A Preliminary Study of Placental Acellular Matrix as Tissue Repair Material

被引:0
|
作者
Liu Xiu [1 ]
Zang Chuan-Bao [1 ]
Lin Yan-Chao [1 ]
Cheng Long [1 ]
Fu Xiao-Meng [1 ]
机构
[1] Yinfeng Cryomed Technol CO Ltd, Jinan 250102, Peoples R China
关键词
placenta; acellular matrix; biomaterials; umbilical cord mesenchymal stem cells; MESENCHYMAL STEM-CELLS; EXTRACELLULAR-MATRIX; DECELLULARIZATION; STRATEGIES; GRAFT;
D O I
10.16476/j.pibb.2021.0343
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Objective To prepare and evaluate the biocompatibility of placental acellular matrix and to explore its feasibility as tissue repair material. Methods The waste placental tissue from delivery was handled by virus inactivation, acellular treatment and freeze-drying to obtain the acellular spongy matrix material of placenta. The effect of acellular was observed by HE staining and the microstructure of the materials was observed by scanning electron microscope. At the same time, 39 healthy male SD rats with body mass ranging from 120 g to 150 g were selected, randomly divided into experiment 1 group, experiment 2 group and control group. The subcutaneous implantation of the constructed matrix material was performed in rats, experimental group 1 implanted matrix materials, experimental group 2 implanted matrix materials and umbilical cord mesenchymal stem cells, the control group was the sham operation group. Routine blood tests were performed on the 3rd, 5th and 7th day after surgery to analyze the number of lymphocytes, granulocytes and other inflammatory cells. At 1, 2, 4, 8 and 9 week after the operation, the tissue samples of the implanted material and surrounding tissues were taken for HE staining analysis. Results The constructed acellular matrix of placenta appears milky white spongy in macroscopic view, HE staining indicated no cell residue. Under electron microscope, the internal void of the material was obvious, and the crosslinking degree of the material was good. The total porosity was (77.54 +/- 2.53)%. After subcutaneous implantation, the incision healed well, and no obvious inflammatory cell increase was observed in blood routine examination. Seven days after the operation, blood vessel formation can be observed by HE staining in the sections of the implanted materials. Moreover, the addition of umbilical cord mesenchymal stem cells can accelerate the fusion of the materials with the body, promote the in-depth growth of cells and vascularization. Conclusion Placental acellular sponge matrix material has good biocompatibility and can be an ideal source of tissue engineering materials.
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页码:2034 / 2040
页数:7
相关论文
共 28 条
  • [1] Laterally positioned flap along with acellular dermal matrix graft in the management of maxillary localized recessions
    Ahmedbeyli, Cavid
    Ipci, Sebnem Dirikan
    Cakar, Gokser
    Yilmaz, Selcuk
    [J]. CLINICAL ORAL INVESTIGATIONS, 2019, 23 (02) : 595 - 601
  • [2] RETRACTED: Engineered whole organs and complex tissues (Retracted article. See vol. 392, pg. 11, 2018)
    Badylak, Stephen F.
    Weiss, Daniel J.
    Caplan, Arthur
    Macchiarini, Paolo
    [J]. LANCET, 2012, 379 (9819): : 943 - 952
  • [3] Extracellular matrix as a biological scaffold material: Structure and function
    Badylak, Stephen F.
    Freytes, Donald O.
    Gilbert, Thomas W.
    [J]. ACTA BIOMATERIALIA, 2009, 5 (01) : 1 - 13
  • [4] Endothelial differentiation of Wharton's jelly-derived mesenchymal stem cells in comparison with bone marrow-derived mesenchymal stem cells
    Chen, Ming-Yan
    Lie, Pu-Chang
    Li, Zhi-Ling
    Wei, Xing
    [J]. EXPERIMENTAL HEMATOLOGY, 2009, 37 (05) : 629 - 640
  • [5] Decellularized zebrafish cardiac extracellular matrix induces mammalian heart regeneration
    Chen, William C. W.
    Wang, Zhouguang
    Missinato, Maria Azzurra
    Park, Dae Woo
    Long, Daniel Ward
    Liu, Heng-Jui
    Zeng, Xuemei
    Yates, Nathan A.
    Kim, Kang
    Wang, Yadong
    [J]. SCIENCE ADVANCES, 2016, 2 (11):
  • [6] Mesenchymal stem cells as a potential pool for cartilage tissue engineering
    Csaki, C.
    Schneider, P. R. A.
    Shakibaei, M.
    [J]. ANNALS OF ANATOMY-ANATOMISCHER ANZEIGER, 2008, 190 (05) : 395 - 412
  • [7] Daley George Q, 2003, Hematology Am Soc Hematol Educ Program, P398
  • [8] Role of the Extracellular Matrix in Whole Organ Engineering
    Faulk, Denver M.
    Johnson, Scott A.
    Zhang, Li
    Badylak, Stephen F.
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 2014, 229 (08) : 984 - 989
  • [9] Perfusion decellularization of whole organs
    Guyette, Jacques P.
    Gilpin, Sarah E.
    Charest, Jonathan M.
    Tapias, Luis F.
    Ren, Xi
    Ott, Harald C.
    [J]. NATURE PROTOCOLS, 2014, 9 (06) : 1451 - 1468
  • [10] Evaluation of adult equine bone marrow- and adipose-derived progenitor cell chondrogenesis in hydrogel cultures
    Kisiday, John D.
    Kopesky, Paul W.
    Evans, Christopher H.
    Grodzinsky, Alan J.
    McIlwraith, C. Wayne
    Frisbie, David D.
    [J]. JOURNAL OF ORTHOPAEDIC RESEARCH, 2008, 26 (03) : 322 - 331