SCREATE

Cell state · L2

MAC.kupffer.inflammatory

317 cells in the full atlas (not the displayed sample).

These are the cell-population annotations shown in the SCREATE Cell Browser.

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Marker genes

ABL2, BIRC3, CCL3, CCL4, CSF1, CXCL2, CXCL3, CXCL8, DCSTAMP, EMP1, ICAM1, IER3, MIR155HG, NRIP3, TNFAIP3

Annotation genes

CCL3, CCL4, CXCL8, ICAM1, MIR155HG, TNFAIP3

Annotation rationales

CCL3/4 and CXCL8 recruit monocytes/neutrophils; ICAM1 enhances adhesion; MIR155HG promotes pro-inflammatory polarization; TNFAIP3 is a feedback brake. Annotation genes typify activated Kupffer cells during sepsis/NASH.

Functional implications

Drive leukocyte trafficking to sinusoids, amplify inflammatory circuits, and, via TNFAIP3, prevent runaway hepatocellular damage—key early orchestrators of hepatic innate defense.

Marker and functional descriptions are atlas annotations. Explore gene expression, trait associations and regulatory elements in the interactive browsers; see the browser guide.