Journal of Shanghai Jiao Tong University (Medical Science) >
Application of three-dimensional electron microscopy to morphological study of neurons in brainstem cochlear nucleus
Received date: 2021-09-07
Online published: 2022-03-17
Supported by
National Natural Science Foundation of China(82171133);Industrial Support Fund of Huangpu District in Shanghai(XK2019011);Shanghai Key Laboratory of Translational Medicine on Ear and Nose Diseases(14DZ2260300)
·To explore the feasibility of cross-scale neuroanatomy and connectomics of mouse cochlear nucleus (CN) by using a new three-dimensional (3D) electron microscopic imaging method.
·The intact CN was obtained after the brain tissue of adult CBA/Ca mice (2 months old) was fixed and dissected, stained with heavy metals (reducing osmium amplification method) , dehydrated with gradient ethanol and anhydrous acetone and embedded with low viscosity resin. The CN tissue was imaged by X-ray microscopy and 3D reconstruction, and its staining quality was evaluated. Then targeted subdivision was located according to the specific distribution of auditory nerve fibers. The low-resolution pre-scan of the CN tissue was performed by scanning electron microscopy, and compared with X-ray microscopic dataset. After the target location was determined, the volume of interest was mapped by serial block-face scanning electron microscopy (SBEM) for 3D reconstruction, and the ultrastructures of bushy cells and the synapses projecting on its surface were tracked, annotated and reconstructed.
·3D electron microscopic samples of intact CN of CBA/Ca mice were successfully prepared. The 3D structure of CN with cell resolution was collected and reconstructed by X-ray microscopic imaging, and the anatomical localization of subregions of CN was achieved. The 3D electron microscopic data of bushy cells in the target area of CN were successfully collected by SBEM. The tracking, labeling and reconstruction of endbulb of Held synapses and other non-auditory synapses on the cell body of target bushy cells were completed. The data of 3D electron microscopy showed that there were 5 endbulb of Held synapses projecting to the surface of the target bushy cell, forming a total of 348 synaptic active zones, while there were 97 synapses from non-auditory nerve.
·It is feasible to prepare 3D electron microscopic samples of adult mouse intact CN by Osmium-based enbloc staining and resin embedding. X-ray microscopic imaging can be used for rapid and accurate localization of subregions and target volume of CN, and the acquired 3D electron microscopic data can be used to study the neuronal morphology and synaptic connections in the CN.
Jialei ZHOU , Haibin SHENG , Haoyu WANG , Yan LU , Fangfang WANG , Hao WU , Yunfeng HUA . Application of three-dimensional electron microscopy to morphological study of neurons in brainstem cochlear nucleus[J]. Journal of Shanghai Jiao Tong University (Medical Science), 2022 , 42(2) : 142 -149 . DOI: 10.3969/j.issn.1674-8115.2022.02.002
1 | OLIVER D L, CANT N B, FAY R R, et al. The mammalian auditory pathways: synaptic organization and microcircuits[M]. Cham: Springer, 2018. |
2 | RYUGO D K, FEKETE D M. Morphology of primary axosomatic endings in the anteroventral cochlear nucleus of the cat: a study of the endbulbs of Held[J]. J Comp Neurol, 1982, 210(3): 239-257. |
3 | ROUILLER E M, CRONIN-SCHREIBER R, FEKETE D M, et al. The central projections of intracellularly labeled auditory nerve fibers in cats: an analysis of terminal morphology[J]. J Comp Neurol, 1986, 249(2): 261-278. |
4 | LIBERMAN M C. Central projections of auditory-nerve fibers of differing spontaneous rate. I. Anteroventral cochlear nucleus[J]. J Comp Neurol, 1991, 313(2): 240-258. |
5 | RYUGO D K, PONGSTAPORN T, HUCHTON D M, et al. Ultrastructural analysis of primary endings in deaf white cats: morphologic alterations in endbulbs of Held[J]. J Comp Neurol, 1997, 385(2): 230-244. |
6 | CAO X J, SHATADAL S, OERTEL D. Voltage-sensitive conductances of bushy cells of the mammalian ventral cochlear nucleus[J]. J Neurophysiol, 2007, 97(6): 3961-3975. |
7 | GóMEZ-NIETO R, RUBIO M E. A bushy cell network in the rat ventral cochlear nucleus[J]. J Comp Neurol, 2009, 516(4): 241-263. |
8 | SPIROU G A, RAGER J, MANIS P B. Convergence of auditory-nerve fiber projections onto globular bushy cells[J]. Neuroscience, 2005, 136(3): 843-863. |
9 | SOTELO C, GENTSCHEV T, ZAMORA A J. Gap junctions in ventral cochlear nucleus of the rat. A possible new example of electrotonic junctions in the mammalian C.N.S[J]. Neuroscience, 1976, 1(1): 5-7. |
10 | WICKESBERG R E, OERTEL D. Tonotopic projection from the dorsal to the anteroventral cochlear nucleus of mice[J]. J Comp Neurol, 1988, 268(3): 389-399. |
11 | OSTAPOFF E M, MOREST D K. Synaptic organization of globular bushy cells in the ventral cochlear nucleus of the cat: a quantitative study[J]. J Comp Neurol, 1991, 314(3): 598-613. |
12 | LAUER A M, CONNELLY C J, GRAHAM H, et al. Morphological characterization of bushy cells and their inputs in the laboratory mouse (Mus musculus) anteroventral cochlear nucleus[J]. PLoS One, 2013, 8(8): e73308. |
13 | NGODUP T, ROMERO G E, TRUSSELL L O. Identification of an inhibitory neuron subtype, the L-stellate cell of the cochlear nucleus[J]. eLife, 2020, 9: e54350. |
14 | LEE D J, CAHILL H B, RYUGO D K. Effects of congenital deafness in the cochlear nuclei of shaker-2 mice: an ultrastructural analysis of synapse morphology in the endbulbs of Held[J]. J Neurocytol, 2003, 32(3): 229-243. |
15 | KIM J J, GROSS J, POTASHNER S J, et al. Fine structure of long-term changes in the cochlear nucleus after acoustic overstimulation: chronic degeneration and new growth of synaptic endings[J]. J Neurosci Res, 2004, 77(6): 817-828. |
16 | LICHTMAN J W, DENK W. The big and the small: challenges of imaging the brain's circuits[J]. Science, 2011, 334(6056): 618-623. |
17 | BRIGGMAN K L, BOCK D D. Volume electron microscopy for neuronal circuit reconstruction[J]. Curr Opin Neurobiol, 2012, 22(1): 154-161. |
18 | TITZE B, GENOUD C. Volume scanning electron microscopy for imaging biological ultrastructure[J]. Biol Cell, 2016, 108(11): 307-323. |
19 | KORNFELD J, DENK W. Progress and remaining challenges in high-throughput volume electron microscopy[J]. Curr Opin Neurobiol, 2018, 50: 261-267. |
20 | HUA Y F, LASERSTEIN P, HELMSTAEDTER M. Large-volume en-bloc staining for electron microscopy-based connectomics[J]. Nat Commun, 2015, 6: 7923. |
21 | GOUR A, BOERGENS K M, HEIKE N, et al. Postnatal connectomic development of inhibition in mouse barrel cortex[J]. Science, 2021, 371(6528): eabb4534. |
22 | HUA Y F, DING X, WANG H Y, et al. Electron microscopic reconstruction of neural circuitry in the cochlea[J]. Cell Rep, 2021, 34(1): 108551. |
23 | WANG H Y, WANG S X, LU Y, et al. Cytoarchitecture and innervation of the mouse cochlear amplifier revealed by large-scale volume electron microscopy[J]. J Comp Neurol, 2021, 529(11): 2958-2969. |
24 | LIU J, WANG S, LU Y, et al. Aligned organization of synapses and mitochondria in auditory hair cells[J]. Neurosci Bull, 2021. DOI: 10.1007/s12264-021-00801-w. |
25 | BOERGENS K M, BERNING M, BOCKLISCH T, et al. webKnossos: efficient online 3D data annotation for connectomics[J]. Nat Methods, 2017, 14(7): 691-694. |
26 | SCHMIDT H, GOUR A, STRAEHLE J, et al. Axonal synapse sorting in medial entorhinal cortex[J]. Nature, 2017, 549(7673): 469-475. |
27 | KARIMI A, ODENTHAL J, DRAWITSCH F, et al. Cell-type specific innervation of cortical pyramidal cells at their apical dendrites[J]. eLife, 2020, 9: e46876. |
28 | MICHANSKI S, SMALUCH K, STEYER A M, et al. Mapping developmental maturation of inner hair cell ribbon synapses in the apical mouse cochlea[J]. Proc Natl Acad Sci U S A, 2019, 116(13): 6415-6424. |
29 | THOMAS C I, KEINE C, OKAYAMA S, et al. Presynaptic mitochondria volume and abundance increase during development of a high-fidelity synapse[J]. J Neurosci, 2019, 39(41): 7994-8012. |
30 | JACKSON D, HOLCOMB P, ELLISMAN M, et al. Two types of somatic spines provide sites for intercellular signaling during calyx of Held growth and maturation[J]. Synapse, 2021, 75(3): e22189. |
31 | BULLEN A, ANDERSON L, BAKAY W, et al. Localized disorganization of the cochlear inner hair cell synaptic region after noise exposure[J]. Biol Open, 2019, 8(1): bio038547. |
32 | NAYAGAM B A, MUNIAK M A, RYUGO D K. The spiral ganglion: connecting the peripheral and central auditory systems[J]. Hear Res, 2011, 278(1/2): 2-20. |
33 | YU W M, GOODRICH L V. Morphological and physiological development of auditory synapses[J]. Hear Res, 2014, 311: 3-16. |
34 | WANG M J, ZHANG C G, LIN S Y, et al. Biased auditory nerve central synaptopathy is associated with age-related hearing loss[J]. J Physiol, 2021, 599(6): 1833-1854. |
35 | WU C, STEFANESCU R A, MARTEL D T, et al. Tinnitus: maladaptive auditory-somatosensory plasticity[J]. Hear Res, 2016, 334: 20-29. |
36 | HEERINGA A N, WU C, CHUNG C, et al. Glutamatergic projections to the cochlear nucleus are redistributed in tinnitus[J]. Neuroscience, 2018, 391: 91-103. |
37 | MANOHAR S, RAMCHANDER P V, SALVI R, et al. Synaptic reorganization response in the cochlear nucleus following intense noise exposure[J]. Neuroscience, 2019, 399: 184-198. |
38 | CONNELLY C J, RYUGO D K, MUNIAK M A. The effect of progressive hearing loss on the morphology of endbulbs of Held and bushy cells[J]. Hear Res, 2017, 343: 14-33. |
39 | DEEP N L, ROLAND J T Jr. Auditory brainstem implantation: candidacy evaluation, operative technique, and outcomes[J]. Otolaryngol Clin North Am, 2020, 53(1): 103-113. |
/
〈 |
|
〉 |