Integration of stem cell-derived exosomes with in situ hydrogel glue as a promising tissue patch for articular cartilage regeneration

被引:468
作者
Liu, Xiaolin [1 ]
Yang, Yunlong [1 ,2 ]
Li, Yan [2 ]
Niu, Xin [1 ]
Zhao, Bizeng [1 ]
Wang, Yang [1 ]
Bao, Chunyan [2 ]
Xie, Zongping [1 ]
Lin, Qiuning [2 ]
Zhu, Linyong [2 ]
机构
[1] Shanghai Jiao Tong Univ, Affiliated People Hosp 6, Inst Microsurg Extrem, Dept Orthopaed Surg, 600 Yishan Rd, Shanghai 200233, Peoples R China
[2] East China Univ Sci & Technol, Inst Fine Chem, Key Lab Adv Mat, 130 Meilong Rd, Shanghai 200237, Peoples R China
关键词
REPAIR; BONE; THERAPIES; DEFECTS; INJURY; VIVO;
D O I
10.1039/c7nr00352h
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
The regeneration of articular cartilage, which scarcely shows innate self-healing ability, is a great challenge in clinical treatment. Stem cell-derived exosomes (SC-Exos), an important type of extracellular nanovesicle, exhibit great potential for cartilage regeneration to replace stem cell-based therapy. Cartilage regeneration often takes a relatively long time and there is currently no effective administration method to durably retain exosomes at cartilage defect sites to effectively exert their reparative effect. Therefore, in this study, we exploited a photoinduced imine crosslinking hydrogel glue, which presents excellent operation ability, biocompatibility and most importantly, cartilage-integration, as an exosome scaffold to prepare an acellular tissue patch (EHG) for cartilage regeneration. It was found that EHG can retain SC-Exos and positively regulate both chondrocytes and hBMSCs in vitro. Furthermore, EHG can integrate with native cartilage matrix and promote cell deposition at cartilage defect sites, finally resulting in the promotion of cartilage defect repair. The EHG tissue patch therefore provides a novel, cell-free scaffold material for wound repair.
引用
收藏
页码:4430 / 4438
页数:9
相关论文
共 36 条
[1]
Stem Cell Therapies for Knee Cartilage Repair The Current Status of Preclinical and Clinical Studies [J].
Anderson, John A. ;
Little, Dianne ;
Toth, Alison P. ;
Moorman, Claude T., III ;
Tucker, Bradford S. ;
Ciccotti, Michael G. ;
Guilak, Farshid .
AMERICAN JOURNAL OF SPORTS MEDICINE, 2014, 42 (09) :2253-2261
[2]
[Anonymous], 2014, J CIRC BIOMARK, DOI DOI 10.5772/58597
[3]
Comparison of the bony ingrowth into an osteochondral defect and an artificial osteochondral composite device in load-bearing joints [J].
Chang, YS ;
Gu, HO ;
Kobayashi, M ;
Oka, M .
KNEE, 1998, 5 (03) :205-213
[4]
Calcification or Dedifferentiation: Requirement to Lock Mesenchymal Stem Cells in a Desired Differentiation Stage [J].
Dickhut, Andrea ;
Pelttari, Karoliina ;
Janicki, Patricia ;
Wagner, Wolfgang ;
Eckstein, Volker ;
Egermann, Marcus ;
Richter, Wiltrud .
JOURNAL OF CELLULAR PHYSIOLOGY, 2009, 219 (01) :219-226
[5]
Regenerating the injured kidney with human umbilical cord mesenchymal stem cell-derived exosomes [J].
Dorronsoro, Akaitz ;
Robbins, Paul D. .
STEM CELL RESEARCH & THERAPY, 2013, 4
[6]
Unlike Bone, Cartilage Regeneration Remains Elusive [J].
Huey, Daniel J. ;
Hu, Jerry C. ;
Athanasiou, Kyriacos A. .
SCIENCE, 2012, 338 (6109) :917-921
[7]
Large-scale generation of cell-derived nanovesicles [J].
Jo, W. ;
Kim, J. ;
Yoon, J. ;
Jeong, D. ;
Cho, S. ;
Jeong, H. ;
Yoon, Y. J. ;
Kim, S. C. ;
Gho, Y. S. ;
Park, J. .
NANOSCALE, 2014, 6 (20) :12056-12064
[8]
CHEMISTRY Repair or Replacement-A Joint Perspective [J].
Klein, Jacob .
SCIENCE, 2009, 323 (5910) :47-48
[9]
Lai RC, 2011, REGEN MED, V6, P481, DOI [10.2217/RME.11.35, 10.2217/rme.11.35]
[10]
3D plasmonic nanobowl platform for the study of exosomes in solution [J].
Lee, Changwon ;
Carney, Randy P. ;
Hazari, Sidhartha ;
Smith, Zachary J. ;
Knudson, Alisha ;
Robertson, Christopher S. ;
Lam, Kit S. ;
Wachsmann-Hogiu, Sebastian .
NANOSCALE, 2015, 7 (20) :9290-9297