Possible glutaminergic interaction between the capsule and neurite of Pacinian corpuscles

References

• Andres KH, von During M. Morphology of cutaneous receptors. Handbook of sensory physiology. II. Somatosensory system, WR Lowenstein. Springer, Berlin 1973; 3–28
   Google Scholar
• Araque A, Carmignoto G, Haydon PG. Dynamic signaling between astrocytes and neurons. Annu Rev Physiol 2001; 63: 795–813
   PubMed Web of Science ®Google Scholar
• Araque A, Li N, Doyle RT, Haydon PG. SNARE protein-dependent glutamate release from astrocytes. J Neurosci 2000; 20: 666–673
   PubMed Web of Science ®Google Scholar
• Bell J, Bolanowski S, Holmes MH. The structure and function of Pacinian corpuscles: A review. Prog Neurobiol 1994; 42: 79–128
   PubMed Web of Science ®Google Scholar
• Bell J, Holmes MH. Model of the dynamics of receptor potential in a mechanoreceptor. Math Biosci 1992; 110: 139–174
   PubMed Web of Science ®Google Scholar
• Bewick GS, Reid B, Richardson C, Banks RW. Autogenic modulation of mechanoreceptor excitability by glutamate release from synaptic-like vesicles: Evidence from rat muscle spindle primary sensory ending. J Physiol 2005; 562(2)381–394
   PubMedGoogle Scholar
• Bezzi P, Galbete J, Gundersen V, Pilati E, Stubbe BH, Volterra A. Vesicular glutamate exocytosis in astrocytes. Dynamic imaging and ultrastructural evidence. Society for Neuroscience, Washington, DC 2003, Program No. 691.10.2003 Abstract Viewer/Itinerary Planner
   Google Scholar
• Bolanowski Jr SJ. Intensity and frequency characteristics of Pacinian corpuscles. III. Effects of tetrodotoxin on transduction process. J Neurophysiol 1984; 51: 831–839
   PubMedGoogle Scholar
• Bolanowski SJ. Transduction mechanisms in Pacinian corpuscles. Mechanoreceptors: Development, structure and function, TSP Hnik, R Vejsada, J Zelena. Plenum, New York 1988; 201–207
   Google Scholar
• Bolanowski SJ, Schyuler JE, Slepecky NB. Semi-serial electron-micrographic reconstruction of putative transducer sites in Pacinian corpuscles. Somatosens Mot Res 1994; 11: 205–218
   PubMed Web of Science ®Google Scholar
• Bolanowski SJ, Schyuler JE, Sulitka D, Pietras B. Mitochondrial distribution within the terminal neurite of the Pacinian corpuscle. Somatosens Mot Res 1996; 13: 49–58
   PubMed Web of Science ®Google Scholar
• Bolanowski SJ, Jr, Zwislocki JJ. Intensity and frequency characteristics of Pacinian Corpuscles. I. Action potentials. J Neurophysiol 1984a; 51: 793–811
   PubMed Web of Science ®Google Scholar
• Bolanowski SJ, Jr, Zwislocki JJ. Intensity and frequency characteristics of Pacinian Corpuscles. II. Receptor potentials. J Neurophysiol 1984b; 51: 812–830
   PubMed Web of Science ®Google Scholar
• Brown AG, Fyffe REW, Noble R. Projections from Pacinian corpuscles and rapidly adapting mechanoreceptors of glabrous skin to the cat's spinal cord. J Physiol 1980; 307: 385–400
   PubMedGoogle Scholar
• Cahusac PMB, Senok SS. Metabotropic glutamate receptor antagonists selectively enhance responses of slowly adapting Type I mechanoreceptors. Synapse 2006; 59: 235–242
   PubMed Web of Science ®Google Scholar
• Carmignoto G. Reciprocal communication systems between astrocytes and neurones. Prog Neurobiol 2000; 62: 561–581
   PubMed Web of Science ®Google Scholar
• Cauna N. The effects of age on the receptor organs of the human dermis. Advances in biology of skin. Vol. VI: Aging, W Monotagna. Pergamon, New York 1965; 63–96
   Google Scholar
• Cauna N, Mannan G. The structure of human digital Pacinian corpuscles (corpuscula lamellosa) and its functional significance. J Anat 1958; 92: 1–25
   PubMed Web of Science ®Google Scholar
• Charles AC, Merrill JE, Dirksen ER, Sanderson MJ. Intercellular signaling in glial cells: Calcium waves and oscillations in response to mechanical stimulation and glutamate. Neuron 1991; 6: 983–992
   PubMed Web of Science ®Google Scholar
• Chiu SY. Sodium currents in axon-associated Schwann cells from adult rabbits. J Physiol 1987; 386: 181–203
   PubMedGoogle Scholar
• Chiu SY. Functions and distribution of voltage-gated sodium and potassium channels in mammalian Schwann cells. Glia 1991; 4: 541–558
   PubMedGoogle Scholar
• Chiu SY. Differential expression of sodium channels in acutely isolated myelinating and non-myelinating Schwann cells of rabbit. J Physiol 1993; 470: 485–499
   PubMedGoogle Scholar
• Chiu SY, Schrager P, Ritchie JM. Neuronal-type Na+ and K+ channels in rabbit cultured Schwann cells. Nature 1984; 311: 156–157
   PubMedGoogle Scholar
• Cornell-Bell AH, Finkbeiner SM, Cooper MS, Smith SJ. Glutamate induces calcium waves in cultured astrocytes: Long-range glial signaling. Science 1990; 247: 470–473
   PubMed Web of Science ®Google Scholar
• Crippa D, Zonta M, Domenici L, Merighi A, Pozzan T, Carmignoto G. Regulated exocytosis of GFP-synaptobrevin tagged vesicles in cultured astrocytes. Program No. 691.13.2003 Abstract Viewer/Itinerary Planner. Society for Neuroscience, Washington, DC 2003
   Google Scholar
• Dermietzel R, Hertzberg EL, Kessler JA, Spray DC. Gap junctions between cultured astrocytes: Immunocytochemical, molecular, and electrophysiological analysis. J Neurosci 1991; 11: 1421–1432
   PubMed Web of Science ®Google Scholar
• Fagan BM, Cahusac PMB. Evidence for glutamate receptor mediated t ransmission at mechanoreceptors in the skin. Neuroreport 2001; 12: 341–347
   PubMed Web of Science ®Google Scholar
• Fields RD. The other half of the brain. Sci Am 2004; 290: 54–61
   PubMedGoogle Scholar
• Grandori F, Pedotti A. Theoretical analysis of mechano-to-neural transduction in Pacinian corpuscle. IEEE Trans Biomed Eng 1980; BME-27: 559–565
   Web of Science ®Google Scholar
• Grandori F, Pedotti A. A mathematical model of the Pacinian corpuscle. Biol Cybern 1982; 46: 7–16
   PubMed Web of Science ®Google Scholar
• Haeberle H, Fujiwara M, Chuang J, Medina MM, Panditrao MV, Bechstedt S, Howard J, Lumpkin EA. Molecular profiling reveals synaptic release machinery in Merkel cells. PNAS 2004; 101: 14503–14508
   PubMed Web of Science ®Google Scholar
• Hepp R, Perraut M, Chasserot-Golaz S, Galli T, Aunis D, Langley K, Grant NJ. Cultured glial cells express the SNAP-25 analogue SNAP-23. Glia 1999; 27: 181–187
   PubMed Web of Science ®Google Scholar
• Hitchcock IS, Genever PG, Cahusac PMB. Essential components for a glutamatergic synapse between Merkel cell and nerve terminal in rats. Neurosci Lett 2004; 362: 196–199
   PubMed Web of Science ®Google Scholar
• Hubbard SJ. The mechanical properties of Pacinian corpuscles. J Physiol Lond 1958; 141: 117–131
   Google Scholar
• Ide C, Hayashi S. Specializations of plasma membranes in Pacinian corpuscles: Implications for mechano-electric transduction. J Neurocytol 1987; 16: 759–773
   PubMedGoogle Scholar
• Ide C, Yoshida Y, Hayashi S, Takashio M, Munger BL. A re-evaluation of the cytology of cat Pacinian corpuscles II. The extreme tip of the axon. Cell Tissue Res 1988; 253: 95–103
   PubMedGoogle Scholar
• Ilyinski OB, Krylov BV, Cherepnov VL. Study of an optimal form of nerve ending of encapsulated tissue mechanoreceptor (Pacinian corpuscle). Neurophysiologia 1976a; 9: 423–428
   Google Scholar
• Ilyinski OB, Volkova NK, Cherepnov VL, Krylov BV. Morphofunctional properties of Pacinian corpuscles. Progress in brain research: Somatosensory and visceral receptor mechanisms, A Iggo, OB Iyinski. Elsevier, Amsterdam 1976b; 173–186
   Google Scholar
• Innocenti B, Parpura V, Haydon PG. Imaging extracellular waves of glutamate during calcium signaling in cultured astrocytes. J Neurosci 2000; 20: 1800–1808
   PubMed Web of Science ®Google Scholar
• Irnich D, Burgstahler R, Bostock H, Grafe P. ATP affects both axons and Schwann cells of unmyelinated C fibers. Pain 2001; 92: 343–350
   PubMedGoogle Scholar
• Iwanaga T, Fujita T, Takahashi Y, Nakajima T. Meissner's and Pacinian corpuscles as studied by immunohistochemistry for S-100 protein, neuron-specific enolase and neurofilament protein. Neurosci Lett 1982; 31: 117–121
   PubMed Web of Science ®Google Scholar
• Jeftinija SD, Jeftinija KV. ATP stimulates release of excitatory amino acids from cultured Schwann cells. Neuroscience 1998; 82: 927–934
   PubMedGoogle Scholar
• Konishi T. Voltage-dependent potassium channels in mouse Schwann cells. J Physiol 1989; 411: 115–130
   PubMedGoogle Scholar
• Konishi T. Voltage-gated potassium currents in myelinating Schwann cells in the mouse. J Physiol 1990; 431: 123–139
   PubMedGoogle Scholar
• Li W, Spray DC. Inhibition of gap junctional communication between astrocytes by thrombin and tumor necrosis factor-α. Program No. 691.18.2003 Abstract Viewer/Itinerary Planner. Society for Neuroscience, Washington, DC 2003
   Google Scholar
• Loewenstein WR, Rathcamp R. Mechano-electric transduction in the Pacinian corpuscle. Initiation of sensory impulses in mechanoreceptors. Handbook of sensory physiology. I. Principles of receptor physiology, WR Loewenstein. Springer, Berlin 1971; 269–290
   Google Scholar
• Lowenstein WR, Skalak R. Mechanical transmission in a Pacinian corpuscle. An analysis of a theory. J Physiol Lond 1966; 182: 346–378
   Google Scholar
• Madison DL, Krueger WH, Cheng D, Trapp BD, Pfeiffer SE. SNARE complex proteins, including the cognate pair VAMP-2 and syntaxin-4 are expressed in cultured oligodendrocytes. J Neurochem 1999; 72: 988–998
   PubMedGoogle Scholar
• Malinovsky L, Pac L, Vega-Alvarez JA, Bozilow W. The capsule structure of Pacinian corpuscles from the cat mesentery. Z mikrosk-anat Forsch 1990; 104: 193–201
   PubMedGoogle Scholar
• Mennerick S, Zorumski CF. Glial contributions to excitatory neurotransmission in cultured hippocampal cells. Nature 1994; 368: 59–62
   PubMed Web of Science ®Google Scholar
• Mi H, Deerinck TJ, Jones M, Ellisman MH, Schwartz TL. Inwardly rectifying K+ channels that may participate in K+ buffering are localized in microvilli of Schwann cells. J Neurosci 1996; 16: 2421–2429
   PubMedGoogle Scholar
• Nedergaard M. Direct signaling from astrocytes to neurons in cultures of mammalian brain cells. Science 1994; 263: 1768–1771
   PubMed Web of Science ®Google Scholar
• Newman EA. Glial cell inhibition of neurons by release of ATP. J Neurosci 2003; 23: 1659–1666
   PubMed Web of Science ®Google Scholar
• Nunzi M-G, Pisarek A, Mugnani E. Merkel cells, corpuscular nerve endings and free nerve endings in the mouse palatine mucosa express three subtypes of vesicular glutamate transporters. J Neurocytol 2004; 33: 359–376
   PubMedGoogle Scholar
• Paemeleire K, Leybaert L. Ionic changes accompanying astrocytic intercellular calcium waves triggered by mechanical cell damaging stimulation. Brain Res 2000; 857: 235–245
   PubMed Web of Science ®Google Scholar
• Parpura V, Basarsky TA, Liu F, Jeftinija K, Jeftinija S, Haydon PG. Glutamate-mediated astrocyte-neuron signaling. Nature 1994; 369: 744–747
   PubMed Web of Science ®Google Scholar
• Parri HR, Crunelli V. The role of Ca2+ in the generation of spontaneous astrocytic Ca2+ oscillations. Neuroscience 2003; 120: 979–992
   PubMedGoogle Scholar
• Pawson L, Bolanowski SJ. Voltage-gated sodium channels are present on both the neural and capsular structures of Pacinian corpuscles. Somatosens Mot Res 2002; 19: 231–237
   PubMed Web of Science ®Google Scholar
• Pawson L, Bolanowski SJ. Positive immunoreactivity for glutamate receptors in Pacinian corpuscles. Program No. 639.3.2004 Abstract Viewer/Itinerary Planner. Society for Neuroscience, Washington, DC 2004
   Google Scholar
• Pawson L, Bolanowski SJ, Verrillo RT. Voltage-gated potassium channels (VG-K) on the lamellae of Pacinian corpuscles (PCs). Program No. 348.8.2002 Abstract Viewer/Itinerary Planner. Society for Neuroscience (CD-ROM), Washington, DC 2002
   Google Scholar
• Pawson L, Slepecky NB, Bolanowski SJ. Immunocytochemical identification of proteins within the Pacinian corpuscle. Somatosens Mot Res 2000; 17: 159–170
   PubMedGoogle Scholar
• Pease DC, Quilliam TA. Electron microscopy of the Pacinian corpuscle. J Biophys Biochem Cytol 1957; 3: 331–342
   PubMedGoogle Scholar
• Piet R, Vargova L, Sykova E, Poulain DA, Oliet SHR. Physiological contribution of the astrocytic environment of neurons to intersynaptic crosstalk. PNAS 2004; 101: 2151–2155
   PubMedGoogle Scholar
• Porter JT, McCarthy KD. Hippocampal astrocytes in situ respond to glutamate released from synaptic terminals. J Neurosci 1996; 16: 5073–5081
   Google Scholar
• Ritchie JM. Sodium-channel turnover in rabbit cultured Schwann cells. Proc R Soc Lond B 1988; 233: 423–430
   PubMedGoogle Scholar
• Ritchie JM, Black JA, Waxman SG, Angelides KJ. Sodium channels in the cytoplasm of Schwann cells. Proc Natl Acad Sci USA 1990; 87: 9290–9294
   PubMed Web of Science ®Google Scholar
• Rouach N, Glowinski J, Giaume C. Activity-dependent neuronal control of gap-junctional communication in astrocytes. J Cell Biol 2000; 149: 1513–1526
   PubMed Web of Science ®Google Scholar
• Santini M. The “receptripse”: The desmosome-like lamellae-axonal junction subserving mechano-electric transduction and effecting the sympathetic actions on the Pacinian sensor. Sensory functions of the skin of primates, with special refrence to man, Y Zotterman. Pergamon, Oxford 1976; 37–42
   Google Scholar
• Seyfarth EA, Sanders EJ, French AS. Sodium channel distribution in a spider mechanosensory organ. Brain Res 1995; 638: 93–101
   Google Scholar
• Shanthaveerappa TR, Bourne GH. Perineural epithelium: A new concept of its role in the integrity of the peripheral nervous system. Science 1966; 154: 1464–1467
   PubMed Web of Science ®Google Scholar
• Shrager P, Chiu SY, Ritchie JM. Voltage-dependent sodium and potassium channels in mammalian cultured Schwann cells. Proc Natl Acad Sci USA 1985; 82: 948–952
   PubMed Web of Science ®Google Scholar
• Spencer PS, Schaumburg HH. An ultrastructural study of the inner core of the Pacinian corpuscle. J Neurocytol 1973; 2: 217–235
   PubMedGoogle Scholar
• Stout CE, Costantin JL, Naus CCG, Charles AC. Intercellular calcium signaling in astrocytes via ATP release through connexin hemichannels. J Biol Chem 2002; 277: 10482–10488
   PubMed Web of Science ®Google Scholar
• Tachibana T, Endoh M, Kumakami R, Nawa T. Immunohistochemical expressions of mGluR5, P2Y2 receptor, PLC-β1, and IP3R-I and II in Merkel cells in rat sinus hair follicles. Histochem Cell Biol 2003; 120: 13–21
   PubMed Web of Science ®Google Scholar
• Vega JA, Zubizarreta JJF, Del Valle ME, Hernandez LC, Bengoechea ME, Perez-Casas A. Immunohistochemical study of the cat Pacinian corpuscles: Co-localization of Vimentin- and S-100 protein-like in the inner core. Cell Mol Biol 1990; 36: 415–420
   PubMed Web of Science ®Google Scholar
• Verkhratsky A, Steinhauser C. Ion channels in glial cells. Brain Res Rev 2000; 32: 380–412
   PubMed Web of Science ®Google Scholar
• Volknandt W. Vesicular release mechanisms in astrocytic signaling. Neurochem Int 2002; 41: 301–306
   PubMedGoogle Scholar
• Volknandt W, Wilhelm A, Nolte C, Kettenmann H, Zimmermann H. Organellar association of t-SNAREs and synaptic proteins in EGFP-expressing astrocytes in vitro and in situ. Program No. 691.11.2003 Abstract Viewer/Itinerary Planner. Society for Neuroscience, Washington, DC 2003
   Google Scholar
• Wilson GF, Chiu SY. Ion channels in axon and Schwann cell membranes at paranodes of mammalian myelinated fibers studied with patch clamp. J Neurosci 1990a; 10: 3263–3274
   PubMedGoogle Scholar
• Wilson GF, Chiu SY. Potassium channel regulation in Schwann cells during early developmental myelinogenesis. J Neurosci 1990b; 10: 1615–1625
   PubMedGoogle Scholar
• Wu S-X, Koshimizu Y, Feng U-P, Okamoto K, Fujiyama F, Hioki H, Li Y-Q, Kaneko T, Mizuno N. Vesicular glutamate transporter immunoreactivity in the central and peripheral endings of muscle-spindle afferents. Brain Res 2004; 1011: 247–251
   PubMedGoogle Scholar
• Zelená J. The development of Pacinian corpuscles. J Neurocytol 1978; 7: 71–91
   PubMedGoogle Scholar
• Zelená J. The role of innervation in the development and maintenance of mammalian mechanoreceptors. Nerves and mechanoreceptors. Chapman & Hall, New York 1994; 16–17–138–185
   Google Scholar
• Zhang Q, Pangrsic T, Kreft M, Krzan M, Li N, Sul J-Y, Halassa M, Van Bockstaele E, Zorec R, Haydon PG. Fusion-related release of glutamate from astrocytes. J Biol Chem 2004; 279: 12724–12733
   PubMedGoogle Scholar
• Zimmer DB. S100 proteins and S100A1. Celio MR, Pauls T, Schwaller B, Guidebook to the calcium-binding proteins. Oxford University Press, Oxford 1996; 132–137
   Google Scholar