Inhibition of glycosaminoglycan incorporation influences collagen network formation during cartilage matrix production

被引:8
作者
Bastiaansen-Jenniskens, Yvonne M. [1 ,2 ]
Koevoet, Wendy [3 ]
Jansen, Kaspar M. B. [4 ]
Verhaar, Jan A. N. [1 ]
DeGroot, Jeroen [2 ]
VanOsch, Gerjo J. V. M. [1 ,3 ]
机构
[1] Erasmus MC, Dept Orthopaed, Univ Med Ctr Rotterdam, NL-3000 CA Rotterdam, Netherlands
[2] TNO Qual Life, Business Unit BioSci, Leiden, Netherlands
[3] Erasmus MC, Dept Otorhinolaryngol, Univ Med Ctr Rotterdam, NL-3000 CA Rotterdam, Netherlands
[4] Delft Univ Technol, Fac 3mE, Dept Precis & Microsyst Engn, NL-2600 AA Delft, Netherlands
关键词
Glycosaminoglycan; Collagen; Cartilage matrix; Chondrocyte; BETA-D-XYLOSIDE; OSTEOARTHRITIC ARTICULAR-CARTILAGE; PROTEIN LINKAGE REGION; EMBRYONIC CHICK BRAIN; PROTEOGLYCAN SYNTHESIS; CHONDROITIN SULFATE; CELL-CULTURES; II COLLAGEN; BIOSYNTHESIS; CHONDROCYTES;
D O I
10.1016/j.bbrc.2008.12.028
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
TO understand cartilage degenerative diseases and improve repair procedures, we investigate the influence of glycosaminoglycans (GAGs) on cartilage matrix biochemistry and functionality. Bovine articular chondrocytes were cultured in alginate beads with(out) para-nitrophenyl-beta-D-xyloside (PNPX) to inhibit GAG incorporation into newly formed proteoglycans. As expected, GAG deposition in alginate beads decreased with increasing PNPX concentration. Next to GAGs, collagen deposition and cross-linking also decreased. In the presence of PNPX, GAGs and collagen were deposited further away from the chondrocyte than in the control and increased amounts were found in the Culture medium. These changes resulted in decreased functional properties of the construct. We conclude that in Our culture system, intact proteoglycans play a role in deposition of collagen and thus the formation of a functional matrix. The effect of less proteoglycans on the collagen network could explain why cartilage repair is ineffective in osteoarthritis and help us with development of new therapies. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:222 / 226
页数:5
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