Hsp90/Sec22b promotes unconventional secretion of mature-IL-1β through an autophagosomal carrier in porcine alveolar macrophages during Mycoplasma hyopneumoniae infection

• Published in: Molecular immunology Vol. 101; pp. 130 - 139
• Main Authors: Zhang, Zhenzhen, Wei, Yanna, Liu, Beibei, Wu, Yuzi, Wang, Haiyan, Xie, Xing, Feng, Zhixin, Shao, Guoqing, Xiong, Qiyan
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.09.2018
• Subjects: Autophagosome; IL-1β; Mycoplasma hyopneumoniae; Unconventional secretion; Unconventional secretion; Mycoplasma hyopneumoniae; IL-1β; Autophagosome
• ISSN: 0161-5890; 1872-9142
• DOI: 10.1016/j.molimm.2018.06.265

•M. hyopneumoniae infection increased the secretion of mature IL-1β.•M. hyopneumoniae infection promoted the generation of autophagosomes.•Hsp90 was required for the entry of mature IL-1β into autophagosome.•Sec22b controlled the fusion of IL-1β-containing autophagosome and plasma membranes. Interleukin-1β (IL-1β) is a critical inflammatory regulator in response to Mycoplasma hyopneumoniae infection. However, the mechanism involved in the secretion of IL-1β during Mycoplasma hyopneumoniae infection is unclear. In this study, we demonstrated that Mycoplasma hyopneumoniae infection increased the secretion of mature-IL-1β (m-IL-1β), but not pro-IL-1β, in porcine alveolar macrophages. Moreover, Mycoplasma hyopneumoniae infection promoted the generation of autophagosomes, which attributed to the unconventional secretion of m-IL-1β. Further results revealed that Hsp90 was required for the entry of m-IL-1β into autophagosomes during Mycoplasma hyopneumoniae infection. The fusion of m-IL-1β-containing autophagosome and plasma membranes was regulated by Sec22b and independent of lysosomal dysfunction. In conclusion, we provide evidence that Hsp90/Sec22b promotes the unconventional secretion of IL-1β through an autophagosomal carrier during Mycoplasma hyopneumoniae infection. The elucidation of the molecular and cellular machinery in Mycoplasma hyopneumoniae infected mammalian cells in this study suggests avenues for further study and applications and paves the way for novel therapeutic strategies to prevent tissue damage in mycoplasma-associated diseases.