Abstract.
Transforming growth factor β (TGF-β) is a potent inducer of angiogenesis and fibrogenesis. There is presently little information about the pathophysiological function of TGF-β in herniated disc tissue. In order to analyze the cellular role and activation of TGF-β after disc herniation we immunostained frozen material from 38 disc herniation operations and from eight macroscopically normal discs from organ donors. Polyclonal TGF-β-I, TGF-β-II and TGF-β receptor type II antibodies were used with the avidin biotin complex (ABC-) immunoperoxidase method. All the herniated discs were TGF-β immunopositive. Such immunoreactivity was mainly associated with disc cells. In a few samples, capillaries were also TGF-β immunopositive. Immunopositivity was similarly observed in the control discs. To analyze possible differences between the two groups, we calculated the ratio of immunopositive disc cells. For all three antibodies, a statistically significantly (Mann-Whitney test, P=0.0001) higher number of disc cells showed immunopositivity in the herniated discs. The increase in TGF-β receptor immunopositivity suggested induction of TGF-β receptors in herniated discs. Our results support an active regulatory role for TGF-β in disc cell metabolism.
Keywords: Herniated disc TGF-β
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