Expression of Endogenous Angiotensin-Converting Enzyme 2 in Human Induced Pluripotent Stem Cell-Derived Retinal Organoids

Autor: Chih Chien Hsu, Shih Jie Chou, Shih Hwa Chiou, Tai Chi Lin, Yi Ping Yang, Yueh Chien, Chian Shiu Chien, De Kuang Hwang, Ying Chun Jheng, Henkie Isahwan Ahmad Mulyadi Lai, Ping Hsing Tsai, Yu Bai Chou, Shih-Jen Chen, Mong Lien Wang
Rok vydání: 2020
Předmět:
0301 basic medicine
induced pluripotent stem cells
Cell Culture Techniques
Gene Expression
ACE2
Biology
spike protein
TMPRSS2
Catalysis
Retina
Article
Green fluorescent protein
Cell Line
Inorganic Chemistry
lcsh:Chemistry
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Organoid
medicine
Humans
Physical and Theoretical Chemistry
Receptor
Induced pluripotent stem cell
Molecular Biology
lcsh:QH301-705.5
Spectroscopy
SARS-CoV-2
Organic Chemistry
fungi
Serine Endopeptidases
COVID-19
SARS-CoV-2 pseudovirus
Retinal
General Medicine
Virus Internalization
Computer Science Applications
Cell biology
Organoids
030104 developmental biology
medicine.anatomical_structure
chemistry
lcsh:Biology (General)
lcsh:QD1-999
Cell culture
Angiotensin-Converting Enzyme 2
030217 neurology & neurosurgery
Zdroj: International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 1320, p 1320 (2021)
Volume 22
Issue 3
ISSN: 1422-0067
Popis: Angiotensin-converting enzyme 2 (ACE2) was identified as the main host cell receptor for the entry of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and its subsequent infection. In some coronavirus disease 2019 (COVID-19) patients, it has been reported that the nervous tissues and the eyes were also affected. However, evidence supporting that the retina is a target tissue for SARS-CoV-2 infection is still lacking. This present study aimed to investigate whether ACE2 expression plays a role in human retinal neurons during SARS-CoV-2 infection. Human induced pluripotent stem cell (hiPSC)-derived retinal organoids and monolayer cultures derived from dissociated retinal organoids were generated. To validate the potential entry of SARS-CoV-2 infection in the retina, we showed that hiPSC-derived retinal organoids and monolayer cultures endogenously express ACE2 and transmembrane serine protease 2 (TMPRSS2) on the mRNA level. Immunofluorescence staining confirmed the protein expression of ACE2 and TMPRSS2 in retinal organoids and monolayer cultures. Furthermore, using the SARS-CoV-2 pseudovirus spike protein with GFP expression system, we found that retinal organoids and monolayer cultures can potentially be infected by the SARS-CoV-2 pseudovirus. Collectively, our findings highlighted the potential of iPSC-derived retinal organoids as the models for ACE2 receptor-based SARS-CoV-2 infection.
Databáze: OpenAIRE