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Circulating ILC precursors expressing CD62L exhibit a type 2 signature distinctly decreased in psoriatic patients.

ABSTRACT: Human CD117⁺ CRTH2^neg innate lymphoid cells (ILC) comprise multipotent precursors (ILCp), which are able to differentiate into subtypes in response to different signals received in peripheral tissues. NKp46⁺ ILCp have been reported to associate with ILC3 whereas KLRG1⁺ ILCp with ILC2, although the latter can also generate other ILC subsets, thus, maintaining a substantial plasticity. We here showed that CD62L is expressed by ILCp exclusively within KLRG1⁺ population and its expression marks a loss of their broad differentiation potential. Analysis of cytokine production and relevant markers demonstrated that CD62L⁺ ILCp mainly differentiate into ILC2 whereas CD62L^neg counterpart can also differentiate into other ILC subsets depending on the signals they receive. Remarkably, in peripheral blood of psoriatic patients, where ILC3 are usually enriched, CD62L⁺ ILC were drastically reduced, whereas CD62L^neg ILC2 upregulated both RORγt and NKp46, thus, suggesting an ongoing conversion to ILC3. Therefore, CD62L now emerges as a potential marker to identify a skewing toward type 2 among ILCp.

SUBMITTER: Campana S

PROVIDER: S-EPMC8360187 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Striatal neurons expressing full-length mutant huntingtin exhibit decreased N-cadherin and altered neuritogenesis.

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2017-03-19 | GSE90640 | GEO

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Project description: Not available

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