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Division of Immunology, Boston Childrens Hospital, Boston, Massachusetts, USADepartment of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA
Division of Immunology, Boston Childrens Hospital, Boston, Massachusetts, USADepartment of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA
Monitoring cellular movement with photoconvertible fluorescent protein and single-cell RNA sequencing reveals cutaneous group 2 inate lymphoid cell subtypes, circulating ILC2 and skin-resident ILC2.
show that type 2 innate lymphoid cells (ILC2s) in the skin of mice with IL-33 overexpression in keratinocytes are heterogeneous and consist of two distinct populations: skin-resident ILC2s and circulating ILC2s. They show that the circulating subset of skin ILC2s migrates to draining lymph nodes during hapten-induced cutaneous inflammation to potentially enhance the adaptive immune response.
Atopic dermatitis (AD) is the most common skin inflammatory disease and affects 10–20% of infants in the United States and worldwide (
). AD skin lesions demonstrate increased expression of type-2‒promoting epithelial cytokines IL-33, TSLP, and IL-25 and increased numbers of type 2 innate lymphoid cells (ILC2s) that express high levels of receptors for these cytokines (
). ILC2s lack distinct lineage markers as well as antigen-specific surface receptors and are enriched at the interfaces between the body and the environment (
Monitoring cellular movement with photoconvertible fluorescent protein and single-cell RNA sequencing reveals cutaneous group 2 inate lymphoid cell subtypes, circulating ILC2 and skin-resident ILC2.
identify two distinct populations of cutaneous ILC2s by single-cell RNA-sequencing (RNAseq) analysis of skin from hK14-mIl33‒transgenic mice that overexpress IL-33 selectively in keratinocytes (KCs). Analysis of sorted ILC2s from the skin and skin-draining lymph nodes (LNs) of these mice reveals two distinct populations of ILC2s with different gene expression profiles: an ILC2 population restricted to the skin and an ILC2 population present in both the skin and the skin-draining LNs. Skin-resident ILC2s express CD103 and high levels of IL2Rα (CD25) and type 2 cytokines IL-5 and IL-13, whereas circulating ILC2s express KLRG1 and major histocompatibility complex (MHC) class II molecules. These differences were confirmed by flow cytometry and immunofluorescence. Moreover,
Monitoring cellular movement with photoconvertible fluorescent protein and single-cell RNA sequencing reveals cutaneous group 2 inate lymphoid cell subtypes, circulating ILC2 and skin-resident ILC2.
elegantly show that circulating ILC2s present in the skin but not skin-resident ILC2s migrate from the skin to draining LNs using double transgenic mice that express IL-33 in KCs as well as the photoconvertible fluorescence protein KikGR. Violet light irradiation of the skin of KikGR-transgenic mice changes the fluorescence spectrum of KikGR in cutaneous cells from green to red, allowing to track resident skin cells at the moment of irradiation. Induction of skin inflammation in oxazolone-sensitized double transgenic mice after cutaneous hapten challenge enhanced the migration of circulating ILC2s from the skin to the draining LNs (Figure 1). Thus, cutaneous ILC2s have the potential to activate the two arms of the immune response, with skin-resident ILC2s being responsible for the activation of local innate immunity, whereas circulating ILC2s present in the skin being able to potentially drive adaptive immunity by their ability to present antigen‒MHC complexes and to secrete cytokines.
Figure 1Schematic summary of the heterogeneity of skin ILC2s in hK14-mIl33‒transgenic mice. Nakatani-Kusakabe et al. (2021) identify two distinct populations of ILC2s in the skin of mice with keratinocyte-specific expression. Skin-resident ILC2s express CD103, high levels of CD25, and type 2 cytokines, whereas circulating ILC2s express KLRG1 and MHC class II molecules and have the capacity to migrate to draining LNs. Migration of circulating ILC2s from the skin to LNs is enhanced during oxazolone-induced contact dermatitis, raising the possibility that circulating ILC2s modulate the adaptive immune response to cutaneously encountered antigen in the skin-draining LNs. ILC2, type 2 innate lymphoid cell; LN, lymph node; MHC, major histocompatibility complex.
There are some limitations to the conclusions of this elegant study. The use of skin-specific Il33-transgenic mice and the sorting strategy to isolate ILC2s for subsequent single-cell RNAseq analysis could bias the nature of ILC2s analyzed. Transgenic overexpression of Il33 in the skin together with the elevated expression of IL-33 receptor that it causes in skin ILC2s and possibly other cells, for example, mast cells, regulatory T cells (Tregs), and basophils, may influence directly or indirectly the ILC2 recruitment to the skin as well as their phenotype and function.
Activation of ILC2s during calcipotriol (MC903)-induced dermatitis, which is independent of adaptive immunity, highly depends on TSLP in the B6 background, whereas it depends on IL-25 in the BALB/c background (
). We recently showed that the activation of ILC2s by IL-25 is essential for their IL-13 production in mouse skin epicutaneously sensitized with an allergen (
Monitoring cellular movement with photoconvertible fluorescent protein and single-cell RNA sequencing reveals cutaneous group 2 inate lymphoid cell subtypes, circulating ILC2 and skin-resident ILC2.
is whether the two distinct populations of cutaneous ILC2s exist in normal mouse skin or in other mouse models of skin inflammation and importantly in normal or inflamed human skin. Single-cell RNAseq analysis of healthy and AD lesional skin shows that skin ILCs are a heterogeneous population, including ILC1s, ILC2s, ILC3s, and ILC precursors, with ILC2s being predominant (
). Furthermore, ILC2s in normal human skin were found to be a homogenous population that expresses type 2 cytokines IL-13 and IL-4 and the transcription factor GATA3, whereas ILC2s present in AD lesional skin were found to be heterogeneous and expressed type 2 as well as type 17 cytokines and the transcription factors that drive these cytokines, including GATA3, AHR, and RORC (
). These results highlight the important role of the microenvironment in ILC2 activation and plasticity in the skin.
ILC2s control the adaptive immune response locally promoting the activation of dendritic cells, suppressing Treg functions, interacting with CD4+ T cells, and inducing chemoattraction of T helper type 2 cells (
Monitoring cellular movement with photoconvertible fluorescent protein and single-cell RNA sequencing reveals cutaneous group 2 inate lymphoid cell subtypes, circulating ILC2 and skin-resident ILC2.
raises the exciting possibility that this subpopulation of skin ILC2s modulates the adaptive immune response to cutaneously encountered antigen in skin-draining LNs.
Monitoring cellular movement with photoconvertible fluorescent protein and single-cell RNA sequencing reveals cutaneous group 2 inate lymphoid cell subtypes, circulating ILC2 and skin-resident ILC2.
We previously generated a transgenic mouse line expressing skin-specific IL-33 (IL33tg mice) and showed that IL-33 elicits group 2 innate lymphoid cell (ILC2)–dependent atopic dermatitis–like skin inflammation. ILC2s are believed to be tissue-resident cells under steady-state conditions, but the dynamics of ILC2 migration are not fully understood. We sorted ILC2s from the skin and draining lymph nodes of IL33tg mice and analyzed their transcriptomes using the single-cell RNA sequencing technique, which revealed that the skin ILC2s had split into two clusters: circulating ILC2 and skin-resident ILC2.
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