Abstract
Background: Low back pain due to disc degeneration is a major problem in industrialized countries. So far surgical treatment has consisted of either fusing the involved segments or replacing them with a prosthetic disc. Both techniques yield unpredictable results.
Objective: Looking at a biological solution we have been exploring the possibilities of harvesting and culturing adult and fetal human intervertebral disc cells in vitro.
Methods: Nucleus pulposus tissue has been surgically removed in cases of scoliosis, lumbar disc degeneration and cervical disc herniation after obtaining patient’s consent. Fetal disc tissue was also obtained following approval by the hospital ethics committee. Tissue was put in culture with and without prior collagenase II digestion. No antibiotics or growth factors were used. Cells were kept in culture until confluence and preserved in liquid nitrogen for further study.
Results: We found that it was possible to obtain homogenous populations of cells macroscopically identifiable as chondrocytes from the adult donnors. Collagenase II treatment provided the best results in adult cells whereas digestion was not necessary for the fetal tissue. The latter showed rapid growth compared to adult cells. Further characterization is underway.
Conclusions: It is possible to obtain cultures of nucleus pulposus human cells from a variety of donors, including adolescent patients with little degeneration as well as from patients showing symptoms and signs of lumbar and cervical disc degeneration.. Fetal tissue could also be cultured without growth factor use. Fetal cells in particular multiplied faster than adult cells and could possibly be used as a cell bank in view of tissue engineering projects.
Theses abstracts were prepared by Professor Roger Lemaire. Correspondence should be addressed to EFORT Central Office, Freihofstrasse 22, CH-8700 Küsnacht, Switzerland.
