Botulinum toxin type A interrupts autophagic flux of submandibular gland

Biosci Rep. 2019 Jul 23;39(7):BSR20190035. doi: 10.1042/BSR20190035. Print 2019 Jul 31.

Abstract

Botulinum toxin type A (BTXA) is a neurotoxic protein produced by Clostridium botulinum Our previous studies demonstrated that BTXA inhibits the secretory function of submandibular gland (SMG) and changes its structure. Several studies reported that SMG damage and repair often occur with autophagy in the rat. However, no studies reported whether secretory inhibition and structural changes of SMG after BTXA injection is related with autophagy. The present study was carried out to explore the association between BTXA injection and autophagy in rat SMG. Western blotting and immunofluorescence were used to detect the expression and distribution of light chain 3 (LC3) in rat SMG. MTS was used to detect the toxicity of BTXA on rat SMG-C6 cell line. GFP-LC3 and Lyso-Tracker Red fluorescence probe were used to assess the levels of autophagosomes and lysosome fusion and the effect of BTXA on autophagic flux in SMG-C6. Western blotting and immunofluorescence results showed that BTXA temporarily increased autophagosomes in rat SMG. MTS results showed that BTXA exerted its toxicity on SMG-C6 in a dose-dependent manner. BTXA increased the number of autophagosomes in SMG-C6; however, most autophagosomes did not colocalize with lysosome. Therefore, we presume that BTXA can change autophagic flux of SMG cells, the mechanism of which might relate with BTXA's disturbing autophagosome-lysosome fusion.

Keywords: LC-3; autophagy; autophagy flux; botulinum toxin type A; p62; submandibular gland.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagosomes / metabolism*
  • Autophagosomes / pathology
  • Autophagy / drug effects*
  • Botulinum Toxins, Type A / toxicity*
  • Cell Line
  • Lysosomes / metabolism*
  • Lysosomes / pathology
  • Male
  • Microtubule-Associated Proteins / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Submandibular Gland / metabolism*
  • Submandibular Gland / pathology

Substances

  • LC3 protein, rat
  • Microtubule-Associated Proteins
  • Botulinum Toxins, Type A