Table 1.
Cell Subset | Model System and Methods | Main Finding Regarding Lymphocyte Tissue Residency in the Kidney | Ref. |
---|---|---|---|
NK cells | Mouse, IRI | CD49a+DX5− NK cells are kidney resident | 32 |
Parabiosis, antibody-mediated depletion of circulating NK cells | Kidney-resident NK cells promote IRI | ||
NK cells | Renal biopsies of patients showing different degrees of kidney fibrosis | CD69+ NK cells produce IFN-γ and accumulate in fibrotic kidney tissue | 34 |
CD69 expression by flow cytometry | |||
CD8+ T cells | Mouse, VSV, and listeria infection | Pathogen-specific CD8+ T cells show long-term persistence in the kidney tissue | 8 |
Ag-loaded tetramer staining | |||
CD8+ T cells | Mouse, LCMV infection | Tissue residence of renal LCMV-specific CD8+ T cells | 72 |
Parabiosis, intravascular leukocyte labeling | S1P1 expression prevents renal Trm cell accumulation | ||
Continuous TCR signaling is not required for Trm cell persistence | |||
CD8+ and CD4+ T cells | Mouse, LCMV infection, tumor | i.v. mAb-negative CD69+ CD103± CD4+ and CD8+ Trm cells are found in the kidney tissue | 20 |
Intravascular leukocyte labeling | |||
CD8+ T cells | Mouse, LCMV, and VSV infection | Standard protocols for T cell isolation are inefficient | 17 |
Quantitative immunofluorescence microscopy, intravascular leukocyte labeling | Resident T cells greatly outnumber recirculating cells in nonlymphoid tissues | ||
CD8+ T cells | Mouse, LCMV infection | The transcription factors Blimp1 and Hobit are required for renal Trm development | 78 |
Ag-loaded tetramer staining | |||
CD8+ T cells | Mouse, LCMV infection | TGF-β is required for transendothelial migration of Trm cells into the kidney | 71 |
Intravascular leukocyte labeling |
VSV, varicella zoster virus; Ag, antigen; LCMV, lymphocytic choriomeningitis virus; S1P1, sphingosine phosphate 1 receptor 1, TCR, T cell receptor.