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BMC Neuroscience

Open Access

NKCC1 downregulation induces hyperpolarizing shift of GABA responsiveness at near term fetal stages in rat cultured dorsal root ganglion neurons

  • Joelle N Chabwine1, 2Email author,
  • Karel Talavera3,
  • Ludo Van Den Bosch4, 5 and
  • Geert Callewaert1
BMC Neuroscience201516:41

https://doi.org/10.1186/s12868-015-0180-4

Received: 19 March 2015

Accepted: 8 July 2015

Published: 14 July 2015

Abstract

Background

GABAA receptor-mediated neurotransmission is greatly influenced by cation-chloride cotransporter activity during developmental stages. In embryonic neurons Na–K–2Cl (NKCC1) cotransporters mediate active chloride uptake, thus increasing the intracellular chloride concentration associated with GABA-induced depolarization. At fetal stages near term, oxytocin-induced NKCC1 downregulation has been implicated in the developmental shift from depolarizing to hyperpolarizing GABA action. Mature dorsal root ganglion neurons (DRGN), however, express high NKCC1 levels and maintain high intracellular chloride levels with consequent GABA-induced depolarization.

Results

Gramicidin-perforated patch-clamp recordings were used to assess the developmental change in chloride homeostasis in rat cultured small DRGN at the embryonic day 16 (E16) and 19 (E19). The results were compared to data previously obtained in fetal DRGN at E14 and in mature cells. A significant NKCC1 downregulation, leading to reduction in excitatory GABAergic transmission, was observed at E16 and E19.

Conclusion

These results indicate that NKCC1 activity transiently decreases in DRGN at fetal stages near term. This developmental shift in GABAergic transmission may contribute to fetal analgesia and neuroprotection at birth.

Keywords

Dorsal root ganglion neuronsGABAIntracellular chlorideNKCC1BumetanideOxytocinFetal analgesia

Background

Cation-chloride cotransporters largely determine the action of GABA during neurogenesis [15]. In immature neurons, Na–K–2Cl (NKCC1) mediates active Cl uptake, promoting depolarizing GABA action, whereas in adult neurons the Cl-extruding KCC2 is generally considered to be involved in generating the hyperpolarizing effect of GABA. Mature dorsal root ganglion neurons (DRGN), however, express high NKCC1 levels and maintain high intracellular Cl concentration ([Cl]i) with resulting GABA-induced depolarization [2, 6, 7]. This property is crucial for presynaptic inhibition of spinal sensory feedback [2, 711].

A NKCC1 downregulation has been observed around birth in different neuronal types of central nervous system (CNS) [2, 12, 13] as a result of circulating maternal oxytocin [1416]. Previously, we showed that DRGN at embryonic day 14 (E14) displayed higher NKCC1 activity and higher intracellular [Cl]i levels than age-matched motor neurons (MN) [17]. Here, we investigated whether DRGN also display NKCC1 downregulation at fetal stages near term, before increasing again to high expression levels in adult stage [18, 19].

Our data show a marked decrease in DRGN [Cl]i at E16 and E19 compared to E14. Decreased activity of NKCC1 at E16 and E19 fully accounts for this reduction in [Cl]i. A possible role for this transient shift in GABAergic responses in DRGN is discussed.

Results and discussion

GABA-induced currents were measured in cultured E16 and E19 DRGN. The results were quantitatively compared to data previously obtained in DRGN at E14 [17].

Total membrane capacitance remained stable between E14 [17] and E16 at 24 ± 2 pF (n = 11, p = 0.43), and slightly increased to 30.7 ± 2 pF at E19 (n = 12, p = 0.006), indicating that most of the cells examined were small DRGN (capacitance 30 ≤ pF) [11]. Based on E GABA , [Cl]i markedly decreased from 44 mM at E14 to 30 and 29 mM at E16 and E19, respectively (Figure 1). In the presence of the selective NKCC1 blocker bumetanide (10 μM), [Cl]i was significantly reduced to ~20 mM at all stages, indicating that NKCC1-dependent Cl influx significantly dropped between E14 (57%) and E16 (33%), with no further decrease up to E19 (38%).
Figure 1

Intracellular [Cl] and bumetanide-induced Cl reduction in DRGN. The resting [Cl]i (open bars) dropped significantly between E14 (44 ± 2 mM, n = 71) and E16 (30 ± 2 mM, n = 11, p = 0.00003), with no further decrease at E19 (29 ± 1 mM, n = 13, p = 0.81). In the presence of 10 μM bumetanide (+Bumet, grey bars), a specific blocker of NKCC1, [Cl]i was decreased to 20 ± 1 mM (n = 6) at E14 and to 18 ± 1 mM (n = 6) at E16 and E19. The bumetanide-insensitive component remained stable at all stages (p = 0.73 for E14 versus E16 and p = 0.46 for E14 versus E19).

Changes in NKCC1 regulation were further explored by studying [Cl]i recovery after Cl load and Cl depletion in DRGN at E19. Applying 1.5 mM GABA for 5 s at a membrane potential of +70 mV consistently shifted the reversal potential in the positive direction, indicating an increase in [Cl]i from 33 to 43 mM (n = 2). Similar results were previously obtained in E14 DRGN [17] (p = 0.38 between respective increases in [Cl]i). Following Cl loading, recovery to basal [Cl]i levels followed a single exponential function with a time constant of 2.97 ± 0.1 min (n = 5, Figure 2b), which is not different from that previously recorded in E14 DRGN [17] (Figure 2a, p = 0.44). Applying 1.5 mM GABA for 5 s at a membrane potential of −100 mV reduced [Cl]i by only 3 mM [from 31 to 28 mM (n = 3)] whereas in E14 DRGN, [Cl]i dropped by 8 mM. This difference in [Cl]i reduction between E14 and E19 DRGN during the depletion protocol was significant (p = 0.009). Following Cl depletion, recovery to the resting [Cl]i level was also significantly slower in E19 DRGN (time constant of 1.64 ± 0.1 min, n = 5) (Figure 2d) than in E14 DRGN (time constant of 0.9 ± 0.1 min) (p = 0.002, Figure 2c). Together, these data strongly suggest that NKCC1-related Cl fluxes markedly decreased in small DRGN after day E14.
Figure 2

Cl load (a, b) and depletion (c, d) in DRGN at fetal stages E14 and E19. DRGN were held at −40 mV and 500 μM GABA was applied for 1 s every 30 s. Cl load was induced by a 5 s GABA pulse (1.5 mM) during a depolarizing step to +70 mV while Cl depletion was induced by applying the same pulse of GABA during a hyperpolarizing step to −100 mV. I GABA was normalized to the value obtained during the voltage step to +70 or −100 mV. The continuous lines show the fit of data during recovery using a single exponential function. Recovery time constants after Cl load were 2.23 and 3.19 min at E14 (a) and E19 (b), respectively. Recovery time constants after Cl depletion amounted to 0.79 and 1.5 min at E14 (c) and E19 (d), respectively. Insets I GABA recordings at times indicated by matched colors.

It was previously shown that mature and embryonic DRGN sustain high [Cl]i owing to high NKCC1 expression [2, 11, 18]. Here, we show that embryonic DRGN undergo a significant downregulation of NKCC1 between E14 and E16 (maintained through E19), which significantly affects Cl homeostasis. The resulting overall decrease in [Cl]i limits the depolarizing action of GABA. Notably, [Cl]i at E14 is comparable to the level reported in the postnatal period (P0–P21) [19, 20] and possibly in adult DRGN [18] implying that the observed drop in [Cl]i between day E16 and E19 is only a transient phenomenon. The underlying mechanism most probably involves decreased NKCC1 activity rather than lower expression level [14, 2022].

Conclusion

These data accord with previous observations in other CNS neuronal types showing that NKCC1 activity is decreased as a result of increasing levels of circulating maternal oxytocin at near term. However, in contrast to other neuronal types, the activity-dependent downregulation of NKCC1 in DRGN is not permanent but only transient. Since we predominantly studied small DRGN (capacitances ≤30 pF) [11] in which GABA-induced depolarization is essential for sensory perception [2, 79, 11], we suggest that the transient GABAergic hyperpolarizing shift observed between E16 and E19 reflects oxytocin-induced fetal adaptation to delivery [14, 16], contributes to fetal analgesia and protects the fetus against neuronal insult.

Methods

All experimental procedures were approved by the local Ethical Committee and were therefore performed in accordance with international ethical regulations. DRGN were derived from Wistar rat embryos at E16 and E19, and cultured as previously described [17]. Tissue samples were trypsinized and triturated and neurons were purified by centrifugation using a bovine serum albumin cushion and then plated on poly-l-ornithine and laminin-coated glass coverslips. Neurons were used between 3 and 6 days after plating. GABA-induced currents (I GABA ) were recorded under voltage-clamp conditions using gramicidin-perforated patches [17] (75 μg/ml, Fluka). The pipette solution contained (in mM): CsCl 125, MgCl2 1.2, HEPES 10, Na2ATP 2 and EGTA 1 and the pH was adjusted to 7.3 with CsOH. Patch pipettes (3–5 MΩ resistance) were briefly dipped in gramicidin-free pipette solution and back-filled with internal solution. After seal formation and stable access resistance ≤30 MΩ, GABA was locally applied using a fast perfusion system. The external solution contained (in mM): NaCl 150, KCl 6, MgCl2 1, CaCl2 3, HEPES 10 and glucose 10, pH adjusted to 7.3 with NaOH. 500 nM TTX (tetrodotoxin, Alomone labs) and 100 μM Cd2+ were added to block voltage-gated Na+ and Ca2+ channels, respectively. Total external [Cl] amounted to 164 mM. Bumetanide (10 μM) was used to specifically block NKCC1 cotransporters [4, 6].

The reversal potential for I GABA , (E GABA ) determined with brief voltage ramps during GABA application, was used to estimate intracellular Cl levels [17]. Intracellular [Cl] depletion or loading was achieved by applying a 5 s pulse of GABA (1.5 mM) during a voltage step from the holding potential (−40 mV) to −100 mV or to +70 mV, respectively [12]. After depletion or loading, [Cl] recovery was monitored by applying successive 1 s-GABA pulses of 500 μM every 30 s. [17]. All data are shown as mean ± SEM. Statistically significant differences were evaluated with unpaired Student t test (p < 0.05).

Abbreviations

[Cl]i

intracellular chloride concentration

CNS: 

central nervous system

DRGN: 

dorsal root ganglion neuron

E GABA

reversal potential for I GABA

EGTA: 

ethylene glycol tetraacetic acid

E14: 

embryonic day 14

E16: 

embryonic day 16

E19: 

embryonic day 19

GABA: 

gamma amino butyric acid

HEPES: 

4-(2-Hydroxyethyl)piperazine-1-ethanesulfonic acid

I GABA

GABA-induced current

KCC2: 

potassium–chloride (K–Cl) cotransporter 2

MN: 

motor neuron

NKCC1: 

sodium–potassium–chloride (Na–K–2Cl) cotransporter 1

P0: 

post-natal day 0

P21: 

post-natal day 21

TTX: 

tetrodotoxin

Declarations

Authors’ contributions

JNC designed the study, carried all experiments, analyzed data, drafted and revised the manuscript. KT significantly contributed to the conception and the design of the study, to data analysis and to the revision of the manuscript. LVDB contributed to data acquisition, data analysis and manuscript revision. GC supervised the whole study, significantly contributed to its conception and experimental design, to data acquisition and analysis, and to manuscript revision. All authors read and approved the final manuscript.

Acknowledgements

Research was funded by the European Research Council under the European’s Seventh Framework Programme (FP7/2007-2013)/ ERC Grant agreement no 340429, by the Interuniversity Attraction Poles Programme P7/16 initiated by the Belgian Science Policy Office and by the Research Council of the KU Leuven (EF/95/010 and PF-TRPLe).

Compliance with ethical guidelines

Competing interests The authors declare that they have no competing interests.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Department of Cellular and Molecular Medicine, Katholieke Universiteit Leuven (KU Leuven), Louvain, Belgium
(2)
Neurology Unit, Department of Medicine, Faculty of Sciences, University of Fribourg, Fribourg, Switzerland
(3)
Laboratory of Ion Channel Research and TRP Channel Research Platform (TRPLe), Department of Cellular and Molecular Medicine, KU Leuven, Louvain, Belgium
(4)
Laboratory of Neurobiology, Experimental Neurology and Leuven Research Institute for Neuroscience and Disease (LIND), KU Leuven, Louvain, Belgium
(5)
VIB, Vesalius Research Center, KU Leuven, Louvain, Belgium

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Copyright

© Chabwine et al. 2015

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