Fibrosis in tissue engineering and regenerative medicine: treat or trigger?

被引:20
作者
Fernandez-Colino, Alicia [1 ]
Iop, Laura [2 ]
Ferreira, Monica S. Ventura [3 ]
Mela, Petra [1 ,4 ]
机构
[1] Rhein Westfal TH Aachen, Helmholtz Inst, AME Inst Appl Med Engn, Dept Biohybrid & Med Text BioTex, Forckenbeckstr 55, D-52074 Aachen, Germany
[2] Univ Padua, Dept Cardiac Thorac Vasc Sci & Publ Hlth, Pietro dAbano Biomed Campus,Via G Orus 2, I-35129 Padua, Italy
[3] Rhein Westfal TH Aachen, Dept Haematol Oncol Haemostaseol & Stem Cell Tran, Pauwelsstr 30, D-52074 Aachen, Germany
[4] Tech Univ Munich, Dept Mech Engn, Med Mat & Implants, Boltzmannstr 15, D-85748 Garching, Germany
关键词
Tissues and organs; Heart; Kidney; Lung; Liver; Disease models; Cell and material-based therapies; MESENCHYMAL STEM-CELLS; IDIOPATHIC PULMONARY-FIBROSIS; ELEVATION MYOCARDIAL-INFARCTION; VENTRICULAR OUTFLOW TRACT; PIVOTAL PRECLINICAL TRIAL; CHRONIC KIDNEY-DISEASE; LIVER SUPPORT-SYSTEMS; BONE-MARROW ORIGIN; 3D CULTURE-SYSTEMS; IN-VITRO MODELS;
D O I
10.1016/j.addr.2019.07.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Fibrosis is a life-threatening pathological condition resulting from a dysfunctional tissue repair process. There is no efficient treatment and organ transplantation is in many cases the only therapeutic option. Here we review tissue engineering and regenerative medicine (TERM) approaches to address fibrosis in the cardiovascular system, the kidney, the lung and the liver. These strategies have great potential to achieve repair or replacement of diseased organs by cell- and material-based therapies. However, paradoxically, they might also trigger fibrosis. Cases of TERM interventions with adverse outcome are also included in this review. Furthermore, we emphasize the fact that, although organ engineering is still in its infancy, the advances in the field are leading to biomedically relevant in vitro models with tremendous potential for disease recapitulation and development of therapies. These human tissue models might have increased predictive power for human drug responses thereby reducing the need for animal testing. (C) 2019 Published by Elsevier B.V.
引用
收藏
页码:17 / 36
页数:20
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