Gene expressions of small leucine-rich repeat proteoglycans and fibulin-5 are decreased in pelvic organ prolapse
Författare
Summary, in English
Few studies are performed on the sustainability of the pelvic floor extracellular matrix important for preventing development of pelvic organ prolapse (POP). Collagens I and III, the elastin-associated proteins fibrillin-1 and fibulin-5 and the small leucine-rich repeat proteoglycans (SLRPs) decorin, lumican and fibromodulin are involved in giving the tissue its mechanical properties. Para-urethral biopsies were obtained from 15 women, 6 pre- and 9 post-menopausal, with POP. Real-time reverse transcription-polymerase chain reaction and immunohistochemistry for collagen I, collagen III, fibrillin-1, fibulin-5, decorin, lumican and fibromodulin were performed and compared with 14 controls, 8 pre- and 6 post-menopausal. Statistical comparisons controlled for age changes in gene expressions. A 16-fold decrease in decorin mRNA expression, P = 0.0001, and 8-fold in lumican mRNA expression, P = 0.001, were discovered in premenopausal POP compared with matched controls. In all women with POP, there were lower gene expressions of fibromodulin, P = 0.004, and fibulin-5, P = 0.001, compared with all controls. All proteins were detectable by immunohistochemistry, showing a weaker staining for decorin in premenopausal POP. For the first time, we show substantially decreased gene signal for production of SLRPs, regulators of collagen fiber assembly and impairment in elastic fiber assembly by down-regulation of fibulin-5 in POP.
Avdelning/ar
- Åke Oldberg´s group
- Matrix Biology
Publiceringsår
2009
Språk
Engelska
Sidor
251-257
Publikation/Tidskrift/Serie
Molecular Human Reproduction
Volym
15
Issue
4
Dokumenttyp
Artikel i tidskrift
Förlag
Oxford University Press
Ämne
- Obstetrics, Gynecology and Reproductive Medicine
Nyckelord
- collagen
- elastin
- prolapse
- proteoglycan
- extracellular matrix
Status
Published
Forskningsgrupp
- Åke Oldberg´s group
- Matrix Biology
ISBN/ISSN/Övrigt
- ISSN: 1460-2407