Localization of cathepsins D, K, and L in degenerated human intervertebral discs

• Published in: Spine (Philadelphia, Pa. 1976) Pa. 1976), 2001-12, Vol.26 (24), p.2666-2672
• Main Authors: ARIGA, Kenta, YONENOBU, Kazuo, NAKASE, Takanobu, KANEKO, Motoharu, OKUDA, Sin'Ya, UCHIYAMA, Yasuo, YOSHIKAWA, Hideki
• Format: Article
• Language: English
• Subjects: Adult; Aged; Aged, 80 and over; Biological and medical sciences; Cathepsin D - metabolism; Cathepsin K; Cathepsin L; Cathepsins - metabolism; Cysteine Endopeptidases; Diseases of the osteoarticular system; Diseases of the spine; Female; Humans; Immunohistochemistry; Intervertebral Disc - metabolism; Intervertebral Disc - pathology; Male; Medical sciences; Middle Aged
• ISSN: 0362-2436; 1528-1159
• DOI: 10.1097/00007632-200112150-00007

Localization of cathepsins D, K, and L in degenerated intervertebral discs was examined by immunohistochemistry. To determine the involvement of cathepsins in the pathomechanism of intervertebral disc degeneration by monitoring the immunolocalization of cathepsins in degenerated intervertebral disc tissue. Cathepsins D, K, and L are enzymes that contribute to the matrix destruction seen in the articular cartilage affected by osteoarthritis and rheumatoid arthritis. However, little is known about the contribution of these cathepsins to intervertebral disc degeneration. Paraffin-embedded sections of degenerated intervertebral disc tissue collected at the time of surgery (13 discs from 12 patients) were immunohistochemically stained with antibodies for cathepsins D, K, and L. For further characterization of the stained cells, immunohistochemical detection of CD68 and TRAP staining were performed. Hematoxylin and eosin staining revealed obvious signs of degeneration in all sections. Cathepsins D and L were immunolocalized in disc fibrochondrocytes at various sites exhibiting degeneration. Cathepsins K were found in tartrate-resistant acid phosphatase-positive multinucleated cells, in particular near the cleft within the cartilaginous endplate. However, few cells were positive for these cathepsins in anulus fibrosus that maintained the lamellar structure of collagen fibers. Marked expression of cathepsins D and L was observed at the site of degeneration. Cathepsins D and K localized in tartrate-resistant acid phosphatase-positive multinucleated cells existed at the cleft between the cartilaginous endplate and vertebral body. The site-specific localization of these cathepsins suggests the association of these proteinases with endplate separation and disorganization of the anulus fibrosus in degenerative spinal disorders.