Nucleus-translocated matrix metalloprotease 1 regulates innate immune response in Pacific abalone (Haliotis discus

Yu-Lei Chen1, Wan-Yu Li1, Jian-Jian Hu1

  • 1College of Food and Biological Engineering, Jimei University, Xiamen, Fujian Province, 361021, China.

Insights

Pacific abalone immunity against Vibrio parahemolyticus infection involves matrix metalloproteinase-1 (MMP-1). MMP-1 regulates key immune genes and cellular functions, acting as an upstream factor in abalone

Area of Science:

  • Marine biology
  • Invertebrate immunology
  • Shellfish aquaculture

Background:

  • Abalone, an economically important shellfish, faces significant threats from bacterial infections like Vibrio parahemolyticus.
  • Matrix metalloproteinases (MMPs) are crucial in mammalian immunity, but their role in abalone innate immunity remains largely unexplored.

Purpose of the Study:

  • To investigate the function of MMP-1 in the Pacific abalone (Haliotis discus hannai) immune response to Vibrio parahemolyticus infection.
  • To elucidate the regulatory role of MMP-1 in abalone innate immunity.

Main Methods:

  • Gene expression analysis of MMP-1 and related immune genes (AIF-1, MPEG-1, Tis11FP) following V. parahemolyticus challenge.
  • RNA interference (RNAi) to silence MMP-1 expression and assess its impact on immune gene expression.
  • Evaluation of MMP-1's role in cellular immunity (phagocytosis, apoptosis) and humoral immunity (SOD, ALP, ACP activity).

Main Results:

  • V. parahemolyticus infection significantly upregulated MMP-1 expression and other immune genes.
  • Silencing MMP-1 reduced the expression of these immune genes, indicating MMP-1's upstream regulatory role.
  • MMP-1 was involved in regulating cellular and humoral immune responses, with extracellular MMP-1 translocating to hemocyte nuclei.

Conclusions:

  • MMP-1 plays a critical role in the innate immune defense of Pacific abalone against V. parahemolyticus.
  • This study provides the first evidence of MMP involvement in abalone immunity, highlighting MMP-1 as a potential therapeutic target.

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