A Co-Culture System for Studying Cellular Interactions in Vascular Disease

被引:6
作者
Padmanaban, Abirami M. [1 ]
Ganesan, Kumar [2 ]
Ramkumar, Kunka Mohanram [1 ]
机构
[1] SRM Inst Sci & Technol, Sch Bioengn, Dept Biotechnol, Kattankulathur 603203, Tamil Nadu, India
[2] Univ Hong Kong, Li Ka Shing Fac Med, Sch Chinese Med, Pokfulam, 10 Sassoon Rd, Hong Kong 999077, Peoples R China
来源
BIOENGINEERING-BASEL | 2024年 / 11卷 / 11期
关键词
cardiovascular diseases; endothelial dysfunction; co-culture models; cellular interactions; vascular pathology;
D O I
10.3390/bioengineering11111090
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Cardiovascular diseases (CVDs) are leading causes of morbidity and mortality globally, characterized by complications such as heart failure, atherosclerosis, and coronary artery disease. The vascular endothelium, forming the inner lining of blood vessels, plays a pivotal role in maintaining vascular homeostasis. The dysfunction of endothelial cells contributes significantly to the progression of CVDs, particularly through impaired cellular communication and paracrine signaling with other cell types, such as smooth muscle cells and macrophages. In recent years, co-culture systems have emerged as advanced in vitro models for investigating these interactions and mimicking the pathological environment of CVDs. This review provides an in-depth analysis of co-culture models that explore endothelial cell dysfunction and the role of cellular interactions in the development of vascular diseases. It summarizes recent advancements in multicellular co-culture models, their physiological and therapeutic relevance, and the insights they provide into the molecular mechanisms underlying CVDs. Additionally, we evaluate the advantages and limitations of these models, offering perspectives on how they can be utilized for the development of novel therapeutic strategies and drug testing in cardiovascular research.
引用
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页数:25
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共 178 条
[1]   Early aortic valve inflammation precedes calcification: A longitudinal FDG-PET/CT study [J].
Abdelbaky, Amr ;
Corsini, Erin ;
Figueroa, Amparo L. ;
Subramanian, Sharath ;
Fontanez, Sara ;
Emami, Hamed ;
Hoffmann, Udo ;
Narula, Jagat ;
Tawakol, Ahmed .
ATHEROSCLEROSIS, 2015, 238 (02) :165-172
[2]   Biocompatibility of implants: lymphocyte/macrophage interactions [J].
Anderson, James M. ;
McNally, Amy K. .
SEMINARS IN IMMUNOPATHOLOGY, 2011, 33 (03) :221-233
[3]   Role of Vascular Smooth Muscle Cell Phenotype Switching in Arteriogenesis [J].
Ashraf, Jasni Viralippurath ;
Zen, Ayman Al Haj .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (19)
[4]   Overexpression of endothelial NO synthase induces angiogenesis in a co-culture model [J].
Babaei, S ;
Stewart, DJ .
CARDIOVASCULAR RESEARCH, 2002, 55 (01) :190-200
[5]   Microfluidic Systems for Neural Cell Studies [J].
Babaliari, Eleftheria ;
Ranella, Anthi ;
Stratakis, Emmanuel .
BIOENGINEERING-BASEL, 2023, 10 (08)
[6]   Endothelial cell-to-cell junctions: Molecular organization and role in vascular homeostasis [J].
Bazzoni, G ;
Dejana, E .
PHYSIOLOGICAL REVIEWS, 2004, 84 (03) :869-901
[7]   3D Co-culture of hiPSC-Derived Cardiomyocytes With Cardiac Fibroblasts Improves Tissue-Like Features of Cardiac Spheroids [J].
Beauchamp, Philippe ;
Jackson, Christopher B. ;
Ozhathil, Lijo Cherian ;
Agarkova, Irina ;
Galindo, Cristi L. ;
Sawyer, Douglas B. ;
Suter, Thomas M. ;
Zuppinger, Christian .
FRONTIERS IN MOLECULAR BIOSCIENCES, 2020, 7
[8]   Human primary co-culture angiogenesis assay reveals additive stimulation and different angiogenic properties of VEGF and HGF [J].
Beilmann, M ;
Birk, G ;
Lenter, MC .
CYTOKINE, 2004, 26 (04) :178-185
[9]   The role of pericytes in blood-vessel formation and maintenance [J].
Bergers, G ;
Song, S .
NEURO-ONCOLOGY, 2005, 7 (04) :452-464
[10]   Morphological and Functional Remodeling of Vascular Endothelium in Cardiovascular Diseases [J].
Bkaily, Ghassan ;
Jacques, Danielle .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (03)