Development of an Organ Culture System for Long-Term Survival of the Intact Human Intervertebral Disc

被引:79
作者
Gawri, Rahul [1 ,2 ]
Mwale, Fackson [2 ]
Ouellet, Jean [3 ]
Roughley, Peter J. [4 ]
Steffen, Thomas [1 ]
Antoniou, John [2 ]
Haglund, Lisbet [1 ]
机构
[1] McGill Univ, Orthopaed Res Lab, Royal Victoria Hosp, Montreal, PQ H3A 1A1, Canada
[2] McGill Univ, Jewish Gen Hosp, Lady Davis Inst Med Res, Montreal, PQ H3A 1A1, Canada
[3] McGill Univ, McGill Scoliosis & Spine Ctr, Montreal, PQ H3A 1A1, Canada
[4] McGill Univ, Shriners Hosp Children, Montreal, PQ H3A 1A1, Canada
关键词
degeneration; human; intervertebral disc; organ culture; repair; IN-VITRO; EXTRACELLULAR-MATRIX; DYNAMIC COMPRESSION; NUCLEUS PULPOSUS; DIURNAL CHANGES; END-PLATE; TRANSPORT; CARTILAGE; GROWTH; DEGENERATION;
D O I
10.1097/BRS.0b013e3181f81314
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Study Design. Human intervertebral discs were used to develop an intact whole disc organ culture system with long-term cell viability. Objective. To develop and validate a long-term organ culture system for intact human intervertebral discs, in which the potential for biologic repair of disc degeneration can be studied. Summary of Background Data. Intervertebral disc degeneration is a common cause of back pain, which can be costly to the health care system and have a negative impact on the quality of life of the patient. Once injured the adult human intervertebral disc seems incapable of intrinsic repair, but the early stages of disc degeneration can potentially be retarded or even reversed by the administration of growth factors to promote new extracellular matrix synthesis. Methods. Intervertebral discs were prepared by three isolation techniques and placed in free swelling organ culture. Cell viability, disc swelling, glycosaminoglycan content, and extracellular matrix degradation were assessed under a variety of culture conditions. Results. Human intervertebral discs isolated with intact cartilage end plates retained cell viability and did not undergo matrix degradation when cultured for 4 weeks with both a high and low nutrient level. This contrasted with the excessive cell death that was observed if the cartilage end plates were removed before culture or if vertebral bone was retained. Conclusion. Retention of the cartilage end plates limits tissue swelling and permits efficient nutrient supply, thus allowing viable long-term organ culture. The availability of such a system will permit the repair potential of therapeutic candidates to be studied in human discs with naturally occurring degeneration. Furthermore, the system is simple and economical, as no apparatus is needed to limit the detrimental effects of excessive tissue swelling.
引用
收藏
页码:1835 / 1842
页数:8
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