|Year : 2017 | Volume
| Issue : 7 | Page : 1024-1027
BDNF pro-peptide: a novel synaptic modulator generated as an N-terminal fragment from the BDNF precursor by proteolytic processing
Toshiyuki Mizui1, Koji Ohira2, Masami Kojima Ph.D. 3
1 Biomedical Research Inst. (BMD), National Institute of Advanced Industrial Science and Technology (AIST), Osaka; Core Research for Evolutional Science and Technology (CREST), Science and Technology Agency (JST), Kawaguchi, Japan
2 Laboratory of Nutritional Brain Science, Department of Food Science and Nutrition, Mukogawa Women's University, Hyogo, Japan
3 Biomedical Research Inst. (BMD), National Institute of Advanced Industrial Science and Technology (AIST), Osaka; Core Research for Evolutional Science and Technology (CREST), Science and Technology Agency (JST), Kawaguchi; Graduate School of Frontier Bioscience, Osaka University, Suita, Japan
|Date of Acceptance||05-Jul-2017|
|Date of Web Publication||1-Aug-2017|
Biomedical Research Inst. (BMD), National Institute of Advanced Industrial Science and Technology (AIST), Osaka; Core Research for Evolutional Science and Technology (CREST), Science and Technology Agency (JST), Kawaguchi; Graduate School of Frontier Bioscience, Osaka University, Suita
Source of Support: This work was supported by a Grant-in-Aid for Scientific Research on Priority Areas (Elucidation of neural network function in the brain) from the Ministry of Education, Culture, Sports, Science and Technology of Japan: KAKENHI Grant-in-Aid for Scientific Research (17K07073 and 22500305) (MK); Japan Science and Technology Agency; and Core Research for Evolutional Science and Technology (MK)., Conflict of Interest: None
Most growth factors are initially synthesized as precursors and it was cleaved into bioactive mature domain and pro-domain. However, compared with the expression and function of bioactive mature domain, the biological role of the pro-domain is poorly understood. Unexpectedly, we found that the pro-domain (or pro-peptide) of brain-derived neurotrophic factor (BDNF), which is well-known neurotrophic factor in brain, has a potential ability to facilitate hippocampal long-term depression. Furthermore, a BDNF polymorphism Val66Met, which substitute valine into methionine at 66 amino acid, impacted the biological activity of the BDNF pro-peptide. We lastly discuss the possible roles of BDNF and its pro-peptide in the generation of neural stem cells and progress of ischemia.
Keywords: BDNF; growth factor; neural stem cells; ischemia; peptide
|How to cite this article:|
Mizui T, Ohira K, Kojima M. BDNF pro-peptide: a novel synaptic modulator generated as an N-terminal fragment from the BDNF precursor by proteolytic processing. Neural Regen Res 2017;12:1024-7
|How to cite this URL:|
Mizui T, Ohira K, Kojima M. BDNF pro-peptide: a novel synaptic modulator generated as an N-terminal fragment from the BDNF precursor by proteolytic processing. Neural Regen Res [serial online] 2017 [cited 2020 Jul 7];12:1024-7. Available from: http://www.nrronline.org/text.asp?2017/12/7/1024/211173
| Introduction|| |
Brain-derived neurotrophic factor (BDNF) is a well-studied growth hormone that controls numerous complex physiological processes in the nervous system. Herein, we briefly review the role of BDNF, and focus on the novel bioactive BDNF pro-peptide that is generated by proteolytic processing of the proBDNF precursor. Interestingly, the pro-peptide facilitates hippocampal long-term depression, while BDNF reportedly enhances long-term potentiation. Thus, these peptides appear to have opposing biological roles in the nervous system. Recent and future research in this area could provide new insight into the neurobiology and neuropathology of BDNF and related proteins.
| BDNF Functions and Cellular Mechanisms|| |
BDNF is a neurotrophin that is widely distributed in the central nervous system (CNS) and exerts its biological actions by binding to tyrosine kinase receptor TrkB. In developing neurons, BDNF mainly promotes survival and differentiation. During development, however, the biological actions of BDNF extend beyond neuronal survival and differentiation. In mature neurons, BDNF reportedly enhances synaptic transmission and modulates synaptic plasticity. This observation was further supported by genetic and behavioral mouse studies, the results of which indicate that the primary function of BDNF in the adult brain is to control synaptic transmission and plasticity, rather than cell survival. In line with these findings, BDNF expression and secretion is elicited by neuronal activity, a fundamental driving force of neuronal networks. Furthermore, the transcriptional mechanism underlying the activity-dependent expression of BDNF has been thoroughly investigated. Numerous reports implicate impaired BDNF function in cellular mechanisms related to brain diseases. Thus, the molecular and cellular knowledge concerning BDNF, accumulated since its discovery, has gradually illuminated its physiological and pathological roles. For more detailed information, please see a recent review article by Castren and Antila (2017).
| BDNF Pro-peptide is Localized at Presynaptic Dense Core Vesicles in Hippocampal Mossy Fibers|| |
Post-translational mechanisms are known to specify and diversify the actions of growth factors. However, compared with transcription and cell signaling, post-translational mechanisms related to BDNF are less well understood. Like other growth factors, BDNF is initially synthesized as a precursor protein (proBDNF, ~270 amino acids), which is composed of a signal sequence, pro-domain, and mature domain [Figure 1]A. To produce bioactive BDNF, the N-terminal pro-domain (~120 amino acids) is cleaved from proBDNF by intracellular and/or extracellular peptidase enzymes (Lessmann and Brigadski, 2009). In theory, BDNF and its pro-peptide (pro-domain) are produced in equivalent amounts after processing, but the existence of the endogenous pro-peptide had not been detected until recently. Dieni et al. (2012) first demonstrated the endogenous presence of the BDNF pro-peptide by western blotting and immunocytochemistry. Interestingly, in their electro-microscopic study, both BDNF and its pro-peptide were localized in dense core vesicles in excitatory presynaptic terminals of the adult mouse hippocampus, suggesting that they function in the synapse region and are secreted in an anterograde manner.
|Figure 1: BDNF pro-peptide is a novel synaptic modulator generated from the BDNF precursor and Val66Met BDNF polymorphism located in the BDNF pro-peptide-dependent exerts distinct functions in LTD. |
(A) The BDNF pro-peptide is generated by proteolytic processing of proBDNF. The N-terminus fragment is shown to be localized at presynaptic dense core vesicles (Dieni et al., 2012) and secreted from cultured hippocampal neurons (Anastasia et al., 2013; Mizui et al., 2015). (B) At hippocampal CA1–CA3 synaptic junctions, valine-type BDNF pro-peptide facilitates LFS-induced hippocampal LTD and induces endocytosis of GluA2, a crucial mechanism of LTD expression (middle). However, methionine-type pro-peptide attenuates LTD and the underlying mechanism, endocytosis of GluA2 is reversed by the mutated pro-peptide (right). This figure summarizes our recent findings (Mizui et al., 2015). AMPAR: α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor; BDNF: brain-derived neurotrophic factor; LTD: long-term depression; NMDAR: N-methyl-D-aspartate receptor; TrkB: tyrosine receptor kinase B.
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| BDNF Pro-peptide is a Novel Facilitator of Long-Term Depression (LTD)|| |
Although the BDNF pro-peptide corresponds to the N-terminal fragment of proBDNF, we found that it functions as a modulator of synaptic plasticity by enhancing hippocampal LTD (Mizui et al., 2015). In our study, we applied a sequence of low-frequency stimulation (LFS) pulses (900 pulses, 1 Hz, 15 minutes) to Schaffer collaterals of hippocampal slices prepared from 3–4-week-old juvenile mice, and measured field excitatory postsynaptic potential (fEPSP) slopes in the CA1 area. We showed that a 30-minute treatment with the BDNF pro-peptide (10 ng/mL) enhances LTD without affecting basal synaptic transmission, and a sub-nanomolar concentration of BDNF pro-peptide is sufficient for LTD enhancement ([Figure 1]B, Val-BDNF pro-peptide + LFS). Additionally, application of the BDNF pro-peptide to Bdnf–/– hippocampal slices facilitates LTD, confirming the role of the pro-peptide as a ligand. This work also revealed mechanistic details; BDNF pro-peptide-dependent LTD facilitation requires the activation of GluN2B-containing N-methyl-D-aspartate (NMDA) receptors and the pan-neurotrophin receptor p75NTR. In a study using Banker-style primary cultures of hippocampal neurons, BDNF pro-peptide promoted NMDA-induced α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor endocytosis, a critical mechanism for LTD expression. More recently, it was demonstrated that exposure of mature hippocampal neurons to the BDNF pro-peptide dramatically reduced dendritic spine density in vitro (Guo et al., 2016). Interestingly, this effect was mediated by caspase-3, and BDNF pro-peptide increased the number of elongated mitochondria and the amount of cytosolic cytochrome c, indicating the involvement of the mitochondrial-caspase-3 pathway in the BDNF pro-peptide-induced decrease in spine density. BDNF pro-peptide has also recently been linked to growth cones (Anastasia et al., 2013) and LTD (Mizui et al., 2015), suggesting that it may act as a negative regulator of neuronal structure and function at distinct developmental stages.
| Molecular Role of the Common Val66Met BDNF Polymorphism|| |
There is a body of evidence speculating on the impact of the common Val66Met BDNF polymorphism in human brain functions and diseases (Notaras et al., 2015). Several reports focused on the molecular outcome of this amino acid substitution. We previously showed that the Val66Met polymorphism impairs intracellular trafficking of BDNF (Egan et al., 2003). It was next reported that the Vps10p protein sortilin interacts with the BDNF pro-domain, and the Val66Met mutation stimulated the interaction of the BDNF pro-domain with BDNF rather than with sortilin (Chen et al., 2005). Furthermore, we recently quantitatively demonstrated that the Val66Met mutation enhanced the stability of the complex between BDNF and its pro-peptide using surface plasmon resonance, and found that the interaction is stronger in acidic conditions (Uegaki et al., 2017). In another report, hippocampal slices prepared from mice with the Val66Met mutation revealed defective NMDAR-dependent synaptic plasticity (Ninan et al., 2010). Interestingly, our recent report showed that the BDNF pro-peptide-induced LTD and its mechanism endocytosis of GluA2, was reversed by the mutated BDNF pro-peptide ([Figure 1]B, Met-BDNF pro-peptide + LFS) (Mizui et al., 2015). These findings together suggest that the Val66Met polymorphism impacts the cellular activity of BDNF and the BDNF pro-peptide. In the future, it will be interesting to investigate the impact of the Val66Met BDNF polymorphism at the level of neuronal circuits, and probe the mechanistic influence in brain diseases.
| Development of Potential New Therapies for Brain Diseases Based on BDNF and Related Proteins|| |
The roles of BDNF and related proteins in human neurological and neuropsychiatric disorders are receiving increasing attention, and new BDNF-related diagnostic tools and treatments are anticipated. Lim et al. (2015) measured the concentration of BDNF pro-peptide and mature BDNF in extracts of age-matched postmortem hippocampal samples from patients with advanced Alzheimer's disease (AD; Braak Stages 5–6) and healthy individuals, and found that the BDNF pro-peptide was markedly elevated in AD patients (Lim et al., 2015). Furthermore, in postmortem brain samples of AD patients, the abundance of full-length p75NTR (p75NTRFL) was increased, while the extracellular domain (p75NTRECD) that is released following cleavage by α-secretase was decreased (Yao et al., 2015). Taken together with our observation that the BDNF pro-peptide enhances hippocampal LTD through the activation of p75NTR (Mizui et al., 2015), the current neurological knowledge may lead to the development of new drug treatments for AD.
Adult neurogenesis in the subventricular zone (SVZ) and hippocampal dentate gyrus has been demonstrated in studies going back to the 1960s. In these regions, there are neural stem cells (NSCs) and neural progenitor cells (NPCs), which might be the cellular basis for endogenous regenerative therapy for brain damage. It was demonstrated that NPCs were detectable in the cortex, and their ability to produce new neurons was activated after brain ischemia (Ohira et al., 2010) and antidepressant treatments (Ohira et al., 2013). Additionally, new-born neurons possessed neuroprotective activity by inhibiting neuronal cell death via glutamate excitotoxicity in ischemia (Ohira et al., 2013).
Previously, it was demonstrated that brain ischemia elicits BDNF expression (Lindvall et al., 1994) and adult neurogenesis (Liu et al., 1998). A recent report shows that NSCs and NPCs express neurotrophin receptors, p75NTR and Trk receptors, and neurotrophin signaling could control proliferation and differentiation of NSCs and NPCs (Vilar and Mira, 2016; Castren and Antila, 2017). Taken together, BDNF signaling might undergo neuroprotective and neuroregerative actions of NPCs against ischemia, while the BDNF pro-peptide (Anastasia et al., 2013; Mizui et al., 2015; Guo et al., 2016) may exert pathological action on NPCs and progressive role on ischemia.
Herein, we reviewed the role of the BDNF pro-peptide that corresponds to the N-terminus of proBDNF following cleavage by proteolytic processing. The BDNF pro-peptide is detectable in multiple cell and tissue types and elicits hippocampal LTD and spine pruning. Moreover, an interesting recent study showed that the BDNF pro-peptide is more abundant in the brain during development, and appears to control growth cone collapse (Anastasia et al., 2013). Thus, a new ligand-based model, in which BDNF and its pro-peptide exert distinct biological functions, could provide novel insight into the biology of neurotrophins and support the development of new therapies for brain diseases.
| References|| |
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Author contributions: TM and MK made equal contributions to this paper as co- first authors. KO made contributions to the discussion on neural stem cells and brain diseases.
Conflicts of interest: None declared.
Contributor agreement: A statement of “Publishing Agreement” has been signed by an authorized author on behalf of all authors prior to publication.
Plagiarism check: This paper has been checked twice with duplication-checking software iThenticate.
Peer review: A double-blind and stringent peer review process has been performed to ensure the integrity, quality and significance of this paper.
Open peer review report:
Reviewer: Giovanni Casini, Universita degli Studi di Pisa, Italy.
Comments to author: This paper is a concise, very clear and up-to-date commentary on the physiology of BDNF pro-peptide. The research focusing on this peptide is relatively new and this paper makes sets the state of the art of such research field.
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