Challenges in vascular tissue engineering for diabetic patients

被引:16
作者
Dhulekar, Jhilmil [1 ]
Simionescu, Agneta [1 ]
机构
[1] Clemson Univ, Dept Bioengn, 301 Rhodes Hall, Clemson, SC 29634 USA
基金
美国国家卫生研究院;
关键词
Biological scaffolds; Advanced glycation end products; Mesenchymal stem cells; Antioxidants; MESENCHYMAL STEM-CELLS; PERIPHERAL ARTERIAL-DISEASE; ADIPOSE-DERIVED CELLS; SMOOTH-MUSCLE-CELLS; CORONARY-ARTERY; STROMAL CELLS; CARDIOVASCULAR-DISEASE; EXTRACELLULAR-MATRIX; PROGENITOR CELLS; BLOOD-VESSELS;
D O I
10.1016/j.actbio.2018.01.008
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Hyperglycemia and dyslipidemia coexist in diabetes and result in inflammation, degeneration, and impaired tissue remodeling, processes which are not conducive to the desired integration of tissue engineered products into the surrounding tissues. There are several challenges for vascular tissue engineering such as non-thrombogenicity, adequate burst pressure and compliance, suturability, appropriate remodeling responses, and vasoactivity, but, under diabetic conditions, an additional challenge needs to be considered: the aggressive oxidative environment generated by the high glucose and lipid concentrations that lead to the formation of advanced glycation end products (AGES) in the vascular wall. Extracellular matrix based scaffolds have adequate physical properties and are biocompatible, however, these scaffolds are altered in diabetes by the formation AGEs and impaired collagen degradation, consequently increasing vascular wall stiffness. In addition, vascular cells detect and respond to altered stimuli from the matrix by pathological remodeling of the vascular wall. Due to the immunomodulatory effects of mesenchymal stem cells (MSCs), they are frequently used in tissue engineering in order to protect the scaffolds from inflammation. MSCs together with antioxidant treatments of the scaffolds are expected to protect the vascular grafts from diabetes-induced alterations. In conclusion, as one of the most daunting environments that could damage the ECM and its interaction with cells is progressively built in diabetes, we recommend that cells and scaffolds used in vascular tissue engineering for diabetic patients are tested in diabetic animal models, in order to obtain valuable results regarding their resistance to diabetic adversities. Statement of Significance Almost 25 million Americans have diabetes, characterized by high levels of blood sugar that binds to tissues and disturbs the function of cardiovascular structures. Therefore, patients with diabetes have a high risk of cardiovascular diseases. Surgery is required to replace diseased arteries with implants, but these fail after 5-10 years because they are made of non-living materials, not resistant to diabetes. New tissue engineering materials are developed, based on the patients' own stem cells, isolated from fat, and added to extracellular matrix-based scaffolds. Our main concern is that diabetes could damage the tissue-like implants. Thus we review studies related to the effect of diabetes on tissue components and recommend antioxidant treatments to increase the resistance of implants to diabetes. (C) 2018 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:25 / 34
页数:10
相关论文
共 148 条
[31]  
Chuang TH, 2009, TISSUE ENG PT A, V15, P2837, DOI [10.1089/ten.tea.2008.0394, 10.1089/ten.TEA.2008.0394]
[32]  
Clark N, 2003, DIABETES CARE, V26, P3333
[33]   Purification and long-term culture of multipotent progenitor cells affiliated with the walls of human blood vessels:: Myoendothelial cells and Pericytes [J].
Crisan, Mihaela ;
Deasy, Bridget ;
Gavina, Manuela ;
Zheng, Bo ;
Huard, Johnny ;
Lazzari, Lorenza ;
Peault, Bruno .
STEM CELL CULTURE, 2008, 86 :295-309
[34]   Stem Cell-Containing Hyaluronic Acid-Based Spongy Hydrogels for Integrated Diabetic Wound Healing [J].
da Silva, Lucilia Pereira ;
Santos, Tircia Carlos ;
Rodrigues, Daniel Barreira ;
Pirraco, Rogerio Pedro ;
Cerqueira, Mariana Teixeira ;
Reis, Rui Luis ;
Correlo, Vitor Manuel ;
Marques, Alexandra Pinto .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2017, 137 (07) :1541-1551
[35]   Mesenchymal progenitor cells differentiate into an endothelial phenotype, enhance vascular density, and improve heart function in a rat cellular cardiomyoplasty model [J].
Davani, S ;
Marandin, A ;
Mersin, N ;
Royer, B ;
Kantelip, B ;
Hervé, P ;
Etievent, JP ;
Kantelip, JP .
CIRCULATION, 2003, 108 (10) :253-258
[36]   Toward Development of iMesenchymal Stem Cells for immunomodulatory Therapy [J].
de Witte, Samantha F. H. ;
Franquesa, Marcella ;
Baan, Carla C. ;
Hoogduijn, Martin J. .
FRONTIERS IN IMMUNOLOGY, 2016, 6
[37]  
DelaRosa O, 2009, TISSUE ENG PT A, V15, P2795, DOI 10.1089/ten.TEA.2008.0630
[38]  
Di Marco Elyse, 2013, Front Endocrinol (Lausanne), V4, P68, DOI 10.3389/fendo.2013.00068
[39]   Tissue engineering applications to vascular bypass graft development: The use of adipose-derived stem cells [J].
DiMuzio, Paul ;
Tulenko, Thomas .
JOURNAL OF VASCULAR SURGERY, 2007, 45 :99A-103A
[40]   Hyaluronidase 1 Deficiency Preserves Endothelial Function and Glycocalyx Integrity in Early Streptozotocin-Induced Diabetes [J].
Dogne, Sophie ;
Rath, Geraldine ;
Jouret, Francois ;
Caron, Nathalie ;
Dessy, Chantal ;
Flamion, Bruno .
DIABETES, 2016, 65 (09) :2742-2753