CROSSLINKER CONCENTRATION CONTROLS TGFβ-3 RELEASE AND ANNULUS FIBROSUS CELL APOPTOSIS IN GENIPIN-CROSSLINKED FIBRIN HYDROGELS

被引:17
|
作者
Panebianco, C. J. [1 ]
DiStefano, T. J. [1 ]
Mui, B. [1 ]
Hom, W. W. [1 ]
Iatridis, J. C. [1 ]
机构
[1] Icahn Sch Med Mt Sinai, Leni & Peter W May Dept Orthopaed, New York, NY 10029 USA
关键词
Intervertebral disc; annulus fibrosus repair; injectable biomaterials; hydrogel; cell delivery; growth factor delivery; fibrin; genipin crosslinking; apoptosis; musculoskeletal tissue engineering; MESENCHYMAL STEM-CELLS; INTERVERTEBRAL DISC DEGENERATION; LOW-BACK-PAIN; NUCLEUS PULPOSUS; LUMBAR DISKECTOMY; RISK-FACTORS; NONOPERATIVE TREATMENT; IN-VITRO; HERNIATION; REPAIR;
D O I
10.22203/eCM.v039a14
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Back pain is a leading cause of global disability associated with intervertebral disc (IVD) pathologies. Discectomy alleviates disabling pain caused by IVD herniation without repairing annulus fibrosus (AF) defects, which can cause accelerated degeneration and recurrent pain. Biological therapies show promise for IVD repair but developing high-modulus biomaterials capable of providing biomechanical stabilisation and delivering biologics remains an unmet challenge. The present study identified critical factors and developed an optimal formulation to enhance the delivery of AF cells and transforming growth factor beta-3 (TGF beta-3) in genipin-crosslinked fibrin (FibGen) hydrogels. Part 1 showed that AF cells encapsulated in TGF beta-3-supplemented high-modulus FibGen synthesised little extracellular matrix (ECM) but could release TGF beta-3 at physiologically relevant levels. Part 2 showed that AF cells underwent apoptosis when encapsulated in FibGen, even after reducing fibrin concentration from 70 to 5 mg/mL. Mechanistic experiments, modifying genipin concentration and integrin binding site presence demonstrated that genipin crosslinking caused AF cell apoptosis by inhibiting cell-biomaterial binding. Adding integrin binding sites with fibronectin partially rescued apoptosis, indicating genipin also caused acute cytotoxicity. Part 3 showed that FibGen formulations with 1 mg/mL genipin had enhanced ECM synthesis when supplemented with fibronectin and TGF beta-3. In conclusion, FibGen could be used for delivering biologically active compounds and AF cells, provided that formulations supplied additional sites for cell-biomaterial binding and genipin concentrations were low. Results also highlighted a need for developing strategies that protect cells against acute crosslinker cytotoxicity to overcome challenges of engineering high-modulus cell carriers for musculoskeletal tissues that experience high mechanical demands.
引用
收藏
页码:211 / 226
页数:16
相关论文
共 3 条
  • [1] GENIPIN-CROSSLINKED FIBRIN HYDROGELS MODIFIED WITH COLLAGEN OR FIBRONECTIN AS AN ANNULUS FIBROSUS SEALANT
    Guterl, Clare Canal
    Kim, Tyler
    Nicoll, Steven B.
    Iatridis, James C.
    PROCEEDINGS OF THE ASME SUMMER BIOENGINEERING CONFERENCE, PTS A AND B, 2012, : 1151 - 1152
  • [2] GENIPIN-CROSSLINKED FIBRIN HYDROGELS AS A POTENTIAL ADHESIVE TO AUGMENT INTERVERTEBRAL DISC ANNULUS REPAIR
    Schek, R. M.
    Michalek, A. J.
    Iatridis, J. C.
    EUROPEAN CELLS & MATERIALS, 2011, 21 : 373 - 383
  • [3] Genipin-crosslinked decellularized annulus fibrosus hydrogels induces tissue-specific differentiation of bone mesenchymal stem cells and intervertebral disc regeneration
    Peng, Yizhong
    Huang, Donghua
    Li, Jinye
    Liu, Sheng
    Qing, Xiangcheng
    Shao, Zengwu
    JOURNAL OF TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2020, 14 (03) : 497 - 509