Mesenchymal stromal/stem cells from perinatal sources: biological facts, molecular biomarkers, and therapeutic promises

被引:0
作者
Mohammed Z. Allouh [1 ]
Syed Faizan Ali Rizvi [2 ]
Ali Alamri [2 ]
Yusuf Jimoh [3 ]
Salma Aouda [2 ]
Zakaria H. Ouda [3 ]
Mohammad I. K. Hamad [2 ]
Mick Perez-Cruet [3 ]
G. Rasul Chaudhry [4 ]
机构
[1] Department of Anatomy, College of Medicine and Health Sciences, United Arab Emirates University, P. O. Box: 15551, Al Ain
[2] OU-WB Institute for Stem Cell and Regenerative Medicine, Oakland University, Rochester, 48309, MI
[3] Department of Biological Sciences, Oakland University, Rochester, 48309, MI
[4] College of Medicine and Health Sciences, Khalifa University, Abu Dhabi
[5] Department of Neurosurgery, Corewell Health, Royal Oak, MI
基金
美国国家卫生研究院;
关键词
Degenerative disease; Multipotent; Progenitor cells; Regenerative medicine; Stem cells;
D O I
10.1186/s13287-025-04254-0
中图分类号
学科分类号
摘要
The use of mesenchymal stem cells (MSCs) from perinatal tissue sources has gained attention due to their availability and lack of significant ethical or moral concerns. These cells have a higher proliferative capability than adult MSCs and less immunogenic or tumorigenesis risk than fetal and embryonic stem cells. Additionally, they do not require invasive isolation methods like fetal and adult MSCs. We reviewed the main biological and therapeutic aspects of perinatal MSCs in a three-part article. In the first part, we revised the main biological features and characteristics of MSCs and the advantages of perinatal MSCs over other types of SCs. In the second part, we provided a detailed molecular background for the main biomarkers that can be used to identify MSCs. In the final part, we appraised the therapeutic application of perinatal MSCs in four major degenerative disorders: degenerative disc disease, retinal degenerative diseases, ischemic heart disease, and neurodegenerative diseases. In conclusion, there is no single specific molecular marker to identify MSCs. We recommend using at least two positive markers of stemness (CD29, CD73, CD90, or CD105) and two negative markers (CD34, CD45, or CD14) to exclude the hematopoietic origin. Moreover, utilizing perinatal MSCs for managing degenerative diseases presents a promising therapeutic approach. This review emphasizes the significance of employing more specialized progenitor cells that originated from the perinatal MSCs. The review provides scientific evidence from the literature that applying these progenitor cells in therapeutic procedures provides a greater regenerative capacity than the original primitive MSCs. Finally, this review provides a valuable reference for researchers exploring perinatal MSCs and their therapeutic applications. © The Author(s) 2025.
引用
收藏
相关论文
共 160 条
[91]  
Zhao T., Liang Q., Meng X., Duan P., Wang F., Li S., Et al., Intravenous infusion of umbilical cord mesenchymal stem cells maintains and partially improves visual function in patients with advanced retinitis pigmentosa, Stem Cells Dev, 29, pp. 1029-1037, (2020)
[92]  
Huang C., Zhang J., Ao M., Li Y., Zhang C., Xu Y., Et al., Combination of retinal pigment epithelium cell-conditioned medium and photoreceptor outer segments stimulate mesenchymal stem cell differentiation toward a functional retinal pigment epithelium cell phenotype, J Cell Biochem, 113, pp. 590-598, (2012)
[93]  
Adak S., Magdalene D., Deshmukh S., Das D., Jaganathan B.G., A review on mesenchymal stem cells for treatment of retinal diseases, Stem Cell Rev Rep, 17, pp. 1154-1173, (2021)
[94]  
Safwat A., Sabry D., Ragiae A., Amer E., Mahmoud R.H., Shamardan R.M., Adipose mesenchymal stem cells-derived exosomes attenuate retina degeneration of streptozotocin-induced diabetes in rabbits, J Circ Biomark, 7, (2018)
[95]  
Yu B., Shao H., Su C., Jiang Y., Chen X., Bai L., Et al., Exosomes derived from MSCs ameliorate retinal laser injury partially by Inhibition of MCP-1, Sci Rep, 6, (2016)
[96]  
Mathew B., Ravindran S., Liu X., Torres L., Chennakesavalu M., Huang C.-C., Et al., Mesenchymal stem cell-derived extracellular vesicles and retinal ischemia-reperfusion, Biomaterials, 197, pp. 146-160, (2019)
[97]  
Wang Y., Tang Z., Gu P., Stem/progenitor cell-based transplantation for retinal degeneration: a review of clinical trials, Cell Death Dis, 11, (2020)
[98]  
Bhattacharya S., Gangaraju R., Chaum E., Recent advances in retinal stem cell therapy, Curr Mol Biol Rep, 3, pp. 172-182, (2017)
[99]  
Cotrim C.C., Toscano L., Messias A., Jorge R., Siqueira R.C., Intravitreal use of bone marrow mononuclear fraction containing CD34 + stem cells in patients with atrophic age-related macular degeneration, Clin Ophthalmol Auckl NZ, 11, pp. 931-938, (2017)
[100]  
Chen Y., Shen H., Ding Y., Yu Y., Shao L., Shen Z., The application of umbilical cord-derived MSCs in cardiovascular diseases, J Cell Mol Med, 25, pp. 8103-8114, (2021)