Sulfated Hydrogels as Primary Intervertebral Disc Cell Culture Systems

被引:2
作者
Bermudez-Lekerika, Paola [1 ,2 ]
Crump, Katherine B. [1 ,2 ]
Wuertz-Kozak, Karin [3 ,4 ]
Le Maitre, Christine L. [5 ]
Gantenbein, Benjamin [1 ,6 ]
机构
[1] Univ Bern, Med Fac, Dept Biomed Res DBMR, Tissue Engn Orthopaed & Mechanobiol Bone & Joint P, CH-3008 Bern, Switzerland
[2] Univ Bern, Grad Sch Cellular & Biomed Sci GCB, CH-3012 Bern, Switzerland
[3] Rochester Inst Technol, Dept Biomed Engn, Rochester, NY 14623 USA
[4] Paracelsus Private Med Univ Salzburg Austria, Schon Klin Munchen Harlaching Acad Teaching Hosp, Spine Res Inst, Spine Ctr, D-81547 Munich, Germany
[5] Univ Sheffield, Sch Med & Populat Hlth, Div Clin Med, Sheffield S10 2TN, England
[6] Univ Bern, Med Fac, Dept Orthoped Surg & Traumatol, Inselspital, CH-3010 Bern, Switzerland
关键词
intervertebral disc; sulfation alginate; 3D culture; qPCR; cell viability; LOW-BACK-PAIN; ALGINATE HYDROGELS; IN-VITRO; DEGENERATION; REGENERATION; DIFFERENTIATION; CHONDROGENESIS; PROLIFERATION; ACTIVATION; EXPRESSION;
D O I
10.3390/gels10050330
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The negatively charged extracellular matrix plays a vital role in intervertebral disc tissues, providing specific cues for cell maintenance and tissue hydration. Unfortunately, suitable biomimetics for intervertebral disc regeneration are lacking. Here, sulfated alginate was investigated as a 3D culture material due to its similarity to the charged matrix of the intervertebral disc. Precursor solutions of standard alginate, or alginate with 0.1% or 0.2% degrees of sulfation, were mixed with primary human nucleus pulposus cells, cast, and cultured for 14 days. A 0.2% degree of sulfation resulted in significantly decreased cell density and viability after 7 days of culture. Furthermore, a sulfation-dependent decrease in DNA content and metabolic activity was evident after 14 days. Interestingly, no significant differences in cell density and viability were observed between surface and core regions for sulfated alginate, unlike in standard alginate, where the cell number was significantly higher in the core than in the surface region. Due to low cell numbers, phenotypic evaluation was not achieved in sulfated alginate biomaterial. Overall, standard alginate supported human NP cell growth and viability superior to sulfated alginate; however, future research on phenotypic properties is required to decipher the biological properties of sulfated alginate in intervertebral disc cells.
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页数:16
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