Cleavage of proBDNF by tPA/Plasmin Is Essential for Long-Term Hippocampal Plasticity

Author:

Pang Petti T.123,Teng Henry K.123,Zaitsev Eugene123,Woo Newton T.123,Sakata Kazuko123,Zhen Shushuang123,Teng Kenneth K.123,Yung Wing-Ho123,Hempstead Barbara L.123,Lu Bai123

Affiliation:

1. Section on Neural Development and Plasticity, Laboratory of Cellular and Synaptic Neurophysiology, National Institute of Child Health and Human Development (NICHD), Bethesda, MD 20892, USA.

2. Division of Hematology, Department of Medicine, Weill Medical College of Cornell University, New York, NY 10021, USA.

3. Department of Physiology, Faculty of Medicine, Chinese University of Hong Kong, Shatin, New Territories, Hong Kong.

Abstract

Long-term memory is thought to be mediated by protein synthesis–dependent, late-phase long-term potentiation (L-LTP). Two secretory proteins, tissue plasminogen activator (tPA) and brain-derived neurotrophic factor (BDNF), have been implicated in this process, but their relationship is unclear. Here we report that tPA, by activating the extracellular protease plasmin, converts the precursor proBDNF to the mature BDNF (mBDNF), and that such conversion is critical for L-LTP expression in mouse hippocampus. Moreover, application of mBDNF is sufficient to rescue L-LTP when protein synthesis is inhibited, which suggests that mBDNF is a key protein synthesis product for L-LTP expression.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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