TY - JOUR
T1 - Single-Cell Analysis Reveals That CD47 mRNA Expression Correlates with Immune Cell Activation, Antiviral Isgs, and Cytotoxicity
AU - Cham, Lamin B.
AU - Rosas-Umbert, Miriam
AU - Lin, Lin
AU - Tolstrup, Martin
AU - Søgaard, Ole S.
N1 - Publisher Copyright:
© Copyright by the Author(s). Published by Cell Physiol Biochem Press.
PY - 2024/7/26
Y1 - 2024/7/26
N2 - BACKGROUND/AIMS: Immune cells are reported to upregulate CD47 during infection, however, the role of CD47 in innate and adaptive immune cells remains unclear. METHODS: To bridge this knowledge gap, we analysed our single cell (sc)-RNA dataset along with other publicly available sc-RNA datasets from healthy controls, people with HIV-1 (PWH) and COVID-19 patients. We characterized each immune cell based on low, intermediate, and high expression of CD47 . RESULTS: Our analyses revealed that CD47high pDCs and monocytes exhibited relatively higher expression of IFN-α regulatory genes, antiviral interferon-stimulated genes (ISGs) and MHC-I associated genes compared to CD47inter. and CD47low cells. Furthermore, CD47high NK and CD8+ T cells showed higher expression of antiviral ISGs, as well as genes encoding for cytotoxic markers like granzyme B, perforin, granulysin, interferon gamma and NKG7. Additionally, CD47high CD8+ T cells expressed higher levels of PD-1 and LAG-3 genes. Lastly, we found that CD47high B cells had enriched expression of genes involved in cell activation and humoral responses. CONCLUSION: Overall, our analyses revealed that innate and adaptive immune cells expressing elevated activation and functional gene signatures also express higher CD47 levels.
AB - BACKGROUND/AIMS: Immune cells are reported to upregulate CD47 during infection, however, the role of CD47 in innate and adaptive immune cells remains unclear. METHODS: To bridge this knowledge gap, we analysed our single cell (sc)-RNA dataset along with other publicly available sc-RNA datasets from healthy controls, people with HIV-1 (PWH) and COVID-19 patients. We characterized each immune cell based on low, intermediate, and high expression of CD47 . RESULTS: Our analyses revealed that CD47high pDCs and monocytes exhibited relatively higher expression of IFN-α regulatory genes, antiviral interferon-stimulated genes (ISGs) and MHC-I associated genes compared to CD47inter. and CD47low cells. Furthermore, CD47high NK and CD8+ T cells showed higher expression of antiviral ISGs, as well as genes encoding for cytotoxic markers like granzyme B, perforin, granulysin, interferon gamma and NKG7. Additionally, CD47high CD8+ T cells expressed higher levels of PD-1 and LAG-3 genes. Lastly, we found that CD47high B cells had enriched expression of genes involved in cell activation and humoral responses. CONCLUSION: Overall, our analyses revealed that innate and adaptive immune cells expressing elevated activation and functional gene signatures also express higher CD47 levels.
KW - CD47 ; Immune cells ; Transcriptomic ; Infection ; Antiviral ; Cytotoxic
KW - Infection
KW - Antiviral
KW - Cd47
KW - Cytotoxic
KW - Immune cells
KW - Transcriptomic
UR - http://www.scopus.com/inward/record.url?scp=85200102854&partnerID=8YFLogxK
U2 - 10.33594/000000715
DO - 10.33594/000000715
M3 - Journal article
C2 - 39074350
AN - SCOPUS:85200102854
SN - 1015-8987
VL - 58
SP - 322
EP - 335
JO - Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology
JF - Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology
IS - 4
ER -