K. Miyahara et al., HUMAN GROUP-II PHOSPHOLIPASE A(2) IN NORMAL AND DISEASED INTERVERTEBRAL DISCS, Biochimica et biophysica acta. Molecular basis of disease, 1316(3), 1996, pp. 183-190
We measured calcium-dependent phospholipase A(2) (PLA(2)) activity and
immunoreactive group II PLA(2) levels of 54 normal discs obtained fro
m cadavers and 73 disc samples surgically obtained from patients with
spinal disorders, including intervertebral disc herniations, spondylos
is, and spondylolisthesis. Both cadaveric and surgical disc specimens
contained about two-fold greater PLA(2) activity than the ileal mucosa
, one of the richest sources of group II PLA(2). Discs of middle-aged
cases had significantly higher activity than those of younger and elde
r cases. In cadaveric normal discs, calcium-dependent PLA(2) activity
was significantly higher in females than in males. Annulus fibrosus an
d nucleus pulposus contained the same PLA(2) levels. In diseased discs
, herniated fragments that had extruded or protruded out of the discs
possessed lower activity than other parts of discs in the intervertebr
al space. Immunoreactive group II PLA(2) levels of intervertebral disc
s closely correlated with PLA(2) enzymatic activity. We purified a PLA
(2) from human intervertebral disc to homogeneity to further identify
the isozymic nature of discal PLA(2). Its NH2-terminal amino acid sequ
ence and molecular weight were identical to those of human group II PL
A(2). Immunohistochemical analysis using a monoclonal anti-group II PL
A(2) antibody showed that in both annulus fibrosus and nucleus pulposu
s chondrocytes contained intense group II PLA(2) immunoreactivity in t
heir cytoplasm, and that the matrix contained no substantial immunorea
ctivity. These results suggest that group II PLA(2) in chondrocytes ha
s important physiological roles in discal ordinary metabolism, maintai
ning discal homeostasis.