The Interstitial Collagens of Fish

Author(s):  
Shigeru Kimura
1981 ◽  
Vol 89 (2) ◽  
pp. 276-283 ◽  
Author(s):  
P Ekblom ◽  
E Lehtonen ◽  
L Saxén ◽  
R Timpl

Conversion of the nephrogenic mesenchyme into epithelial tubules requires an inductive stimulus from the ureter bud. Here we show with immunofluorescence techniques that the undifferentiated mesenchyme before induction expresses uniformly type I and type III collagens. Induction both in vivo and in vitro leads to a loss of these proteins and to the appearance of basement membrane components including type IV collagen. This change correlates both spatially and temporally with the determination of the mesenchyme and precedes and morphological events. During morphogenesis, type IV collagen concentrates at the borders of the developing tubular structures where, by electron microscopy, a thin, often discontinuous basal lamina was seen to cover the first pretubular cell aggregates. Subsequently, the differentiating tubules were surrounded by a well-developed basal lamina. No loss of the interstitial collagens was seen in the metanephric mesenchyme when brought into contact with noninducing tissues or when cultured alone. Similar observations were made with nonnephrogenic mesenchyme (salivary, lung) when exposed to various heterotypic tissues known to induce tubules in the nephrogenic mesenchyme. The sequential shift in the composition of the extracellular matrix from an interstitial, mesenchymal type to a differentiated, epithelial type is so far the first detectable response of the nephrogenic mesenchyme to the tubule-inducing signal.


2001 ◽  
Vol 277 (5) ◽  
pp. 3242-3246 ◽  
Author(s):  
Rajan Somasundaram ◽  
Martin Ruehl ◽  
Benjamin Schaefer ◽  
Monika Schmid ◽  
Renate Ackermann ◽  
...  

2008 ◽  
Vol 77 (2) ◽  
pp. 867-876 ◽  
Author(s):  
Jürgen Baumert ◽  
Karl-Hermann Schmidt ◽  
Annett Eitner ◽  
Eberhard Straube ◽  
Jürgen Rödel

ABSTRACT Chlamydia pneumoniae infection has been associated with chronic obstructive airway disease (COPD), asthma, and atherosclerosis. Inflammation and airway remodeling in asthma and COPD result in subepithelial fibrosis that is characterized by the deposition of interstitial collagens and fibronectin. The progression of atherosclerosis is also accompanied by an increased production of interstitial collagens in the intima. As shown by reverse transcription-PCR and immunoblotting, infection of human fibroblasts and smooth muscle cells by C. pneumoniae TW-183 downregulated the expression of type I and III collagen and fibronectin, whereas the level of type IV collagen remained unchanged. Conditioned medium from infected fibroblasts as well as epithelial WISH cells also reduced the expression of interstitial collagens and fibronectin in uninfected cells. In experiments using blocking antibodies, beta interferon was found to contribute to the inhibitory effects of conditioned medium collected from infected fibroblasts. In contrast, downregulation of matrix protein expression by conditioned medium from epithelial cells was caused by interleukin-1α, which was not secreted from fibroblasts following chlamydial infection. C. pneumoniae-mediated inhibition of collagen and fibronectin expression was diminished following transfection of fibroblasts with specific small interfering RNA targeting the transcription factor CCAAT/enhancer-binding protein β. The downregulation of interstitial collagens and fibronectin by the Chlamydia-induced host cell cytokine response may modulate tissue remodeling processes in airway diseases. In atherosclerosis the inhibition of collagen synthesis by C. pneumoniae infection may promote plaque vulnerability, thereby increasing the risk of plaque rupture.


1991 ◽  
Vol 195 (1) ◽  
pp. 171-176 ◽  
Author(s):  
Dan T. Simionescu ◽  
Nicholas A. Kefalides

1991 ◽  
Vol 221 (1) ◽  
pp. 209-223 ◽  
Author(s):  
Francoise Gaill ◽  
Hanna Wiedemann ◽  
Karlheinz Mann ◽  
Klaus Kühn ◽  
Rupert Timpl ◽  
...  

Development ◽  
1988 ◽  
Vol 103 (2) ◽  
pp. 259-267 ◽  
Author(s):  
Y. Fukuda ◽  
Y. Masuda ◽  
J. Kishi ◽  
Y. Hashimoto ◽  
T. Hayakawa ◽  
...  

An interstitial collagenase was purified from the explant medium of bovine dental pulp and was shown to degrade collagens I and III but not IV and V. The enzyme halted cleft initiation in the epithelium of 12-day mouse embryonic submandibular glands in vitro, indicating the active involvement of interstitial collagens in the branching morphogenesis. Transmission electron microscopic observation of the intact 12-day gland without any clefts showed the scattered localization of a few collagen fibrils at the epithelial-mesenchymal interface of the bulb and also revealed the presence of numerous microfibrils around the stalk. Collagen bundles were regularly seen close to the wavy basal lamina at the bottom of clefts of the intact 13-day gland and 12-day gland cultured for 17 h under normal conditions. Mesenchymal cells were found in the clefts together with the frequent localization of peripheral nerve fibres and capillary endothelial cells. The collagen bundles were more often observed in the 12-day gland cultured in the presence of bovine dental pulp collagenase inhibitor, which had been shown to enhance cleft formation. In contrast, collagen fibrils were rarely found at the epithelial-mesenchymal interface of the 12-day gland cultured in the presence of Clostridial or bovine dental pulp collagenase. The findings indicated that the formation of interstitial collagen bundles is essential to form clefts in the epithelium both in vivo and in vitro.


1997 ◽  
Vol 272 (4) ◽  
pp. 2446-2451 ◽  
Author(s):  
Eiko Ohuchi ◽  
Kazushi Imai ◽  
Yutaka Fujii ◽  
Hiroshi Sato ◽  
Motoharu Seiki ◽  
...  

1991 ◽  
Vol 13 (3) ◽  
pp. 140-146 ◽  
Author(s):  
Veronica Glattauer ◽  
John A.M. Ramshaw ◽  
Tracy A. Tebb ◽  
Jerome A. Werkmeister

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