British journal of pharmacology · 2026
Leflunomide-inhibited STAT1 activity ameliorates intramuscular M1 macrophage infiltration and promotes muscle regeneration in Duchenne muscular dystrophy.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Hu Wanting, Tong Haowei, Zhu Maolin, Wang Huna, Huang Xiaofei, Fan Shusheng, Guo Guangyao, Ismail Mohammed, Zhao Lei, Li Xihua, Zhang Luyong, Yu Qinwei, Jiang Zhenzhou
Аннотация
BACKGROUND AND PURPOSE: Duchenne muscular dystrophy (DMD) is an X-linked recessive disorder caused by dystrophin gene mutations. This study investigated the therapeutic effects of leflunomide, a STAT1 inhibitor on dystrophic muscles.
EXPERIMENTAL DESIGN: The characterization of M1 macrophage polarization and the level of STAT1/p-STAT1 were measured in DMD patients. Lipopolysaccharide (LPS)/IFN-γ and RO8191 were selected to stimulate STAT1 for evaluating the inhibitory effect of A771726 on M1 polarization and STAT1. Conditionally cocultured M1 RAW264.7 cells and differentiated C2C12 myoblasts were used to explore the differentiation of A771726 to myopathy in inflammatory environments. After 4-week treatment with leflunomide, the protein levels of STAT1 and p-STAT1 were evaluated in mdx mice. CD86 and CD68 were selected for evaluating inflammation event. The proinflammatory cytokines were measured by RT-PCR and ELISA. Muscle function and myofibre damage were examined by behavioural experiments and serum CK and LDH level, respectively. The muscle regeneration event was demonstrated by myosin heavy chain, myogenic differentiation (MyOD) protein levels and eMyHC immunofluorescence.
KEY RESULTS: STAT1 was remarkably upregulated in mdx mice and DMD patients compared with control groups. A771726 restrained LPS/IFN-γ-induced M1 macrophage polarization via inhibiting p-STAT1 and STAT1. Specific activation of STAT1 by RO8191 promoted macrophage polarize towards M1 type, which was partially counteracted by A771726. Leflunomide-inhibited inflammation infiltration mediated by M1 macrophage and exerted promising therapeutic effect on muscle repair in mdx mice.
CONCLUSIONS AND IMPLICATIONS: Leflunomide relieved M1 macrophage infiltration and improved muscle regeneration by downregulating STAT1 and p-STAT1. STAT1 may merge as a promising target for the therapy of DMD.
EXPERIMENTAL DESIGN: The characterization of M1 macrophage polarization and the level of STAT1/p-STAT1 were measured in DMD patients. Lipopolysaccharide (LPS)/IFN-γ and RO8191 were selected to stimulate STAT1 for evaluating the inhibitory effect of A771726 on M1 polarization and STAT1. Conditionally cocultured M1 RAW264.7 cells and differentiated C2C12 myoblasts were used to explore the differentiation of A771726 to myopathy in inflammatory environments. After 4-week treatment with leflunomide, the protein levels of STAT1 and p-STAT1 were evaluated in mdx mice. CD86 and CD68 were selected for evaluating inflammation event. The proinflammatory cytokines were measured by RT-PCR and ELISA. Muscle function and myofibre damage were examined by behavioural experiments and serum CK and LDH level, respectively. The muscle regeneration event was demonstrated by myosin heavy chain, myogenic differentiation (MyOD) protein levels and eMyHC immunofluorescence.
KEY RESULTS: STAT1 was remarkably upregulated in mdx mice and DMD patients compared with control groups. A771726 restrained LPS/IFN-γ-induced M1 macrophage polarization via inhibiting p-STAT1 and STAT1. Specific activation of STAT1 by RO8191 promoted macrophage polarize towards M1 type, which was partially counteracted by A771726. Leflunomide-inhibited inflammation infiltration mediated by M1 macrophage and exerted promising therapeutic effect on muscle repair in mdx mice.
CONCLUSIONS AND IMPLICATIONS: Leflunomide relieved M1 macrophage infiltration and improved muscle regeneration by downregulating STAT1 and p-STAT1. STAT1 may merge as a promising target for the therapy of DMD.