Pseudolycorine chloride ameliorates Th17 cell-mediated central nervous system autoimmunity by restraining myeloid-derived suppressor cell expansion

Pharm Biol. 2022 Dec;60(1):899-908. doi: 10.1080/13880209.2022.2063344.

Abstract

Context: The alkaloids of Narcissus tazetta L. var. Chinensis Roem (Amaryllidaceae) have antitumor and antiviral activities. However, the immunopharmacological effects of one of its constituents, pseudolycorine chloride (PLY), have not been reported yet.

Objective: We evaluated the effect of PLY on myeloid-derived suppressor cells (MDSCs) expansion and differentiation into monocyte-like MDSCs (M-MDSCs) and examined whether PLY alleviates Th17 cell-mediated experimental autoimmune encephalomyelitis (EAE), a murine model of multiple sclerosis (MS).

Materials and methods: In vitro, MDSCs were treated with PLY (0.67, 2 and 6 μM) or solcitinib (10 μM, positive control) for 48 or 96 h, and their proliferation, expansion, and differentiation into M-MDSCs were examined by flow cytometry. Myelin oligodendrocyte glycoprotein (MOG35-55) was used to induce EAE in female C57BL/6 mice, and the mice were treated with 40 mg/kg/d PLY or 1 mg/kg/d FK-506 (tacrolimus, positive control) for 21 days. Inflammatory infiltration, spinal cord demyelination, and MDSCs and Th17 cells infiltration into the spinal cord were examined using haematoxylin and eosin staining, Luxol fast blue staining, and immunofluorescence, respectively.

Results: In vitro, PLY (IC50/24 h = 6.18 μM) significantly inhibited IL-6 and GM-CSF-induced MDSCs proliferation, expansion and differentiation into M-MDSCs at all concentrations used. However, these concentrations did not show cytotoxicity. In mice, PLY (40 mg/kg) treatment alleviated EAE and inhibited inflammatory infiltration, demyelination, and MDSCs and Th17 cells infiltration into the spinal cord.

Discussion and conclusions: PLY may be an excellent candidate for the treatment of MS and other autoimmune diseases.

Keywords: IL-17A; M-MDSCs; MDSCs; experimental autoimmune encephalomyelitis/multiple sclerosis; immunosuppression.

MeSH terms

  • Amaryllidaceae Alkaloids
  • Animals
  • Autoimmunity
  • Cell Proliferation
  • Central Nervous System / pathology
  • Chlorides / pharmacology
  • Cytokines
  • Encephalomyelitis, Autoimmune, Experimental* / drug therapy
  • Encephalomyelitis, Autoimmune, Experimental* / pathology
  • Female
  • Mice
  • Mice, Inbred C57BL
  • Myeloid-Derived Suppressor Cells* / pathology
  • Phenanthridines
  • Th17 Cells

Substances

  • Amaryllidaceae Alkaloids
  • Chlorides
  • Cytokines
  • Phenanthridines
  • pseudolycorine

Grants and funding

This work was supported by the National Natural Science Foundation of China (No. 81871300, No. 31870341), Department of Science and Technology of Sichuan Province (CN) (No. 2021YJ0126), Chengdu Science and Technology Bureau (No. 2021-YF05-00975-SN), the Research Fund of Chengdu Medical College (No. CYTD18-01), Graduate Innovation Fund (No. YCX2020-02), and Disciplinary Construction Innovation Team Foundation of Chengdu Medical College (No. CMC-XK-2103).