1.The function of co-microencapsulated rat islet cell and testicular sertoli cell in vitro
Chinese Journal of Diabetes 2006;14(3):233-234
The pancreatic islet cell and testicular sertoli cells of rat were alone-and co-microencapsulated and cultured for 11 days, then insulin concentration of culture fluid was detected.The results showed that islet function in co-microencapsulated group was better than that in co-culture of microencapsulated islet and microencapsulated testicular sertoli cells and also better than that single microencapsulated islet group (P<0.05).
2.A human circulating immune cell landscape in aging and COVID-19.
Yingfeng ZHENG ; Xiuxing LIU ; Wenqing LE ; Lihui XIE ; He LI ; Wen WEN ; Si WANG ; Shuai MA ; Zhaohao HUANG ; Jinguo YE ; Wen SHI ; Yanxia YE ; Zunpeng LIU ; Moshi SONG ; Weiqi ZHANG ; Jing-Dong J HAN ; Juan Carlos Izpisua BELMONTE ; Chuanle XIAO ; Jing QU ; Hongyang WANG ; Guang-Hui LIU ; Wenru SU
Protein & Cell 2020;11(10):740-770
Age-associated changes in immune cells have been linked to an increased risk for infection. However, a global and detailed characterization of the changes that human circulating immune cells undergo with age is lacking. Here, we combined scRNA-seq, mass cytometry and scATAC-seq to compare immune cell types in peripheral blood collected from young and old subjects and patients with COVID-19. We found that the immune cell landscape was reprogrammed with age and was characterized by T cell polarization from naive and memory cells to effector, cytotoxic, exhausted and regulatory cells, along with increased late natural killer cells, age-associated B cells, inflammatory monocytes and age-associated dendritic cells. In addition, the expression of genes, which were implicated in coronavirus susceptibility, was upregulated in a cell subtype-specific manner with age. Notably, COVID-19 promoted age-induced immune cell polarization and gene expression related to inflammation and cellular senescence. Therefore, these findings suggest that a dysregulated immune system and increased gene expression associated with SARS-CoV-2 susceptibility may at least partially account for COVID-19 vulnerability in the elderly.
Adult
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Aged
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Aged, 80 and over
;
Aging
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genetics
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immunology
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Betacoronavirus
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CD4-Positive T-Lymphocytes
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metabolism
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Cell Lineage
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Chromatin Assembly and Disassembly
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Coronavirus Infections
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immunology
;
Cytokine Release Syndrome
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etiology
;
immunology
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Cytokines
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biosynthesis
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genetics
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Disease Susceptibility
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Flow Cytometry
;
methods
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Gene Expression Profiling
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Gene Expression Regulation, Developmental
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Gene Rearrangement
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Humans
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Immune System
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cytology
;
growth & development
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immunology
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Immunocompetence
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genetics
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Inflammation
;
genetics
;
immunology
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Mass Spectrometry
;
methods
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Middle Aged
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Pandemics
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Pneumonia, Viral
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immunology
;
Sequence Analysis, RNA
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Single-Cell Analysis
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Transcriptome
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Young Adult