scholarly journals Soluble EMMPRIN levels discriminate aortic ectasia in Marfan syndrome patients

Theranostics ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 2224-2234 ◽  
Author(s):  
Erica Rurali ◽  
Gianluca L. Perrucci ◽  
Raffaella Gaetano ◽  
Alessandro Pini ◽  
Donato Moschetta ◽  
...  
1985 ◽  
Vol 232 (1) ◽  
pp. 169-175 ◽  
Author(s):  
T Halme ◽  
M Jutila ◽  
T Vihersaari ◽  
P Oksman ◽  
N D Light ◽  
...  

Human aortic elastin reduced with [3H]borohydride was analysed by ion-exchange chromatography after alkali or acid hydrolysis. Alkali hydrolysates of elastins contained a radioactive peak that was eluted between proline and leucine. This peak was not present in foetal elastin, but its proportion increased steadily during aging. Aortic samples from patients with annulo-aortic ectasia (aneurysm of the ascending aorta), including one with classical Marfan syndrome, contained less elastin (CNBr-insoluble material) than did the age-matched controls. The proportion of radioactivity in the new peak of all these aortas was low when compared with age-matched controls. Gas-chromatographic/mass-spectrometric analysis suggested that it contained a cyclic derivative of a hydrated aldol-condensation product. The concentration of the cross-link precursors, lysine aldehyde and aldol-condensation product (estimated from the acid-hydrolysis product 6-chloronorleucine and the acid-degradation product of reduced aldol-condensation product) was high in very young aortas but remained quite stable after childhood. No differences were observed in cross-link profiles of acid hydrolysates between pathological and control aortas. A low proportion of radioactivity in the new peak may indicate the presence of young or immature elastin in the pathological aortas.


Author(s):  
M. V. Inberg ◽  
J. Niinikoski ◽  
V. Rantakokko ◽  
T. Savunen ◽  
E. Vänttinen

2018 ◽  
Vol 39 (suppl_1) ◽  
Author(s):  
E Rurali ◽  
G L Perrucci ◽  
R Gaetano ◽  
A Pini ◽  
D Moschetta ◽  
...  

1995 ◽  
Vol 3 ◽  
pp. 144-144
Author(s):  
K KOJA ◽  
Y KUSABA ◽  
Y KUNIYOSHI ◽  
K IHA ◽  
M AKASAKI ◽  
...  

Author(s):  
Douglas R. Keene ◽  
Magaret Fairhurst ◽  
Catherine C. Ridgway ◽  
Lynn Y. Sakai

Matrix microfibrils are present in the connective tissue matrices of all tissues. Following standard TEM processing, they appear in cross section as cylindrical fibrils 8-10 nm in diameter, often associated with amorphous elastin. They are also seen in the absence of amorphous elastin, for example in the shallow papillary layer of skin, and also in cartilage matrix (Figure 1). Negative stain and rotary shadowing studies suggest that microfibrils are composed of laterally associated globular structures connected by fine filamentous strands (“ beaded strings”), and that they are extendable. Immunoelectron microscopy has demonstrated that fibrillin, a 350 Kd glycoprotein, is distributed along all microfibrils with a relaxed periodicity of about 54 nm The gene coding for fibrillin has recently been identified and is defective in the Marfan syndrome.


2011 ◽  
Vol 44 (8) ◽  
pp. 54-55
Author(s):  
HOWARD P. LEVY
Keyword(s):  

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