Clin Exp Otorhinolaryngol.  2011 Mar;4(1):18-23.

Decreased Immunoreactivities and Functions of the Chloride Transporters, KCC2 and NKCC1, in the Lateral Superior Olive Neurons of Circling Mice

Affiliations
  • 1Department of Nanobio Medical Science, Dankook University College of Medicine, Cheonan, Korea.
  • 2Department of Anatomy, Dankook University College of Medicine, Cheonan, Korea.
  • 3Department of Physiology, Dankook University College of Medicine, Cheonan, Korea. ansil67@hanmail.net

Abstract


OBJECTIVES
We tested the possibility of differential expression and function of the potassium-chloride (KCC2) and sodium-potassium-2 chloride (NKCC1) co-transporters in the lateral superior olive (LSO) of heterozygous (+/cir) or homozygous (cir/cir) mice.
METHODS
Mice pups aged from postnatal (P) day 9 to 16 were used. Tails from mice were cut for DNA typing. For Immunohistochemical analysis, rabbit polyclonal anti-KCC2 or rabbit polyclonal anti-NKCC1 was used and the density of immunolabelings was evaluated using the NIH image program. For functional analysis, whole cell voltage clamp technique was used in brain stem slices and the changes of reversal potentials were evaluated at various membrane potentials.
RESULTS
Immunohistochemical analysis revealed both KCC2 and NKCC1 immunoreactivities were more prominent in heterozygous (+/cir) than homozygous (cir/cir) mice on P day 16. In P9-P12 heterozygous (+/cir) mice, the reversal potential (Egly) of glycine-induced currents was shifted to a more negative potential by 50 microM bumetanide, a known NKCC1 blocker, and the negatively shifted Egly was restored by additional application of 1 mM furosemide, a KCC2 blocker (-58.9+/-2.6 mV to -66.0+/-1.5 mV [bumetanide], -66.0+/-1.5 mV to -59.8+/-2.8 mV [furosemide+bumetanide], n=11). However, only bumetanide was weakly, but significantly effective (-60.1+/-2.9 mV to -62.7+/-2.6 mV [bumetanide], -62.7+/-2.6 mV to -62.1+/-2.5 mV [furosemide+bumetanide], n=7) in P9-P12 homozygous (cir/cir) mice.
CONCLUSION
The less prominent immunoreactivities and weak or absent responses to bumetanide or furosemide suggest impaired function or delayed development of both transporters in homozygous (cir/cir) mice.

Keyword

Potassium-chloride co-transporter; Sodium-potassium-2 chloride co-transporter; Lateral superior olive; Circling mice

MeSH Terms

Aged
Animals
Brain Stem
Bumetanide
DNA Fingerprinting
Furosemide
Humans
Membranes
Mice
Neurons
Olea
Symporters
Tail
Bumetanide
Furosemide
Symporters

Figure

  • Fig. 1 The reversal potential of the glycine-evoked currents measured from the amplitudes of the responses at different step potentials. Glycine puffs during the voltage steps from -100 mV to -40 mV with increments of 10 mV elicited transient currents (A). In (C), the baseline current at each step potential was subtracted from the raw traces shown in (A). The amplitude of the currents at the vertical dotted line in (C) was plotted as a function of applied potentials (B). Filled circles represent the amplitudes as a function of the command potential, while hollow circles represent the amplitudes as a function of the corrected potential. The corrected potentials (-56, -58, -60, and -63) at given commanding potentials (-40, -50, -60, and -70) are present in (C).

  • Fig. 2 The localization of potassium-chloride co-transporter 2 (KCC2) immunoreactivity (IR) in lateral superior olive (LSO) of heterozygous (+/cir) (A, C) and homozygous (cir/cir) mice (B, D). At P16, KCC2 immunoreactivities were observed in LSO of both genotypes (A, B). The selected areas (dashed-line box) in A and B are magnified in C and D, respectively. The arrows indicate KCC2 immunoreactivity confined to the cell membrane (C, D). Scale bars=200 µm in A, B; 50 µm in C, D.

  • Fig. 3 The localization of sodium-potassium-2 chloride co-transporter 1 (NKCC1) IR in the lateral superior olive (LSO) of heterozygous (+/cir) (A, C) and homozygous (cir/cir) mice (B, D). On P16, NKKC1 immunoreactivities were observed in LSO of both genotypes (A, B). The selected areas (dashed-line box) in A and B are magnified in C and D, respectively. The arrows indicate NKCC1 immunoreactivities (C, D). Scale bars=200 µm in A, B; 50 µm in C, D.

  • Fig. 4 The reversal potential of the glycine-evoked currents at different step potentials. The amplitudes of the currents obtained from P9-P12 heterozygous (Het) (+/cir) or homozygous (Homo) (cir/cir) were plotted as a function of corrected potentials (A, C). The solid lines through the symbols were obtained from a linear fit to the current amplitudes. Filled circles represent the data obtained from control condition, while filled squares and filled triangles present the data from 50 µM bumetanide (Bum) and 50 µM bumetanide plus 1 mM furosemide (Furo), respectively. The means of the Egly with standard errors are presented in (B, D) with bar graphs. The statistical data were obtained from different mice groups (B, Het [+/cir] older than P9; D, Homo [cir/cir] older than P9). *The statistical significance (P<0.05).


Reference

1. Chung WH, Kim KR, Cho YS, Cho DY, Woo JH, Ryoo ZY, et al. Cochlear pathology of the circling mouse: a new mouse model of DFNB6. Acta Otolaryngol. 2007; 3. 127(3):244–251. PMID: 17364360.
Article
2. Lee JW, Lee EJ, Hong SH, Chung WH, Lee HT, Lee TW, et al. Circling mouse: possible animal model for deafness. Comp Med. 2001; 12. 51(6):550–554. PMID: 11924819.
3. Lee JW, Ryoo ZY, Lee EJ, Hong SH, Chung WH, Lee HT, et al. Circling mouse, a spontaneous mutant in the inner ear. Exp Anim. 2002; 4. 51(2):167–171. PMID: 12012726.
Article
4. Gillespie DC, Kim G, Kandler K. Inhibitory synapses in the developing auditory system are glutamatergic. Nat Neurosci. 2005; 3. 8(3):332–338. PMID: 15746915.
Article
5. Hong SH, Kim MJ, Ahn SC. Glutamatergic transmission is sustained at a later period of development of medial nucleus of the trapezoid body-lateral superior olive synapses in circling mice. J Neurosci. 2008; 11. 26. 28(48):13003–13007. PMID: 19036993.
Article
6. Chen G, Trombley PQ, van den Pol AN. Excitatory actions of GABA in developing rat hypothalamic neurones. J Physiol. 1996; 7. 15. 494(Pt 2):451–464. PMID: 8842004.
Article
7. Cherubini E, Rovira C, Gaiarsa JL, Corradetti R, Ben Ari Y. GABA mediated excitation in immature rat CA3 hippocampal neurons. Int J Dev Neurosci. 1990; 8(4):481–490. PMID: 2174638.
Article
8. Luhmann HJ, Prince DA. Postnatal maturation of the GABAergic system in rat neocortex. J Neurophysiol. 1991; 2. 65(2):247–263. PMID: 1673153.
Article
9. Singer JH, Talley EM, Bayliss DA, Berger AJ. Development of glycinergic synaptic transmission to rat brain stem motoneurons. J Neurophysiol. 1998; 11. 80(5):2608–2620. PMID: 9819267.
Article
10. Wu WL, Ziskind-Conhaim L, Sweet MA. Early development of glycine- and GABA-mediated synapses in rat spinal cord. J Neurosci. 1992; 10. 12(10):3935–3945. PMID: 1403091.
Article
11. Kandler K, Friauf E. Development of glycinergic and glutamatergic synaptic transmission in the auditory brainstem of perinatal rats. J Neurosci. 1995; 10. 15(10):6890–6904. PMID: 7472446.
Article
12. Lohrke S, Srinivasan G, Oberhofer M, Doncheva E, Friauf E. Shift from depolarizing to hyperpolarizing glycine action occurs at different perinatal ages in superior olivary complex nuclei. Eur J Neurosci. 2005; 12. 22(11):2708–2722. PMID: 16324105.
13. Plotkin MD, Snyder EY, Hebert SC, Delpire E. Expression of the Na-K-2Cl cotransporter is developmentally regulated in postnatal rat brains: a possible mechanism underlying GABA's excitatory role in immature brain. J Neurobiol. 1997; 11. 20. 33(6):781–795. PMID: 9369151.
Article
14. Rivera C, Voipio J, Payne JA, Ruusuvuori E, Lahtinen H, Lamsa K, et al. The K+/Cl- co-transporter KCC2 renders GABA hyperpolarizing during neuronal maturation. Nature. 1999; 1. 21. 397(6716):251–255. PMID: 9930699.
Article
15. Kitamura A, Ishibashi H, Watanabe M, Takatsuru Y, Brodwick M, Nabekura J. Sustained depolarizing shift of the GABA reversal potential by glutamate receptor activation in hippocampal neurons. Neurosci Res. 2008; 12. 62(4):270–277. PMID: 18840481.
Article
16. Shibata S, Kakazu Y, Okabe A, Fukuda A, Nabekura J. Experience-dependent changes in intracellular Cl- regulation in developing auditory neurons. Neurosci Res. 2004; 2. 48(2):211–220. PMID: 14741396.
Article
17. Fiumelli H, Woodin MA. Role of activity-dependent regulation of neuronal chloride homeostasis in development. Curr Opin Neurobiol. 2007; 2. 17(1):81–86. PMID: 17234400.
Article
18. Vale C, Schoorlemmer J, Sanes DH. Deafness disrupts chloride transporter function and inhibitory synaptic transmission. J Neurosci. 2003; 8. 20. 23(20):7516–7524. PMID: 12930790.
Article
19. DeFazio RA, Keros S, Quick MW, Hablitz JJ. Potassium-coupled chloride cotransport controls intracellular chloride in rat neocortical pyramidal neurons. J Neurosci. 2000; 11. 01. 20(21):8069–8076. PMID: 11050128.
Article
20. Balakrishnan V, Becker M, Lohrke S, Nothwang HG, Guresir E, Friauf E. Expression and function of chloride transporters during development of inhibitory neurotransmission in the auditory brainstem. J Neurosci. 2003; 5. 15. 23(10):4134–4145. PMID: 12764101.
Article
21. Russell JM. Sodium-potassium-chloride cotransport. Physiol Rev. 2000; 1. 80(1):211–276. PMID: 10617769.
Article
22. Payne JA. Functional characterization of the neuronal-specific K-Cl cotransporter: implications for [K+]o regulation. Am J Physiol. 1997; 11. 273(5 Pt 1):C1516–C1525. PMID: 9374636.
23. Bormann J, Hamill OP, Sakmann B. Mechanism of anion permeation through channels gated by glycine and gamma-aminobutyric acid in mouse cultured spinal neurones. J Physiol. 1987; 4. 385:243–286. PMID: 2443667.
Article
24. Backus KH, Deitmer JW, Friauf E. Glycine-activated currents are changed by coincident membrane depolarization in developing rat auditory brainstem neurones. J Physiol. 1998; 3. 15. 507(Pt 3):783–794. PMID: 9508839.
Article
25. Friauf E, Wenz M, Oberhofer M, Nothwang HG, Balakrishnan V, Knipper M, et al. Hypothyroidism impairs chloride homeostasis and onset of inhibitory neurotransmission in developing auditory brainstem and hippocampal neurons. Eur J Neurosci. 2008; 12. 28(12):2371–2380. PMID: 19087168.
Article
26. Kakazu Y, Akaike N, Komiyama S, Nabekura J. Regulation of intracellular chloride by cotransporters in developing lateral superior olive neurons. J Neurosci. 1999; 4. 15. 19(8):2843–2851. PMID: 10191302.
Article
27. de Jong JC, Willems PH, Mooren FJ, van den Heuvel LP, Knoers NV, Bindels RJ. The structural unit of the thiazide-sensitive NaCl cotransporter is a homodimer. J Biol Chem. 2003; 7. 04. 278(27):24302–24307. PMID: 12704198.
Article
28. Moore-Hoon ML, Turner RJ. The structural unit of the secretory Na+-K+-2Cl-cotransporter (NKCC1) is a homodimer. Biochemistry. 2000; 4. 04. 39(13):3718–3724. PMID: 10736171.
29. Blaesse P, Guillemin I, Schindler J, Schweizer M, Delpire E, Khiroug L, et al. Oligomerization of KCC2 correlates with development of inhibitory neurotransmission. J Neurosci. 2006; 10. 11. 26(41):10407–10419. PMID: 17035525.
Article
30. Maric D, Liu QY, Maric I, Chaudry S, Chang YH, Smith SV, et al. GABA expression dominates neuronal lineage progression in the embryonic rat neocortex and facilitates neurite outgrowth via GABA(A) autoreceptor/Cl- channels. J Neurosci. 2001; 4. 01. 21(7):2343–2360. PMID: 11264309.
31. Ben-Ari Y, Khazipov R, Leinekugel X, Caillard O, Gaiarsa JL. GABAA, NMDA and AMPA receptors: a developmentally regulated 'ménage à trois'. Trends Neurosci. 1997; 11. 20(11):523–529. PMID: 9364667.
Article
32. Kirsch J, Betz H. Glycine-receptor activation is required for receptor clustering in spinal neurons. Nature. 1998; 4. 16. 392(6677):717–720. PMID: 9565032.
Article
33. Ben-Ari Y, Tseeb V, Raggozzino D, Khazipov R, Gaiarsa JL. Gamma-Aminobutyric acid (GABA): a fast excitatory transmitter which may regulate the development of hippocampal neurones in early postnatal life. Prog Brain Res. 1994; 102:261–273. PMID: 7800817.
Full Text Links
  • CEO
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr