COLLAGEN BIOSYNTHESIS AND ISOMORPHISM IN A CASE OF EHLERS-DANLOS SYNDROME TYPE-VI

被引:11
作者
CHAMSON, A
BERBIS, P
FABRE, JF
PRIVAT, Y
FREY, J
机构
[1] HOTEL DIEU, CLIN DERMATOL MARSEILLE, 6 PL DAVIEL, F-13002 MARSEILLE, FRANCE
[2] FAC MED ST ETIENNE, BIOCHIM LAB, F-42023 ST ETIENNE 2, FRANCE
关键词
D O I
10.1007/BF00431222
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Collagen metabolism was studied in fibroblasts grown from a skin biopsy specimen of a patient who presented the striking clinical features of Ehlers-Danlos syndrome and, in particular, hyperextensibility of the skin, hypermobility of the joints, and kyphoscoliosis. A reduction in lysine hydroxylation, characteristic of Ehlers-Danlos Type VI, was observed after labeling of the collagen with 14C-proline and 3H-lysine. Other modifications in the collagen metabolism of fibroblast cultures were noted, including an increase in collagen and total protein synthesis, and an increase in both the Type I and Type III collagen. The percentage of Type III collagen was, however, lower than in the control fibroblasts. The results point out the complexity of collagen disturbances in Ehlers-Danlos Type VI.
引用
收藏
页码:303 / 307
页数:5
相关论文
共 14 条
[2]  
BYERS PH, 1981, LAB INVEST, V44, P336
[3]  
CHANDRAKASAN G, 1976, J BIOL CHEM, V251, P6062
[4]  
FREY J, 1967, B SOC CHIM BIOL, V49, P1221
[5]   EHLERS-DANLOS SYNDROME TYPE-VI - COLLAGEN TYPE SPECIFICITY OF DEFECTIVE LYSYL HYDROXYLATION IN VARIOUS TISSUES [J].
IHME, A ;
KRIEG, T ;
NERLICH, A ;
FELDMANN, U ;
RAUTERBERG, J ;
GLANVILLE, RW ;
EDEL, G ;
MULLER, PK .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1984, 83 (03) :161-165
[6]   LYSYL-PROTOCOLLAGEN HYDROXYLASE DEFICIENCY IN FIBROBLASTS FROM SIBLINGS GS WITH HYDROXYLYSINE-DEFICIENT COLLAGEN [J].
KRANE, SM ;
PINNELL, SR ;
ERBE, RW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1972, 69 (10) :2899-&
[7]   MOLECULAR DEFECTS OF COLLAGEN-METABOLISM IN THE EHLERS-DANLOS SYNDROME [J].
KRIEG, T ;
IHME, A ;
WEBER, L ;
KIRSCH, E ;
MUELLER, PK .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 1981, 20 (06) :415-425
[8]   BIOCHEMICAL CHARACTERISTICS OF EHLERS-DANLOS SYNDROME TYPE-VI IN A FAMILY WITH ONE AFFECTED INFANT [J].
KRIEG, T ;
FELDMANN, U ;
KESSLER, W ;
MULLER, PK .
HUMAN GENETICS, 1979, 46 (01) :41-49
[9]   CHROMATOGRAPHIC SEPARATION AND AMINO ACID COMPOSITION OF SUBUNITS OF SEVERAL COLLAGENS [J].
PIEZ, KA ;
LEWIS, MS ;
EIGNER, EA .
BIOCHEMISTRY, 1963, 2 (01) :58-+
[10]   HERITABLE DISORDER OF CONNECTIVE-TISSUE - HYDROXYLYSINE-DEFICIENT COLLAGEN DISEASE [J].
PINNELL, SR ;
KRANE, SM ;
GLIMCHER, MJ ;
KENZORA, JE .
NEW ENGLAND JOURNAL OF MEDICINE, 1972, 286 (19) :1013-&