Microgel Microenvironment Primes Adipose-Derived Stem Cells Towards an NP Cells-Like Phenotype

被引:39
作者
Fontana, Gianluca [1 ]
Thomas, Dilip [1 ]
Collin, Estelle [1 ]
Pandit, Abhay [1 ]
机构
[1] Natl Univ Ireland, Network Excellence Funct Biomat, Galway, Ireland
关键词
NUCLEUS PULPOSUS CELLS; COLLAGEN TYPE-II; LOW-BACK-PAIN; INTERVERTEBRAL DISC DEGENERATION; EXTRACELLULAR-MATRIX; CHONDROGENIC DIFFERENTIATION; GENE-THERAPY; IN-VITRO; CHONDROCYTE DIFFERENTIATION; SOX9; EXPRESSION;
D O I
10.1002/adhm.201400175
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Cell therapy of the degenerated intervertebral disc is limited by the lack of appropriate cell sources, thus new strategies for the differentiation of stem cells towards a nucleus pulposus (NP)-like phenotype need investigation. In the current study, it is hypothesized that spherical niche-like structures composed of type II collagen and hyaluronan (HA) mimic the NP microenvironment and promote the differentiation of adipose-derived stem cells (ADSCs) towards an NP-like phenotype. ADSCs are embedded in microgels of different concentrations of collagen II/HA. Cells' response to the different environments is studied by characterizing differences in cells' viability, morphology, and gene expression. After 21 days of culture, ADSCs maintain +/- 80% viability in all the conditions tested. Moreover, microgels with higher concentration of collagen are stable and maintain cells in a rounder shape. In presence of differentiation media, cells are able to differentiate in all the conditions tested, but in a more pronounced manner in the microgel with a higher concentration of collagen. By tuning microgels' properties, it is possible to influence ADSCs' phenotype and ability to differentiate. Indeed, when cultured in high concentrations of collagen, ADSCs expresses high levels of collagen II, aggrecan, SOX9, and low levels of collagen I.
引用
收藏
页码:2012 / 2022
页数:11
相关论文
共 85 条
  • [21] Gruber H. E., 2000, BMC MUSCULOSKEL DIS, V1, P23
  • [22] Guterl CC, 2013, EUR CELLS MATER, V25, P1
  • [23] Hakkinen KM, 2011, TISSUE ENG PT A, V17, P713, DOI [10.1089/ten.tea.2010.0273, 10.1089/ten.TEA.2010.0273]
  • [24] The Postnatal Role of Sox9 in Cartilage
    Henry, Stephen P.
    Liang, Shoudan
    Akdemir, Kadir C.
    de Crombrugghe, Benoit
    [J]. JOURNAL OF BONE AND MINERAL RESEARCH, 2012, 27 (12) : 2511 - 2525
  • [25] The Epidemiology of low back pain
    Hoy, D.
    Brooks, P.
    Blyth, F.
    Buchbinder, R.
    [J]. BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY, 2010, 24 (06): : 769 - 781
  • [26] Huebsch N, 2010, NAT MATER, V9, P518, DOI [10.1038/nmat2732, 10.1038/NMAT2732]
  • [27] Regulation of osteogenic and chondrogenic differentiation of mesenchymal stem cells in PEG-ECM hydrogels
    Hwang, Nathaniel S.
    Varghese, Shyni
    Li, Hanwei
    Elisseeff, Jennifer
    [J]. CELL AND TISSUE RESEARCH, 2011, 344 (03) : 499 - 509
  • [28] Strategies for regeneration of the intervertebral disc
    Kalson, N. S.
    Richardson, S.
    Hoyland, J. A.
    [J]. REGENERATIVE MEDICINE, 2008, 3 (05) : 717 - 729
  • [29] Lumbar disc disorders and low-back pain: Socioeconomic factors and consequences
    Katz, JN
    [J]. JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2006, 88A : 21 - 24
  • [30] Intervertebral Disk Degeneration and Emerging Biologic Treatments
    Kepler, Christopher K.
    Anderson, D. Greg
    Tannoury, Chadi
    Ponnappan, Ravi K.
    [J]. JOURNAL OF THE AMERICAN ACADEMY OF ORTHOPAEDIC SURGEONS, 2011, 19 (09) : 543 - 553