A new species of Strotarchus Simon, 1888 from Mexico and description of the male of the type species S. nebulosus Simon, 1888 (Araneae: Cheiracanthiidae)

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  A new species of Strotarchus Simon, 1888 from Mexico and description of the male of the type species S. nebulosus Simon, 1888 (Araneae: Cheiracanthiidae) Abstract A new sac spider of the genus Strotarchus Simon, 1888, S. adrianae spec. nov., is described based on specimens of both sexes collected from Jalisco, Mexico. In addition, the previously unknown male of Strotarchus nebulosus Simon, 1888 is described for the first time. Orozco-Gil, M., Jiménez, M.-L. & Chamé-Vázquez, D. (2026) A new species of Strotarchus Simon, 1888 from Mexico and description of the male of the type species S. nebulosus Simon, 1888 (Araneae: Cheiracanthiidae). Zootaxa, 5821 (2), 263–273. https://doi.org/10.11646/zootaxa.5821.2.7

F1 fraction isolated from Mesobuthus eupeus scorpion venom induces macrophage polarization toward M1 phenotype and exerts anti-tumoral effects on the CT26 tumor cell line

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F1 fraction isolated from Mesobuthus eupeus scorpion venom induces macrophage polarization toward M1 phenotype and exerts anti-tumoral effects on the CT26 tumor cell line

Abstract

Scorpion venoms identified as agents with anti-tumor and anti-angiogenic features. Tumor microenvironment (TME) plays a pivotal role in the process of tumorigenesis, tumor development, and polarization of M2 phenotype tumor associated macrophages (TAMs). M2 polarized cells are associated with tumor growth, invasion, and metastasis. The fractionation process was performed by gel filtration chromatography on a Sephadex G50 column. To elucidate whether scorpion venom can alter macrophage polarization, we treated interleukin (IL)-4-polarized M2 cells with isolated fractions from Mesobuthus eupeus. Next, we evaluated the cytokine production and specific markers expression for M2 and M1 phenotype using enzyme linked immunosorbent assay (ELISA) and real-time polymerase chain reaction (PCR), respectively. The phagocytic capacity of macrophages was also assessed. In addition, the migration assay and MTT analysis were performed to investigate the effects of reprogrammed macrophages on the CT-26 colon cancer cells. The results indicated that F1 fraction of venom significantly upregulated the levels and expression of M1-associated cytokines and markers, including tumor necrosis factor-alpha (TNF-α) (p < 0.001), IL-1 (p < 0.01), interferon regulatory factor 5 (IRF5) (p < 0.0001), induced nitric oxide synthase (iNOS) (p < 0.0001), and CD86 (p < 0.0001), and downregulated M2-related markers, including transforming growth factor-beta (TGF-β) (p < 0.05), IL-10 (p < 0.05), Fizz1 (p < 0.0001), arginase-1 (Arg-1) (p < 0.0001), and CD206 (p < 0.001). The macrophage phagocytic capacity was enhanced after treatment with F1 fraction (p < 0.01). Moreover, incubation of CT-26 cell line with conditioned media of F1-treated macrophages suppressed migration (p < 0.0001) and proliferation (p < 0.01) of tumor cells. In conclusion, our findings demonstrated the potential of Mesobuthus eupeus venom in M2-to-M1 macrophage polarization as a promising therapeutic approach against proliferation and metastasis of colon cancer cells.


Sadeghi, M., Amari, A., Asadirad, A., Nemati, M., & Khodadadi, A. (2024). F1 fraction isolated from Mesobuthus eupeus scorpion venom induces macrophage polarization toward M1 phenotype and exerts anti-tumoral effects on the CT26 tumor cell line. International Immunopharmacology, 132, 111960. https://doi.org/10.1016/j.intimp.2024.111960