Larijani Bagher, Foroughi-Heravani Najmeh, Abedi Mina, Tayanloo-Beik Akram, Rezaei-Tavirani Mostafa, Adibi Hossein, Arjmand Babak
Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical sciences, Tehran, Iran.
Cell Therapy and Regenerative Medicine Research Center, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
Front Cell Dev Biol. 2021 Oct 25;9:683619. doi: 10.3389/fcell.2021.683619. eCollection 2021.
Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) has caused a pandemic since December 2019 that originated in Wuhan, China. Soon after that, the world health organization declared Coronavirus disease-2019 a global health concern. SARS-CoV-2 is responsible for a lethal respiratory infection as well as the involvement of other organs due to its large tropism spectrum such as neurologic, cardiovascular, endocrine, gastrointestinal, and renal systems. Since the behavior of the virus is not fully understood, a new manifestation of the infection is revealed every day. In order to be able to design more efficient drugs and vaccines to treat the infection, finding out the exact mechanism of pathogenicity would be necessary. Although there have been some big steps toward understanding the relevant process, there are still some deficiencies in this field. Accordingly, regenerative medicine (RM), can offer promising opportunities in discovering the exact mechanisms and specific treatments. For instance, since it is not always possible to catch the pathophysiology mechanisms in human beings, several modeling methods have been introduced in this field that can be studied in three main groups: stem cell-based models, organoids, and animal models. Regarding stem cell-based models, induced pluripotent stem cells are the major study subjects, which are generated by reprogramming the somatic stem cells and then directing them into different adult cell populations to study their behavior toward the infection. In organoid models, different cell lines can be guided to produce a 3D structure including liver, heart, and brain-like platforms. Among animal models, mice are the most common species in this field. However, in order for mice models to be permissive to the virus, angiotensin-converting enzyme 2 receptors, the main receptor involved in the pathogenicity of the virus, should be introduced to the host cells through different methods. Here, the current known mechanism of SARS-CoV-2 infection, different suggested models, the specific response toward different manipulation as well as challenges and shortcomings in each case have been reviewed. Finally, we have tried to provide a quick summary of the present available RM-based models for SARS-CoV-2 infection, as an essential part of developing drugs, for future therapeutic goals.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)自2019年12月在中国武汉引发疫情以来,已在全球范围内大流行。此后不久,世界卫生组织宣布2019冠状病毒病为全球卫生关注重点。SARS-CoV-2可导致致命的呼吸道感染,还因其广泛的嗜性,累及神经系统、心血管系统、内分泌系统、胃肠道和肾脏系统等其他器官。由于对该病毒的行为尚未完全了解,每天都会发现感染的新表现。为了能够设计出更有效的药物和疫苗来治疗感染,有必要找出确切的致病机制。尽管在理解相关过程方面已经取得了一些重大进展,但该领域仍存在一些不足。因此,再生医学(RM)在发现确切机制和特定治疗方法方面可以提供有前景的机会。例如,由于在人类中并不总是能够捕捉到病理生理机制,该领域已经引入了几种建模方法,主要可分为三大类:基于干细胞的模型、类器官和动物模型。在基于干细胞的模型中,诱导多能干细胞是主要的研究对象,通过对体细胞进行重编程,然后将其定向分化为不同的成体细胞群体,以研究它们对感染的反应。在类器官模型中,可以引导不同的细胞系形成三维结构,包括肝脏、心脏和大脑样平台。在动物模型中,小鼠是该领域最常用的物种。然而,为了使小鼠模型能够感染该病毒,需要通过不同方法将病毒致病性的主要受体血管紧张素转换酶2受体引入宿主细胞。在此,本文综述了SARS-CoV-2感染的当前已知机制、不同的建议模型、对不同操作的特异性反应以及每种情况下的挑战和不足。最后,我们试图快速总结目前可用的基于再生医学的SARS-CoV-2感染模型,作为开发药物的重要组成部分,以实现未来的治疗目标。