Light microscopic and ultrastructural distribution of type VI collagen in human liver: alterations in chronic biliary disease

GRIFFITHS, M.R. ; SHEPHERD, M. ; FERRIER, R. ; SCHUPPAN, D. ; JAMES, O.F.W. ; BURT, A.D.

Oxford, UK : Blackwell Publishing Ltd
Published 1992
ISSN:
1365-2559
Source:
Blackwell Publishing Journal Backfiles 1879-2005
Topics:
Medicine
Notes:
We have investigated the distribution of type VI collagen in normal human liver obtained from cadaveric renal transplant donors, using a peroxidase-antiperoxidase method for light microscopic visualization, and an immunogold labelling method for ultrastructural localization. The distribution was compared with that of the more abundant interstitial collagen type III, using antibodies to amino terminal procollagen type III.Staining for type VI collagen was identified in Glisson's capsule, in portal tract stroma and within the space of Disse. Perisinusoidal staining showed intra-acinar heterogeneity with the intensity in acinar zones 2 and 3 being greater than in zone 1. Type III collagen was also found in the space of Disse although no significant intra-acinar variation in staining intensity was noted. Immuno-gold labelling for type VI collagen was demonstrated on amorphous or microfilamentous material lying between, and occasionally appearing to interconnect, cross-striated collagen fibrils, whereas labelling for amino terminal procollagen type III was exclusively on fibrils. Intracellular staining for type VI collagen was noted in perisinusoidal (Ito) cells. These results confirm that type VI collagen is a ubiquitous constituent of the normal hepatic extracellular matrix and suggest that it may be synthesized by perisinusoidal (Ito) cells.The distribution of type VI collagen was also studied in biopsy material from patients with different histological stages of primary biliary cirrhosis. Intense staining was noted around proliferating bile ductules within developing fibrous septa and in established septa of cirrhotic liver. These observations indicate that this ‘minor’ matrix component may play an important role in hepatic fibrogenesis.
Type of Medium:
Electronic Resource
URL:
_version_ 1798290212538810368
autor GRIFFITHS, M.R.
SHEPHERD, M.
FERRIER, R.
SCHUPPAN, D.
JAMES, O.F.W.
BURT, A.D.
autorsonst SCHUPPAN, D.
JAMES, O.F.W.
BURT, A.D.
book_url http://dx.doi.org/10.1111/j.1365-2559.1992.tb00404.x
datenlieferant nat_lic_papers
hauptsatz hsatz_simple
identnr NLZ239520211
insertion_date 2012-04-26
issn 1365-2559
journal_name Histopathology
materialart 1
notes We have investigated the distribution of type VI collagen in normal human liver obtained from cadaveric renal transplant donors, using a peroxidase-antiperoxidase method for light microscopic visualization, and an immunogold labelling method for ultrastructural localization. The distribution was compared with that of the more abundant interstitial collagen type III, using antibodies to amino terminal procollagen type III.Staining for type VI collagen was identified in Glisson's capsule, in portal tract stroma and within the space of Disse. Perisinusoidal staining showed intra-acinar heterogeneity with the intensity in acinar zones 2 and 3 being greater than in zone 1. Type III collagen was also found in the space of Disse although no significant intra-acinar variation in staining intensity was noted. Immuno-gold labelling for type VI collagen was demonstrated on amorphous or microfilamentous material lying between, and occasionally appearing to interconnect, cross-striated collagen fibrils, whereas labelling for amino terminal procollagen type III was exclusively on fibrils. Intracellular staining for type VI collagen was noted in perisinusoidal (Ito) cells. These results confirm that type VI collagen is a ubiquitous constituent of the normal hepatic extracellular matrix and suggest that it may be synthesized by perisinusoidal (Ito) cells.The distribution of type VI collagen was also studied in biopsy material from patients with different histological stages of primary biliary cirrhosis. Intense staining was noted around proliferating bile ductules within developing fibrous septa and in established septa of cirrhotic liver. These observations indicate that this ‘minor’ matrix component may play an important role in hepatic fibrogenesis.
package_name Blackwell Publishing
publikationsjahr_anzeige 1992
publikationsjahr_facette 1992
publikationsjahr_intervall 8009:1990-1994
publikationsjahr_sort 1992
publikationsort Oxford, UK
publisher Blackwell Publishing Ltd
reference 21 (1992), S. 0
search_space articles
shingle_author_1 GRIFFITHS, M.R.
SHEPHERD, M.
FERRIER, R.
SCHUPPAN, D.
JAMES, O.F.W.
BURT, A.D.
shingle_author_2 GRIFFITHS, M.R.
SHEPHERD, M.
FERRIER, R.
SCHUPPAN, D.
JAMES, O.F.W.
BURT, A.D.
shingle_author_3 GRIFFITHS, M.R.
SHEPHERD, M.
FERRIER, R.
SCHUPPAN, D.
JAMES, O.F.W.
BURT, A.D.
shingle_author_4 GRIFFITHS, M.R.
SHEPHERD, M.
FERRIER, R.
SCHUPPAN, D.
JAMES, O.F.W.
BURT, A.D.
shingle_catch_all_1 GRIFFITHS, M.R.
SHEPHERD, M.
FERRIER, R.
SCHUPPAN, D.
JAMES, O.F.W.
BURT, A.D.
Light microscopic and ultrastructural distribution of type VI collagen in human liver: alterations in chronic biliary disease
Blackwell Publishing Ltd
We have investigated the distribution of type VI collagen in normal human liver obtained from cadaveric renal transplant donors, using a peroxidase-antiperoxidase method for light microscopic visualization, and an immunogold labelling method for ultrastructural localization. The distribution was compared with that of the more abundant interstitial collagen type III, using antibodies to amino terminal procollagen type III.Staining for type VI collagen was identified in Glisson's capsule, in portal tract stroma and within the space of Disse. Perisinusoidal staining showed intra-acinar heterogeneity with the intensity in acinar zones 2 and 3 being greater than in zone 1. Type III collagen was also found in the space of Disse although no significant intra-acinar variation in staining intensity was noted. Immuno-gold labelling for type VI collagen was demonstrated on amorphous or microfilamentous material lying between, and occasionally appearing to interconnect, cross-striated collagen fibrils, whereas labelling for amino terminal procollagen type III was exclusively on fibrils. Intracellular staining for type VI collagen was noted in perisinusoidal (Ito) cells. These results confirm that type VI collagen is a ubiquitous constituent of the normal hepatic extracellular matrix and suggest that it may be synthesized by perisinusoidal (Ito) cells.The distribution of type VI collagen was also studied in biopsy material from patients with different histological stages of primary biliary cirrhosis. Intense staining was noted around proliferating bile ductules within developing fibrous septa and in established septa of cirrhotic liver. These observations indicate that this ‘minor’ matrix component may play an important role in hepatic fibrogenesis.
1365-2559
13652559
shingle_catch_all_2 GRIFFITHS, M.R.
SHEPHERD, M.
FERRIER, R.
SCHUPPAN, D.
JAMES, O.F.W.
BURT, A.D.
Light microscopic and ultrastructural distribution of type VI collagen in human liver: alterations in chronic biliary disease
Blackwell Publishing Ltd
We have investigated the distribution of type VI collagen in normal human liver obtained from cadaveric renal transplant donors, using a peroxidase-antiperoxidase method for light microscopic visualization, and an immunogold labelling method for ultrastructural localization. The distribution was compared with that of the more abundant interstitial collagen type III, using antibodies to amino terminal procollagen type III.Staining for type VI collagen was identified in Glisson's capsule, in portal tract stroma and within the space of Disse. Perisinusoidal staining showed intra-acinar heterogeneity with the intensity in acinar zones 2 and 3 being greater than in zone 1. Type III collagen was also found in the space of Disse although no significant intra-acinar variation in staining intensity was noted. Immuno-gold labelling for type VI collagen was demonstrated on amorphous or microfilamentous material lying between, and occasionally appearing to interconnect, cross-striated collagen fibrils, whereas labelling for amino terminal procollagen type III was exclusively on fibrils. Intracellular staining for type VI collagen was noted in perisinusoidal (Ito) cells. These results confirm that type VI collagen is a ubiquitous constituent of the normal hepatic extracellular matrix and suggest that it may be synthesized by perisinusoidal (Ito) cells.The distribution of type VI collagen was also studied in biopsy material from patients with different histological stages of primary biliary cirrhosis. Intense staining was noted around proliferating bile ductules within developing fibrous septa and in established septa of cirrhotic liver. These observations indicate that this ‘minor’ matrix component may play an important role in hepatic fibrogenesis.
1365-2559
13652559
shingle_catch_all_3 GRIFFITHS, M.R.
SHEPHERD, M.
FERRIER, R.
SCHUPPAN, D.
JAMES, O.F.W.
BURT, A.D.
Light microscopic and ultrastructural distribution of type VI collagen in human liver: alterations in chronic biliary disease
Blackwell Publishing Ltd
We have investigated the distribution of type VI collagen in normal human liver obtained from cadaveric renal transplant donors, using a peroxidase-antiperoxidase method for light microscopic visualization, and an immunogold labelling method for ultrastructural localization. The distribution was compared with that of the more abundant interstitial collagen type III, using antibodies to amino terminal procollagen type III.Staining for type VI collagen was identified in Glisson's capsule, in portal tract stroma and within the space of Disse. Perisinusoidal staining showed intra-acinar heterogeneity with the intensity in acinar zones 2 and 3 being greater than in zone 1. Type III collagen was also found in the space of Disse although no significant intra-acinar variation in staining intensity was noted. Immuno-gold labelling for type VI collagen was demonstrated on amorphous or microfilamentous material lying between, and occasionally appearing to interconnect, cross-striated collagen fibrils, whereas labelling for amino terminal procollagen type III was exclusively on fibrils. Intracellular staining for type VI collagen was noted in perisinusoidal (Ito) cells. These results confirm that type VI collagen is a ubiquitous constituent of the normal hepatic extracellular matrix and suggest that it may be synthesized by perisinusoidal (Ito) cells.The distribution of type VI collagen was also studied in biopsy material from patients with different histological stages of primary biliary cirrhosis. Intense staining was noted around proliferating bile ductules within developing fibrous septa and in established septa of cirrhotic liver. These observations indicate that this ‘minor’ matrix component may play an important role in hepatic fibrogenesis.
1365-2559
13652559
shingle_catch_all_4 GRIFFITHS, M.R.
SHEPHERD, M.
FERRIER, R.
SCHUPPAN, D.
JAMES, O.F.W.
BURT, A.D.
Light microscopic and ultrastructural distribution of type VI collagen in human liver: alterations in chronic biliary disease
Blackwell Publishing Ltd
We have investigated the distribution of type VI collagen in normal human liver obtained from cadaveric renal transplant donors, using a peroxidase-antiperoxidase method for light microscopic visualization, and an immunogold labelling method for ultrastructural localization. The distribution was compared with that of the more abundant interstitial collagen type III, using antibodies to amino terminal procollagen type III.Staining for type VI collagen was identified in Glisson's capsule, in portal tract stroma and within the space of Disse. Perisinusoidal staining showed intra-acinar heterogeneity with the intensity in acinar zones 2 and 3 being greater than in zone 1. Type III collagen was also found in the space of Disse although no significant intra-acinar variation in staining intensity was noted. Immuno-gold labelling for type VI collagen was demonstrated on amorphous or microfilamentous material lying between, and occasionally appearing to interconnect, cross-striated collagen fibrils, whereas labelling for amino terminal procollagen type III was exclusively on fibrils. Intracellular staining for type VI collagen was noted in perisinusoidal (Ito) cells. These results confirm that type VI collagen is a ubiquitous constituent of the normal hepatic extracellular matrix and suggest that it may be synthesized by perisinusoidal (Ito) cells.The distribution of type VI collagen was also studied in biopsy material from patients with different histological stages of primary biliary cirrhosis. Intense staining was noted around proliferating bile ductules within developing fibrous septa and in established septa of cirrhotic liver. These observations indicate that this ‘minor’ matrix component may play an important role in hepatic fibrogenesis.
1365-2559
13652559
shingle_title_1 Light microscopic and ultrastructural distribution of type VI collagen in human liver: alterations in chronic biliary disease
shingle_title_2 Light microscopic and ultrastructural distribution of type VI collagen in human liver: alterations in chronic biliary disease
shingle_title_3 Light microscopic and ultrastructural distribution of type VI collagen in human liver: alterations in chronic biliary disease
shingle_title_4 Light microscopic and ultrastructural distribution of type VI collagen in human liver: alterations in chronic biliary disease
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source_archive Blackwell Publishing Journal Backfiles 1879-2005
timestamp 2024-05-06T08:13:07.001Z
titel Light microscopic and ultrastructural distribution of type VI collagen in human liver: alterations in chronic biliary disease
titel_suche Light microscopic and ultrastructural distribution of type VI collagen in human liver: alterations in chronic biliary disease
topic WW-YZ
uid nat_lic_papers_NLZ239520211