Hepatic stellate cells and parasite-induced liver fibrosis
Abstract Fibrogenesis is a common feature of many diseases where there is severe insult to the liver. The hepatic stellate cell trans-differentiation into a myofibroblast has been identified as an important event in liver fibrogenesis and has been well investigated over the last few years in a numbe...
Ausführliche Beschreibung
Autor*in: |
Anthony, Barrie [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2010 |
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Schlagwörter: |
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Anmerkung: |
© Anthony et al; licensee BioMed Central Ltd. 2010 |
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Übergeordnetes Werk: |
Enthalten in: Parasites & vectors - London : BioMed Central, 2008, 3(2010), 1 vom: 21. Juli |
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Übergeordnetes Werk: |
volume:3 ; year:2010 ; number:1 ; day:21 ; month:07 |
Links: |
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DOI / URN: |
10.1186/1756-3305-3-60 |
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Katalog-ID: |
SPR030166691 |
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10.1186/1756-3305-3-60 doi (DE-627)SPR030166691 (SPR)1756-3305-3-60-e DE-627 ger DE-627 rakwb eng Anthony, Barrie verfasserin aut Hepatic stellate cells and parasite-induced liver fibrosis 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Anthony et al; licensee BioMed Central Ltd. 2010 Abstract Fibrogenesis is a common feature of many diseases where there is severe insult to the liver. The hepatic stellate cell trans-differentiation into a myofibroblast has been identified as an important event in liver fibrogenesis and has been well investigated over the last few years in a number of liver diseases. The trans-differentiation process can be monitored in vitro by evaluation of biomarkers that are characteristic of normal quiescent hepatic stellate cells or activated myofibroblasts. Two major parasitic diseases associated with liver injury and fibrosis are schistosomiasis and echinococcosis. Recent studies have highlighted a role for activated hepatic stellate cells in both murine and human schistosomiasis as well as demonstrating that schistosome antigens are able to regulate this trans-differentiation process. Study of the hepatic stellate cell and its interaction with parasite-derived antigens may be pivotal in our understanding of the pathology associated with schistosomiasis and other parasitic diseases, including echinococcosis, as well as revealing new information on the trans-differentiation process in this cell type. Schistosomiasis (dpeaa)DE-He213 Hepatic Stellate Cell (dpeaa)DE-He213 Echinococcosis (dpeaa)DE-He213 Hepatic Stellate Cell Activation (dpeaa)DE-He213 Alveolar Echinococcosis (dpeaa)DE-He213 Allen, Jeremy T aut Li, Yuesheng S aut McManus, Donald P aut Enthalten in Parasites & vectors London : BioMed Central, 2008 3(2010), 1 vom: 21. Juli (DE-627)558690076 (DE-600)2409480-8 1756-3305 nnns volume:3 year:2010 number:1 day:21 month:07 https://dx.doi.org/10.1186/1756-3305-3-60 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 3 2010 1 21 07 |
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10.1186/1756-3305-3-60 doi (DE-627)SPR030166691 (SPR)1756-3305-3-60-e DE-627 ger DE-627 rakwb eng Anthony, Barrie verfasserin aut Hepatic stellate cells and parasite-induced liver fibrosis 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Anthony et al; licensee BioMed Central Ltd. 2010 Abstract Fibrogenesis is a common feature of many diseases where there is severe insult to the liver. The hepatic stellate cell trans-differentiation into a myofibroblast has been identified as an important event in liver fibrogenesis and has been well investigated over the last few years in a number of liver diseases. The trans-differentiation process can be monitored in vitro by evaluation of biomarkers that are characteristic of normal quiescent hepatic stellate cells or activated myofibroblasts. Two major parasitic diseases associated with liver injury and fibrosis are schistosomiasis and echinococcosis. Recent studies have highlighted a role for activated hepatic stellate cells in both murine and human schistosomiasis as well as demonstrating that schistosome antigens are able to regulate this trans-differentiation process. Study of the hepatic stellate cell and its interaction with parasite-derived antigens may be pivotal in our understanding of the pathology associated with schistosomiasis and other parasitic diseases, including echinococcosis, as well as revealing new information on the trans-differentiation process in this cell type. Schistosomiasis (dpeaa)DE-He213 Hepatic Stellate Cell (dpeaa)DE-He213 Echinococcosis (dpeaa)DE-He213 Hepatic Stellate Cell Activation (dpeaa)DE-He213 Alveolar Echinococcosis (dpeaa)DE-He213 Allen, Jeremy T aut Li, Yuesheng S aut McManus, Donald P aut Enthalten in Parasites & vectors London : BioMed Central, 2008 3(2010), 1 vom: 21. Juli (DE-627)558690076 (DE-600)2409480-8 1756-3305 nnns volume:3 year:2010 number:1 day:21 month:07 https://dx.doi.org/10.1186/1756-3305-3-60 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 3 2010 1 21 07 |
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10.1186/1756-3305-3-60 doi (DE-627)SPR030166691 (SPR)1756-3305-3-60-e DE-627 ger DE-627 rakwb eng Anthony, Barrie verfasserin aut Hepatic stellate cells and parasite-induced liver fibrosis 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Anthony et al; licensee BioMed Central Ltd. 2010 Abstract Fibrogenesis is a common feature of many diseases where there is severe insult to the liver. The hepatic stellate cell trans-differentiation into a myofibroblast has been identified as an important event in liver fibrogenesis and has been well investigated over the last few years in a number of liver diseases. The trans-differentiation process can be monitored in vitro by evaluation of biomarkers that are characteristic of normal quiescent hepatic stellate cells or activated myofibroblasts. Two major parasitic diseases associated with liver injury and fibrosis are schistosomiasis and echinococcosis. Recent studies have highlighted a role for activated hepatic stellate cells in both murine and human schistosomiasis as well as demonstrating that schistosome antigens are able to regulate this trans-differentiation process. Study of the hepatic stellate cell and its interaction with parasite-derived antigens may be pivotal in our understanding of the pathology associated with schistosomiasis and other parasitic diseases, including echinococcosis, as well as revealing new information on the trans-differentiation process in this cell type. Schistosomiasis (dpeaa)DE-He213 Hepatic Stellate Cell (dpeaa)DE-He213 Echinococcosis (dpeaa)DE-He213 Hepatic Stellate Cell Activation (dpeaa)DE-He213 Alveolar Echinococcosis (dpeaa)DE-He213 Allen, Jeremy T aut Li, Yuesheng S aut McManus, Donald P aut Enthalten in Parasites & vectors London : BioMed Central, 2008 3(2010), 1 vom: 21. Juli (DE-627)558690076 (DE-600)2409480-8 1756-3305 nnns volume:3 year:2010 number:1 day:21 month:07 https://dx.doi.org/10.1186/1756-3305-3-60 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 3 2010 1 21 07 |
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10.1186/1756-3305-3-60 doi (DE-627)SPR030166691 (SPR)1756-3305-3-60-e DE-627 ger DE-627 rakwb eng Anthony, Barrie verfasserin aut Hepatic stellate cells and parasite-induced liver fibrosis 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Anthony et al; licensee BioMed Central Ltd. 2010 Abstract Fibrogenesis is a common feature of many diseases where there is severe insult to the liver. The hepatic stellate cell trans-differentiation into a myofibroblast has been identified as an important event in liver fibrogenesis and has been well investigated over the last few years in a number of liver diseases. The trans-differentiation process can be monitored in vitro by evaluation of biomarkers that are characteristic of normal quiescent hepatic stellate cells or activated myofibroblasts. Two major parasitic diseases associated with liver injury and fibrosis are schistosomiasis and echinococcosis. Recent studies have highlighted a role for activated hepatic stellate cells in both murine and human schistosomiasis as well as demonstrating that schistosome antigens are able to regulate this trans-differentiation process. Study of the hepatic stellate cell and its interaction with parasite-derived antigens may be pivotal in our understanding of the pathology associated with schistosomiasis and other parasitic diseases, including echinococcosis, as well as revealing new information on the trans-differentiation process in this cell type. Schistosomiasis (dpeaa)DE-He213 Hepatic Stellate Cell (dpeaa)DE-He213 Echinococcosis (dpeaa)DE-He213 Hepatic Stellate Cell Activation (dpeaa)DE-He213 Alveolar Echinococcosis (dpeaa)DE-He213 Allen, Jeremy T aut Li, Yuesheng S aut McManus, Donald P aut Enthalten in Parasites & vectors London : BioMed Central, 2008 3(2010), 1 vom: 21. Juli (DE-627)558690076 (DE-600)2409480-8 1756-3305 nnns volume:3 year:2010 number:1 day:21 month:07 https://dx.doi.org/10.1186/1756-3305-3-60 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 3 2010 1 21 07 |
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10.1186/1756-3305-3-60 doi (DE-627)SPR030166691 (SPR)1756-3305-3-60-e DE-627 ger DE-627 rakwb eng Anthony, Barrie verfasserin aut Hepatic stellate cells and parasite-induced liver fibrosis 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Anthony et al; licensee BioMed Central Ltd. 2010 Abstract Fibrogenesis is a common feature of many diseases where there is severe insult to the liver. The hepatic stellate cell trans-differentiation into a myofibroblast has been identified as an important event in liver fibrogenesis and has been well investigated over the last few years in a number of liver diseases. The trans-differentiation process can be monitored in vitro by evaluation of biomarkers that are characteristic of normal quiescent hepatic stellate cells or activated myofibroblasts. Two major parasitic diseases associated with liver injury and fibrosis are schistosomiasis and echinococcosis. Recent studies have highlighted a role for activated hepatic stellate cells in both murine and human schistosomiasis as well as demonstrating that schistosome antigens are able to regulate this trans-differentiation process. Study of the hepatic stellate cell and its interaction with parasite-derived antigens may be pivotal in our understanding of the pathology associated with schistosomiasis and other parasitic diseases, including echinococcosis, as well as revealing new information on the trans-differentiation process in this cell type. Schistosomiasis (dpeaa)DE-He213 Hepatic Stellate Cell (dpeaa)DE-He213 Echinococcosis (dpeaa)DE-He213 Hepatic Stellate Cell Activation (dpeaa)DE-He213 Alveolar Echinococcosis (dpeaa)DE-He213 Allen, Jeremy T aut Li, Yuesheng S aut McManus, Donald P aut Enthalten in Parasites & vectors London : BioMed Central, 2008 3(2010), 1 vom: 21. Juli (DE-627)558690076 (DE-600)2409480-8 1756-3305 nnns volume:3 year:2010 number:1 day:21 month:07 https://dx.doi.org/10.1186/1756-3305-3-60 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 3 2010 1 21 07 |
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Abstract Fibrogenesis is a common feature of many diseases where there is severe insult to the liver. The hepatic stellate cell trans-differentiation into a myofibroblast has been identified as an important event in liver fibrogenesis and has been well investigated over the last few years in a number of liver diseases. The trans-differentiation process can be monitored in vitro by evaluation of biomarkers that are characteristic of normal quiescent hepatic stellate cells or activated myofibroblasts. Two major parasitic diseases associated with liver injury and fibrosis are schistosomiasis and echinococcosis. Recent studies have highlighted a role for activated hepatic stellate cells in both murine and human schistosomiasis as well as demonstrating that schistosome antigens are able to regulate this trans-differentiation process. Study of the hepatic stellate cell and its interaction with parasite-derived antigens may be pivotal in our understanding of the pathology associated with schistosomiasis and other parasitic diseases, including echinococcosis, as well as revealing new information on the trans-differentiation process in this cell type. © Anthony et al; licensee BioMed Central Ltd. 2010 |
abstractGer |
Abstract Fibrogenesis is a common feature of many diseases where there is severe insult to the liver. The hepatic stellate cell trans-differentiation into a myofibroblast has been identified as an important event in liver fibrogenesis and has been well investigated over the last few years in a number of liver diseases. The trans-differentiation process can be monitored in vitro by evaluation of biomarkers that are characteristic of normal quiescent hepatic stellate cells or activated myofibroblasts. Two major parasitic diseases associated with liver injury and fibrosis are schistosomiasis and echinococcosis. Recent studies have highlighted a role for activated hepatic stellate cells in both murine and human schistosomiasis as well as demonstrating that schistosome antigens are able to regulate this trans-differentiation process. Study of the hepatic stellate cell and its interaction with parasite-derived antigens may be pivotal in our understanding of the pathology associated with schistosomiasis and other parasitic diseases, including echinococcosis, as well as revealing new information on the trans-differentiation process in this cell type. © Anthony et al; licensee BioMed Central Ltd. 2010 |
abstract_unstemmed |
Abstract Fibrogenesis is a common feature of many diseases where there is severe insult to the liver. The hepatic stellate cell trans-differentiation into a myofibroblast has been identified as an important event in liver fibrogenesis and has been well investigated over the last few years in a number of liver diseases. The trans-differentiation process can be monitored in vitro by evaluation of biomarkers that are characteristic of normal quiescent hepatic stellate cells or activated myofibroblasts. Two major parasitic diseases associated with liver injury and fibrosis are schistosomiasis and echinococcosis. Recent studies have highlighted a role for activated hepatic stellate cells in both murine and human schistosomiasis as well as demonstrating that schistosome antigens are able to regulate this trans-differentiation process. Study of the hepatic stellate cell and its interaction with parasite-derived antigens may be pivotal in our understanding of the pathology associated with schistosomiasis and other parasitic diseases, including echinococcosis, as well as revealing new information on the trans-differentiation process in this cell type. © Anthony et al; licensee BioMed Central Ltd. 2010 |
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score |
7.4002275 |