J Korean Soc Spine Surg. 2005 Mar;12(1):12-21. Korean.
Published online Mar 31, 2005.
Copyright © 2005 Korean Society of Spine Surgery
Original Article

Role of Matrix Metalloproteinase-3 in Degenerative Lumbar Scoliosis

Seong-Tae Cho, M.D., Jong-Min Sohn, M.D., Nan-Kyung Ha, M.D., Kee-Yong Ha, M.D.,# Kwang-Young Choi, M.D. and Young-Wan Suh, M.D.
    • Department of Orthopedic Surgery, Our Lady of Mercy Hospital, The Catholic University of Korea, College of Medicine, Inchon, Korea.
    • #Department of Orthopedic Surgery, Kang-Nam St. Mary's Hospital, The Catholic University of Korea, College of Medicine, Seoul, Korea.

Abstract

Purpose

This study was performed to investigate the differences in the expression of matrix metalloproteinase-3 in degenerative scoliosis compared with other degenerative disc disease of the spine.

Materials and Methods

The intervertebral disc materials were obtained during discectomies. Six, 13 and 12 cases of herniated nucleus pulposus, spinal stenosis and degenerative lumbar scoliosis, respectively, were included in the experimental group. The expression of MMP-3 was evaluated three times that of the means, in the immunohistochemical staining, western blotting using anti human MMP-3 antibody and RT-PCR with MMP-3 primer, respectively.

Results

On the immunohistochemical stains, extensive and strong staining was noted in the discs of degenerative lumbar scoliosis compared to those with spinal stenosis and HNP. In the western blotting, greater expression of MMP-3 was noted in the discs of degenerative lumbar scoliosis (mean optical density: 20.68) than in other degenerative disc diseases (SS: 6.24, HNP: 2.0). In the RT-PCR, a similar result was shown (DLS: 62.1, SS: 27.4 & HNP: 10.4). There were statistically significant differences between degenerative lumbar scoliosis and degenerative disc disease (p<0.05).

Conclusion

Rapid degeneration of the intervertebral disc might be an important factor in the pathogenesis of degenerative lumbar scoliosis. MMP-3 could be a key enzyme for the rapid degeneration of the intervertebral discs, especially in degenerative lumbar scoliosis.

Keywords
Intervertebral disc; Degenerative lumbar scoliosis; MMP-3

Figures

Fig. 1
(A,B) Photomicrographs of immunohistochemical staining for MMP-3(counter-stain with H-E, ×100, ×400). Slight expression of MMP-3 in HNP.

Fig. 2
(A,B) Photomicrographs of immunohistochemical staining for MMP-3(counter-stain with H-E, ×100, ×400). Degenerations of the disc and expression of MMP-3 are noted in the sample, obtained in SS. Profuse expression of MMP-3 with reddish area and more cellular proliferation than HNP are noted.

Fig. 3
(A,B) Immunohistochemical staining for MMP-3(counter-stain with H-E, ×100, ×400). Severe disc degeneration with many cleft of the disc material and cellular proliferation are noted in DLS. Also marked expressions of MMP-3 is noted with reddish stains.

Fig. 4
(A,B) Expression of MMP-3 in intervertebral disc of various spinal disease. More thick band expressed in DLS than SS. Sparse expression shows in HNP

Fig. 5
Expression of MMP-3 in intervertebral disc of various spinal disease. Intensity of the bands is evaluated using Image Master VDS software and standardized for β-actin expression. HNP: Herniated Nucleus Pulposus, SS: Spinal Stenosis, DLS: Degenerative Lumbar Scoliosis *: P<0.05.

Fig. 6
RT-PCR amplication of MMP-3 mRNA in the human intervertebral disc which are excised from DLS, SS and HNP. The photograph of 1% agarose gel eletrophoresis shows the gene expression of MMP-3 and GAPDH as single bands of expected sizes in each specimen. and Paragraphs show comparison of gene expression levels of MMP-3 between HNP, SS and DLS. (HNP; Herniated nucleus pulposus, SS: Spinal Stenosis, DLS: Degenerative Lumbar Scoliosis)

Tables

Table 1
Demographics of the samples

Table 2
Sequence of primers

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