Homology of lubricin and superficial zone protein (SZP): products of megakaryocyte stimulating factor (MSF) gene expression by human synovial fibroblasts and articular chondrocytes localized to chromosome 1q25
Gd. Jay et al., Homology of lubricin and superficial zone protein (SZP): products of megakaryocyte stimulating factor (MSF) gene expression by human synovial fibroblasts and articular chondrocytes localized to chromosome 1q25, J ORTHOP R, 19(4), 2001, pp. 677-687
We have previously identified megakaryocyte stimulating factor (MSF) gene e
xpression by synovial fibroblasts as the origin of lubricin in the synovial
cavity. Lubricin is a mucinous glycoprotein responsible for the boundary l
ubrication of articular cartilage. MSF has a significant homology to vitron
ectin and is composed of 12 exons. RNA was purified from human synovial fib
roblasts and articular chondrocytes grown in vitro from tissue explants obt
ained from subjects without degenerative joint disease. RT-PCR was used wit
h multiple complimentary primer pairs spanning the central mucin expressing
exon 6 of the MSF gene and individual exons on both the N- and C-terminal
sides of exon 6. Exons 2, 4 and 5 appear to be variably expressed by synovi
al fibroblasts and articular chondrocytes. Lubricating mucin, in the form o
f MSF, is expressed by both chondrocytes and synovial fibroblasts in vitro.
Both lubricin and superficial zone protein (SZP), a related proteoglycan,
share a similar primary structure but could differ in posttranslational mod
ifications with O-linked oligosaccharides which are predominant in lubricin
and with limited amounts chondroitin and keratan sulfate found in SZP. Sin
ce most of the MSF exons are involved in the expression of lubricating muci
n, a strong homology to vitronectin persists. It is therefore appropriate t
o consider that both SZP and lubricin occupy a new class of biomolecules te
rmed tribonectins. Screening of a human genome bacterial artificial chromso
me (BAC) library with a cDNA primer pair complimentary for exon 6 identifie
d two clones. Both clones were complimentary for chromosome 1q25 by in situ
hybridization. This same locus was previously implicated in camptodactyl-a
rthropatliy-pericarditis syndrome (CAP) by genetic mapping. It is hypothesi
zed that CAP, a large joint arthropathy, may be associated with ineffective
boundary lubrication provided by synovial fluid. (C) 2001 Orthopaedic Rese
arch Society. Published by Elsevier Science Ltd. All rights reserved.