STUDY DESIGN: Whole ovine caudal intervertebral discs (IVD) were cultured in sufficient and limited nutrition under simulated-physiologic loading for 7 and 21 days. OBJECTIVE: To study the effect of limited nutrition on disc cells embedded in their native tissue in short- and midterm whole organ disc culture. SUMMARY OF BACKGROUND DATA: Nutrient-limited induction of disc cell death in vitro has been demonstrated and is believed to be a factor in disc degeneration. Nutrient-limited cell death and its consequences, as it relates to degeneration, have not been investigated in the intact IVD. METHODS: Ovine IVDs with endplates were cultured for 7 and 21 days under simulated-physiologic loading, either in media with limited (2 g/L) or sufficient (4.5 g/L) glucose concentration. Cell viability, relative gene expression, newly synthesized chondroitin sulfate content, and matrix metalloproteinase (MMP) activity were measured after culture and compared to fresh tissue. RESULTS: In sufficient glucose media, cell viability was maintained through 7 days to 21 days of culture. In limited glucose, it dropped significantly to 62% in the anulus fibrosus and to 56% in the nucleus pulposus after 7 days and remained so until 21 days (63% in the anulus fibrosus and 52% in the nucleus pulposus). No significant differences were found between culture conditions for relative gene expression, newly synthesized chondroitin sulfate and inactive and active forms of MMP13 and MMP7. CONCLUSION: With this culture system, whole IVD explants could be maintained up to 21 days. Cell viability decreased to 50% to 60% under limited nutrition within days and remained so up to 3 weeks. The surviving cells did not compensate matrix production in this time frame.
STUDY DESIGN: Whole ovine caudal intervertebral discs (IVD) were cultured in sufficient and limited nutrition under simulated-physiologic loading for 7 and 21 days. OBJECTIVE: To study the effect of limited nutrition on disc cells embedded in their native tissue in short- and midterm whole organ disc culture. SUMMARY OF BACKGROUND DATA: Nutrient-limited induction of disc cell death in vitro has been demonstrated and is believed to be a factor in disc degeneration. Nutrient-limited cell death and its consequences, as it relates to degeneration, have not been investigated in the intact IVD. METHODS: Ovine IVDs with endplates were cultured for 7 and 21 days under simulated-physiologic loading, either in media with limited (2 g/L) or sufficient (4.5 g/L) glucose concentration. Cell viability, relative gene expression, newly synthesized chondroitin sulfate content, and matrix metalloproteinase (MMP) activity were measured after culture and compared to fresh tissue. RESULTS: In sufficient glucose media, cell viability was maintained through 7 days to 21 days of culture. In limited glucose, it dropped significantly to 62% in the anulus fibrosus and to 56% in the nucleus pulposus after 7 days and remained so until 21 days (63% in the anulus fibrosus and 52% in the nucleus pulposus). No significant differences were found between culture conditions for relative gene expression, newly synthesized chondroitin sulfate and inactive and active forms of MMP13 and MMP7. CONCLUSION: With this culture system, whole IVD explants could be maintained up to 21 days. Cell viability decreased to 50% to 60% under limited nutrition within days and remained so up to 3 weeks. The surviving cells did not compensate matrix production in this time frame.
Authors: Svenja Illien-Jünger; Young Lu; Devina Purmessur; Jillian E Mayer; Benjamin A Walter; Peter J Roughley; Sheeraz A Qureshi; Andrew C Hecht; James C Iatridis Journal: Spine J Date: 2014-04-24 Impact factor: 4.166
Authors: D Purmessur; B A Walter; P J Roughley; D M Laudier; A C Hecht; James Iatridis Journal: Biochem Biophys Res Commun Date: 2013-02-22 Impact factor: 3.575
Authors: Joana C Antunes; Catarina Leite Pereira; Graciosa Q Teixeira; Ricardo V Silva; Joana Caldeira; Sibylle Grad; Raquel M Gonçalves; Mário A Barbosa Journal: J Mater Sci Mater Med Date: 2016-11-24 Impact factor: 3.896
Authors: Benjamin Gantenbein; Svenja Illien-Jünger; Samantha C W Chan; Jochen Walser; Lisbet Haglund; Stephen J Ferguson; James C Iatridis; Sibylle Grad Journal: Curr Stem Cell Res Ther Date: 2015 Impact factor: 3.828
Authors: C C Guterl; E Y See; S B G Blanquer; A Pandit; S J Ferguson; L M Benneker; D W Grijpma; D Sakai; D Eglin; M Alini; J C Iatridis; S Grad Journal: Eur Cell Mater Date: 2013-01-02 Impact factor: 3.942
Authors: M Likhitpanichkul; M Dreischarf; S Illien-Junger; B A Walter; T Nukaga; R G Long; D Sakai; A C Hecht; J C Iatridis Journal: Eur Cell Mater Date: 2014-07-18 Impact factor: 3.942