Articles producció científica> Ciències Mèdiques Bàsiques

Opposed Actions of PKA Isozymes (RI and RII) and PKC Isoforms (cPKC beta I and nPKC epsilon) in Neuromuscular Developmental Synapse Elimination

  • Dades identificatives

    Identificador: imarina:6013681
    Autors:
    Garcia, NeusBalana, CoriLanuza, Maria ATomas, MartaCilleros-Mane, VictorJust-Borras, LaiaTomas, Josep
    Resum:
    Background: During neuromuscular junction (NMJ) development, synapses are produced in excess. By sensing the activity-dependent release of ACh, adenosine, and neurotrophins, presynaptic receptors prompt axonal competition and loss of the unnecessary axons. The receptor action is mediated by synergistic and antagonistic relations when they couple to downstream kinases (mainly protein kinases A and C (PKA and PKC)), which phosphorylate targets involved in axonal disconnection. Here, we directly investigated the involvement of PKA subunits and PKC isoforms in synapse elimination. Methods: Selective PKA and PKC peptide modulators were applied daily to the Levator auris longus (LAL) muscle surface of P5-P8 transgenic B6.Cg-Tg (Thy1-YFP) 16 Jrs/J (and also C57BL/6J) mice, and the number of axons and the postsynaptic receptor cluster morphology were evaluated in P9 NMJ. Results: PKA (PKA-I and PKA-II isozymes) acts at the pre- and postsynaptic sites to delay both axonal elimination and nAChR cluster differentiation, PKC activity promotes both axonal loss (a cPKC beta I and nPKC epsilon isoform action), and postsynaptic nAChR cluster maturation (a possible role for PKC theta). Moreover, PKC-induced changes in axon number indirectly influence postsynaptic maturation. Conclusions: PKC and PKA have opposed actions, which suggests that changes in the balance of these kinases may play a major role in the mechanism of developmental synapse elimination.
  • Altres:

    Autor segons l'article: Garcia, Neus; Balana, Cori; Lanuza, Maria A; Tomas, Marta; Cilleros-Mane, Victor; Just-Borras, Laia; Tomas, Josep
    Departament: Ciències Mèdiques Bàsiques
    e-ISSN: 2073-4409
    Autor/s de la URV: Cilleros Mañé, Víctor / Garcia Sancho, Maria de les Neus / Just Borràs, Laia / Lanuza Escolano, María Angel / Tomas Marginet, Marta / Tomàs Porres, Josep
    Paraules clau: Trkb receptors Synapses Signal transduction Serine kinases Receptors, purinergic p1 Receptors, muscarinic Protein-kinase-c Protein kinase c Protein isoforms Presynaptic muscarinic receptors Postsynaptic maturation Postnatal synapse elimination Pkc Pka Phosphorylation Nicotinic acetylcholine-receptor Neurotransmitter release Neuromuscular junction Muscle, skeletal Muscarinic acetylcholine receptors Motor endplate Motor end-plate Modulate transmitter release Mice, transgenic Mice, inbred c57bl Mice Male Isoenzymes Functional elimination Cyclic amp-dependent protein kinases Cell differentiation Calcium-channels Axons Animals Adenosine receptors Acetylcholine release Acetylcholine trkb receptors pkc pka muscarinic acetylcholine receptors motor end-plate adenosine receptors acetylcholine release
    Resum: Background: During neuromuscular junction (NMJ) development, synapses are produced in excess. By sensing the activity-dependent release of ACh, adenosine, and neurotrophins, presynaptic receptors prompt axonal competition and loss of the unnecessary axons. The receptor action is mediated by synergistic and antagonistic relations when they couple to downstream kinases (mainly protein kinases A and C (PKA and PKC)), which phosphorylate targets involved in axonal disconnection. Here, we directly investigated the involvement of PKA subunits and PKC isoforms in synapse elimination. Methods: Selective PKA and PKC peptide modulators were applied daily to the Levator auris longus (LAL) muscle surface of P5-P8 transgenic B6.Cg-Tg (Thy1-YFP) 16 Jrs/J (and also C57BL/6J) mice, and the number of axons and the postsynaptic receptor cluster morphology were evaluated in P9 NMJ. Results: PKA (PKA-I and PKA-II isozymes) acts at the pre- and postsynaptic sites to delay both axonal elimination and nAChR cluster differentiation, PKC activity promotes both axonal loss (a cPKC beta I and nPKC epsilon isoform action), and postsynaptic nAChR cluster maturation (a possible role for PKC theta). Moreover, PKC-induced changes in axon number indirectly influence postsynaptic maturation. Conclusions: PKC and PKA have opposed actions, which suggests that changes in the balance of these kinases may play a major role in the mechanism of developmental synapse elimination.
    Àrees temàtiques: Medicine (miscellaneous) Cell biology Biochemistry, genetics and molecular biology (miscellaneous) Biochemistry, genetics and molecular biology (all)
    Accès a la llicència d'ús: https://creativecommons.org/licenses/by/3.0/es/
    ISSN: 20734409
    Adreça de correu electrònic de l'autor: josep.tomas@urv.cat laia.just@urv.cat marta.tomas@urv.cat josep.tomas@urv.cat victor.cilleros@alumni.urv.cat laia.just@urv.cat mariaangel.lanuza@urv.cat
    Identificador de l'autor: 0000-0003-0473-3730 0000-0002-4151-1697 0000-0001-5690-9932 0000-0003-0473-3730 0000-0003-4795-4103
    Data d'alta del registre: 2024-10-12
    Volum de revista: 8
    Versió de l'article dipositat: info:eu-repo/semantics/publishedVersion
    Enllaç font original: https://www.mdpi.com/2073-4409/8/11/1304
    URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/
    Referència a l'article segons font original: Cells. 8 (11): E1304-
    Referència de l'ítem segons les normes APA: Garcia, Neus; Balana, Cori; Lanuza, Maria A; Tomas, Marta; Cilleros-Mane, Victor; Just-Borras, Laia; Tomas, Josep (2019). Opposed Actions of PKA Isozymes (RI and RII) and PKC Isoforms (cPKC beta I and nPKC epsilon) in Neuromuscular Developmental Synapse Elimination. Cells, 8(11), E1304-. DOI: 10.3390/cells8111304
    DOI de l'article: 10.3390/cells8111304
    Entitat: Universitat Rovira i Virgili
    Any de publicació de la revista: 2019
    Tipus de publicació: Journal Publications
  • Paraules clau:

    Biochemistry, Genetics and Molecular Biology (Miscellaneous),Cell Biology,Medicine (Miscellaneous)
    Trkb receptors
    Synapses
    Signal transduction
    Serine kinases
    Receptors, purinergic p1
    Receptors, muscarinic
    Protein-kinase-c
    Protein kinase c
    Protein isoforms
    Presynaptic muscarinic receptors
    Postsynaptic maturation
    Postnatal synapse elimination
    Pkc
    Pka
    Phosphorylation
    Nicotinic acetylcholine-receptor
    Neurotransmitter release
    Neuromuscular junction
    Muscle, skeletal
    Muscarinic acetylcholine receptors
    Motor endplate
    Motor end-plate
    Modulate transmitter release
    Mice, transgenic
    Mice, inbred c57bl
    Mice
    Male
    Isoenzymes
    Functional elimination
    Cyclic amp-dependent protein kinases
    Cell differentiation
    Calcium-channels
    Axons
    Animals
    Adenosine receptors
    Acetylcholine release
    Acetylcholine
    trkb receptors
    pkc
    pka
    muscarinic acetylcholine receptors
    motor end-plate
    adenosine receptors
    acetylcholine release
    Medicine (miscellaneous)
    Cell biology
    Biochemistry, genetics and molecular biology (miscellaneous)
    Biochemistry, genetics and molecular biology (all)
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