Involvement of α2-antiplasmin in dendritic growth of hippocampal neurons

J Neurochem. 2013 Jul;126(1):58-69. doi: 10.1111/jnc.12281. Epub 2013 May 22.

Abstract

The α2-Antiplasmin (α2AP) protein is known as a principal physiological inhibitor of plasmin, but we previously demonstrated that it acts as a regulatory factor for cellular functions independent of plasmin. α2AP is highly expressed in the hippocampus, suggesting a potential role for α2AP in hippocampal neuronal functions. However, the role for α2AP was unclear. This study is the first to investigate the involvement of α2AP in the dendritic growth of hippocampal neurons. The expression of microtubule-associated protein 2, which contributes to neurite initiation and neuronal growth, was lower in the neurons from α2AP⁻/⁻ mice than in the neurons from α2AP⁺/⁺ mice. Exogenous treatment with α2AP enhanced the microtubule-associated protein 2 expression, dendritic growth and filopodia formation in the neurons. This study also elucidated the mechanism underlying the α2AP-induced dendritic growth. Aprotinin, another plasmin inhibitor, had little effect on the dendritic growth of neurons, and α2AP induced its expression in the neurons from plaminogen⁻/⁻ mice. The activation of p38 MAPK was involved in the α2AP-induced dendritic growth. Therefore, our findings suggest that α2AP induces dendritic growth in hippocampal neurons through p38 MAPK activation, independent of plasmin, providing new insights into the role of α2AP in the CNS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Cells, Cultured
  • Dendrites / physiology*
  • Fibrinolysin / physiology
  • Hippocampus / cytology*
  • Hippocampus / growth & development*
  • Hippocampus / physiology
  • Immunohistochemistry
  • MAP Kinase Kinase 4 / genetics
  • MAP Kinase Kinase 4 / physiology
  • MAP Kinase Signaling System / genetics
  • MAP Kinase Signaling System / physiology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / physiology
  • Neurons / physiology*
  • Plasminogen / genetics
  • Plasminogen / physiology
  • Real-Time Polymerase Chain Reaction
  • alpha-2-Antiplasmin / physiology*
  • p38 Mitogen-Activated Protein Kinases / genetics
  • p38 Mitogen-Activated Protein Kinases / physiology

Substances

  • Microtubule-Associated Proteins
  • alpha-2-Antiplasmin
  • Plasminogen
  • p38 Mitogen-Activated Protein Kinases
  • MAP Kinase Kinase 4
  • Fibrinolysin