Amnion Membrane Hydrogel and Amnion Membrane Powder Accelerate Wound Healing in a Full Thickness Porcine Skin Wound Model

被引:64
作者
Murphy, Sean, V [1 ]
Skardal, Aleksander [1 ]
Nelson, Ronald A., Jr. [1 ]
Sunnon, Khiry [1 ]
Reid, Tanya [1 ]
Clouse, Cara [1 ]
Kock, Nancy D. [2 ]
Jackson, John [1 ]
Soker, Shay [1 ]
Atala, Anthony [1 ]
机构
[1] Wake Forest Sch Med, Wake Forest Inst Regenerat Med, Med Ctr Blvd, Winston Salem, NC 27101 USA
[2] Wake Forest Sch Med, Dept Pathol Comparat Med, Med Ctr Blvd, Winston Salem, NC USA
关键词
Amnion membrane; Hydrogel; Amnion powder; Skin; Wound; Extracellular matrix; REGENERATIVE TISSUE MATRIX; MANAGEMENT; BURNS; IMMUNOSUPPRESSION; BIOBRANE;
D O I
10.1002/sctm.19-0101
中图分类号
Q813 [细胞工程];
学科分类号
摘要
There is a need for effective wound treatments that retain the bioactivity of a cellular treatment, but without the high costs and complexities associated with manufacturing, storing, and applying living biological products. Previously, we developed an amnion membrane-derived hydrogel and evaluated its wound healing properties using a mouse wound model. In this study, we used a full thickness porcine skin wound model to evaluate the wound-healing efficacy of the amnion hydrogel and a less-processed amnion product comprising a lyophilized amnion membrane powder. These products were compared with commercially available amnion and nonamnion wound healing products. We found that the amnion hydrogel and amnion powder treatments demonstrated significant and rapid wound healing, driven primarily by new epithelialization versus closure by contraction. Histological analysis demonstrated that these treatments promote the formation of a mature epidermis and dermis with similar composition to healthy skin. The positive skin regenerative outcomes using amnion hydrogel and amnion powder treatments in a large animal model further demonstrate their potential translational value for human wound treatments. Stem Cells Translational Medicine 2019
引用
收藏
页码:80 / 92
页数:13
相关论文
共 43 条
[1]   Mechanical load initiates hypertrophic scar formation through decreased cellular apoptosis [J].
Aarabi, Shahram ;
Bhatt, Kirit A. ;
Shi, Yubin ;
Paterno, Josemaria ;
Chang, Edward I. ;
Loh, Shang A. ;
Holmes, Jeffrey W. ;
Longaker, Michael T. ;
Yee, Herman ;
Gurtner, Geoffrey C. .
FASEB JOURNAL, 2007, 21 (12) :3250-3261
[2]  
ALEXANDER JW, 1981, J TRAUMA, V21, P433
[3]   USE AND USES OF LARGE SPLIT SKIN GRAFTS OF INTERMEDIATE THICKNESS [J].
BLAIR, VP ;
BROWN, JB .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1968, 42 (01) :65-+
[4]   Arthroscopic replacement of massive, irreparable rotator cuff tears using a GraftJacket allograft: Technique and preliminary results [J].
Bond, James L. ;
Dopirak, Ryan M. ;
Higgins, Jason ;
Burns, Joseph ;
Snyder, Stephen J. .
ARTHROSCOPY-THE JOURNAL OF ARTHROSCOPIC AND RELATED SURGERY, 2008, 24 (04) :403-409
[5]  
BOSE B, 1979, ANN ROY COLL SURG, V61, P444
[6]   Amnion in the treatment of pediatric partial-thickness facial burns [J].
Branski, Ludwik K. ;
Herndon, David N. ;
Celis, Mario M. ;
Norbury, William B. ;
Masters, Oscar E. ;
Jeschke, Marc G. .
BURNS, 2008, 34 (03) :393-399
[7]  
Brigido SA, 2004, ORTHOPEDICS, V27, pS145
[8]   IMMUNOSUPPRESSION AND TEMPORARY SKIN TRANSPLANTATION IN TREATMENT OF MASSIVE 3RD DEGREE BURNS [J].
BURKE, JF ;
QUINBY, WC ;
BONDOC, CC ;
COSIMI, AB ;
RUSSELL, PS ;
SZYFELBEIN, SK .
ANNALS OF SURGERY, 1975, 182 (03) :183-197
[9]  
Cornwell Kevin G, 2009, Clin Podiatr Med Surg, V26, P507, DOI 10.1016/j.cpm.2009.08.001
[10]  
Davis JS., 1910, Johns Hopkins Med J, V15, P307, DOI DOI 10.1097/00000658-190909000-00022