske
collection PubMed
description BACKGROUND: Hepatic fibrosis is a common outcome of hepatic injury in both man and dog. Activated fibroblasts which develop myofibroblastic characteristics play an essential role in hepatic fibrogenesis, and are comprised of three subpopulations: 1) portal or septal myofibroblasts, 2) interface myofibroblasts and 3) the perisinusoidally located hepatic stellate cells (HSC). The present study was performed to investigate the immunohistochemical characteristics of canine portal myofibroblasts (MF) and HSC in the normal unaffected liver as a basis for further studies on fibrogenesis in canine liver disease. RESULTS: In the formalin-fixed and paraffin embedded normal canine liver vimentin showed staining of hepatic fibroblasts, probably including MF in portal areas and around hepatic veins; however, HSC were in general negative. Desmin proved to react with both portal MF and HSC. A unique feature of these HSC was the positive immunostaining for alpha-smooth muscle actin (α-SMA) and muscle-specific actin clone HHF35 (HHF35), also portal MF stained positive with these antibodies. Synaptophysin and glial fibrillary acidic protein (GFAP) were consistently negative in the normal canine liver. In a frozen chronic hepatitis case (with expected activated hepatic MF and HSC), HSC were negative to synaptophysin, GFAP and NCAM. Transmission electron microscopy (TEM) immunogold labelling for α-SMA and HHF35 recognized the positive cells as HSC situated in the space of Disse. CONCLUSION: In the normal formalin-fixed and paraffin embedded canine liver hepatic portal MF and HSC can be identified by α-SMA, HHF35 and to a lesser extent desmin immunostaining. These antibodies can thus be used in further studies on hepatic fibrosis. Synaptophysin, GFAP and NCAM do not seem suitable for marking of canine HSC. The positivity of HSC for α-SMA and HHF35 in the normal canine liver may eventually reflect a more active regulation of hepatic sinusoidal flow by these HSC compared to other species.
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spelling pubmed-16605782006-11-24 Morphological characterisation of portal myofibroblasts and hepatic stellate cells in the normal dog liver IJzer, Jooske Roskams, Tania Molenbeek, Ronald F Ultee, Ton Penning, Louis C Rothuizen, Jan van den Ingh, Ted SGAM Comp Hepatol Research BACKGROUND: Hepatic fibrosis is a common outcome of hepatic injury in both man and dog. Activated fibroblasts which develop myofibroblastic characteristics play an essential role in hepatic fibrogenesis, and are comprised of three subpopulations: 1) portal or septal myofibroblasts, 2) interface myofibroblasts and 3) the perisinusoidally located hepatic stellate cells (HSC). The present study was performed to investigate the immunohistochemical characteristics of canine portal myofibroblasts (MF) and HSC in the normal unaffected liver as a basis for further studies on fibrogenesis in canine liver disease. RESULTS: In the formalin-fixed and paraffin embedded normal canine liver vimentin showed staining of hepatic fibroblasts, probably including MF in portal areas and around hepatic veins; however, HSC were in general negative. Desmin proved to react with both portal MF and HSC. A unique feature of these HSC was the positive immunostaining for alpha-smooth muscle actin (α-SMA) and muscle-specific actin clone HHF35 (HHF35), also portal MF stained positive with these antibodies. Synaptophysin and glial fibrillary acidic protein (GFAP) were consistently negative in the normal canine liver. In a frozen chronic hepatitis case (with expected activated hepatic MF and HSC), HSC were negative to synaptophysin, GFAP and NCAM. Transmission electron microscopy (TEM) immunogold labelling for α-SMA and HHF35 recognized the positive cells as HSC situated in the space of Disse. CONCLUSION: In the normal formalin-fixed and paraffin embedded canine liver hepatic portal MF and HSC can be identified by α-SMA, HHF35 and to a lesser extent desmin immunostaining. These antibodies can thus be used in further studies on hepatic fibrosis. Synaptophysin, GFAP and NCAM do not seem suitable for marking of canine HSC. The positivity of HSC for α-SMA and HHF35 in the normal canine liver may eventually reflect a more active regulation of hepatic sinusoidal flow by these HSC compared to other species. BioMed Central 2006-11-16 /pmc/articles/PMC1660578/ /pubmed/17109742 http://dx.doi.org/10.1186/1476-5926-5-7 Text en Copyright © 2006 IJzer et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
IJzer, Jooske
Roskams, Tania
Molenbeek, Ronald F
Ultee, Ton
Penning, Louis C
Rothuizen, Jan
van den Ingh, Ted SGAM
Morphological characterisation of portal myofibroblasts and hepatic stellate cells in the normal dog liver
title Morphological characterisation of portal myofibroblasts and hepatic stellate cells in the normal dog liver
title_full Morphological characterisation of portal myofibroblasts and hepatic stellate cells in the normal dog liver
title_fullStr Morphological characterisation of portal myofibroblasts and hepatic stellate cells in the normal dog liver
title_full_unstemmed Morphological characterisation of portal myofibroblasts and hepatic stellate cells in the normal dog liver
title_short Morphological characterisation of portal myofibroblasts and hepatic stellate cells in the normal dog liver
title_sort morphological characterisation of portal myofibroblasts and hepatic stellate cells in the normal dog liver
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1660578/
https://www.ncbi.nlm.nih.gov/pubmed/17109742
http://dx.doi.org/10.1186/1476-5926-5-7
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