“…In the stroke model dataset produced by Shi et al (2021) , some of the clusters did not solely and selectively express their markers [ CD3 antigen, epsilon polypeptide ( Cd3e ), T cell marker ( Shi et al, 2021 ); membrane-spanning 4-domains, subfamily A, member 7 ( Ms4a7 ), macrophage marker ( Milich et al, 2021 ); natural killer cell group 7 sequence ( Nkg7 ), natural killer (NK) cell marker ( Wu et al, 2021 ), Fc receptor, IgE, high affinity I, alpha polypeptide ( Fcer1a ), dendritic cell marker ( Wu et al, 2021 ); solute carrier family 4, sodium bicarbonate cotransporter, member 5 ( Slc4a5 ), choroid plexus epithelial cell marker ( Shi et al, 2021 ); collagen, type I, alpha 1 ( Col1a1 ), fibroblast marker ( Milich et al, 2021 ); Cx3cr1 , microglial marker; ( Supplementary Figure 3B )]. However, the other cells, including astrocytes that are the focus of this study, selectively expressed their markers [ Lactotransferrin ( Ltf ), neutrophil (granulocyte) marker ( Milich et al, 2021 ); RNA binding protein, fox-1 homolog 3 ( Rbfox3 ), neuronal marker ( Ikeda-Yorifuji et al, 2022 ); platelet/endothelial cell adhesion molecule 1 ( Pecam1 ), endothelial cell marker ( Ikeda-Yorifuji et al, 2022 ); Slc7a1 ( Ikeda-Yorifuji et al, 2022 ) and Aldh1l1 , astrocyte markers; myelin oligodendrocyte glycoprotein ( Mog ), oligodendrocyte marker; Ikeda-Yorifuji et al, 2022 ; Supplementary Figure 3B ]. In a systemic inflammation model produced by intraperitoneal injection of lipopolysaccharide (LPS) by Hasel et al (2021) , all clusters (oligodendrocytes, microglia, neurons, endothelial cells, and astrocytes) selectively expressed these markers ( Supplementary Figure 3C ).…”