scholarly journals PTPσ functions as a presynaptic receptor for the glypican-4/LRRTM4 complex and is essential for excitatory synaptic transmission

2015 ◽  
Vol 112 (6) ◽  
pp. 1874-1879 ◽  
Author(s):  
Ji Seung Ko ◽  
Gopal Pramanik ◽  
Ji Won Um ◽  
Ji Seon Shim ◽  
Dongmin Lee ◽  
...  
Keyword(s):  
Synaptic Transmission ◽  
Synapse Formation ◽  
Transmembrane Protein ◽  
Protein Tyrosine Phosphatases ◽  
Excitatory Synaptic Transmission ◽  
Receptor Protein ◽  
Synapse Development ◽  
Dependent Manner ◽  
And Function ◽  
Receptor Protein Tyrosine Phosphatases

Leukocyte common antigen-related receptor protein tyrosine phosphatases—comprising LAR, PTPδ, and PTPσ—are synaptic adhesion molecules that organize synapse development. Here, we identify glypican 4 (GPC-4) as a ligand for PTPσ. GPC-4 showed strong (nanomolar) affinity and heparan sulfate (HS)-dependent interaction with the Ig domains of PTPσ. PTPσ bound only to proteolytically cleaved GPC-4 and formed additional complex with leucine-rich repeat transmembrane protein 4 (LRRTM4) in rat brains. Moreover, single knockdown (KD) of PTPσ, but not LAR, in cultured neurons significantly reduced the synaptogenic activity of LRRTM4, a postsynaptic ligand of GPC-4, in heterologous synapse-formation assays. Finally, PTPσ KD dramatically decreased both the frequency and amplitude of excitatory synaptic transmission. This effect was reversed by wild-type PTPσ, but not by a HS-binding–defective PTPσ mutant. Our results collectively suggest that presynaptic PTPσ, together with GPC-4, acts in a HS-dependent manner to maintain excitatory synapse development and function.

scholarly journals Intact synapse structure and function after combined knockout of PTPδ, PTPσ and LAR

2021 ◽  
Author(s):  
Javier Emperador-Melero ◽  
Giovanni de Nola ◽  
Pascal S. Kaeser
Keyword(s):  
Active Zone ◽  
Protein Tyrosine Phosphatases ◽  
Conditional Knockout ◽  
Receptor Protein ◽  
Inhibitory Synapses ◽  
Superresolution Microscopy ◽  
Presynaptic Nerve Terminals ◽  
And Function ◽  
Membrane Anchoring ◽  
Receptor Protein Tyrosine Phosphatases

AbstractIt has long been proposed that Leukocyte common Antigen-Related Receptor Protein Tyrosine Phosphatases (LAR-RPTPs) are cell-adhesion proteins for the control of synapse assembly. Their synaptic nanoscale localization, however, has not been established, and the fine structure of synapses after knockout of the three vertebrate genes for LAR-RPTPs (PTPδ, PTPσ and LAR) has not been tested. Here, we find that PTPδ is precisely apposed to postsynaptic scaffolds at excitatory and inhibitory synapses using superresolution microscopy. We generated triple-conditional knockout mice for PTPδ, PTPσ and LAR to test whether they are essential for synapse structure. While mild effects on synaptic vesicle clustering and active zone architecture were detected, synapse numbers and their overall structure were unaffected, membrane anchoring of the active zone persisted, and vesicle docking and release were normal. We conclude that LAR-RPTPs, despite their localization at synaptic appositions, are dispensable for the organization and function of presynaptic nerve terminals.

scholarly journals Type IIa RPTPs and Glycans: Roles in Axon Regeneration and Synaptogenesis

2021 ◽  
Vol 22 (11) ◽  
pp. 5524
Author(s):  
Kazuma Sakamoto ◽  
Tomoya Ozaki ◽  
Yuji Suzuki ◽  
Kenji Kadomatsu
Keyword(s):  
Heparan Sulfate ◽  
Network Formation ◽  
Synapse Formation ◽  
Axon Regeneration ◽  
Transmembrane Protein ◽  
Inhibitory Synapses ◽  
Dependent Manner ◽  
Axon Terminals ◽  
Axon Extension ◽  
Receptor Tyrosine Phosphatases

Type IIa receptor tyrosine phosphatases (RPTPs) play pivotal roles in neuronal network formation. It is emerging that the interactions of RPTPs with glycans, i.e., chondroitin sulfate (CS) and heparan sulfate (HS), are critical for their functions. We highlight here the significance of these interactions in axon regeneration and synaptogenesis. For example, PTPσ, a member of type IIa RPTPs, on axon terminals is monomerized and activated by the extracellular CS deposited in neural injuries, dephosphorylates cortactin, disrupts autophagy flux, and consequently inhibits axon regeneration. In contrast, HS induces PTPσ oligomerization, suppresses PTPσ phosphatase activity, and promotes axon regeneration. PTPσ also serves as an organizer of excitatory synapses. PTPσ and neurexin bind one another on presynapses and further bind to postsynaptic leucine-rich repeat transmembrane protein 4 (LRRTM4). Neurexin is now known as a heparan sulfate proteoglycan (HSPG), and its HS is essential for the binding between these three molecules. Another HSPG, glypican 4, binds to presynaptic PTPσ and postsynaptic LRRTM4 in an HS-dependent manner. Type IIa RPTPs are also involved in the formation of excitatory and inhibitory synapses by heterophilic binding to a variety of postsynaptic partners. We also discuss the important issue of possible mechanisms coordinating axon extension and synapse formation.

scholarly journals Slitrk2 controls excitatory synapse development via PDZ-mediated protein interactions

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Kyung Ah Han ◽  
Jinhu Kim ◽  
Hyeonho Kim ◽  
Dongwook Kim ◽  
Dongseok Lim ◽  
...  
Keyword(s):  
Protein Interactions ◽  
Intracellular Signaling ◽  
Hippocampal Neurons ◽  
Pdz Domain ◽  
Protein Tyrosine Phosphatases ◽  
Excitatory Synapse ◽  
Receptor Protein ◽  
Binding Motif ◽  
Synapse Development

AbstractMembers of the Slitrk (Slit- and Trk-like protein) family of synaptic cell-adhesion molecules control excitatory and inhibitory synapse development through isoform-dependent extracellular interactions with leukocyte common antigen-related receptor protein tyrosine phosphatases (LAR-RPTPs). However, how Slitrks participate in activation of intracellular signaling pathways in postsynaptic neurons remains largely unknown. Here we report that, among the six members of the Slitrk family, only Slitrk2 directly interacts with the PDZ domain-containing excitatory scaffolds, PSD-95 and Shank3. The interaction of Slitrk2 with PDZ proteins is mediated by the cytoplasmic COOH-terminal PDZ domain-binding motif (Ile-Ser-Glu-Leu), which is not found in other Slitrks. Mapping analyses further revealed that a single PDZ domain of Shank3 is responsible for binding to Slitrk2. Slitrk2 forms in vivo complexes with membrane-associated guanylate kinase (MAGUK) family proteins in addition to PSD-95 and Shank3. Intriguingly, in addition to its role in synaptic targeting in cultured hippocampal neurons, the PDZ domain-binding motif of Slitrk2 is required for Slitrk2 promotion of excitatory synapse formation, transmission, and spine development in the CA1 hippocampal region. Collectively, our data suggest a new molecular mechanism for conferring isoform-specific regulatory actions of the Slitrk family in orchestrating intracellular signal transduction pathways in postsynaptic neurons.

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