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    Topic review

    K+-2Cl− cotransporter 2 (KCC2)

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    Intracellular chloride levels in the brain are regulated primarily through the opposing effects of two cation-chloride co-transporters (CCCs), namely K+-Cl− co-transporter-2 (KCC2) and Na+-K+-Cl− co-transporter-1 (NKCC1). These CCCs are differentially expressed throughout the course of development, thereby determining the excitatory-to-inhibitory γ-aminobutyric acid (GABA) switch. GABAergic excitation (depolarisation) is important in controlling the healthy development of the nervous system; as the brain matures, GABAergic inhibition (hyperpolarisation) prevails. This developmental switch in excitability is important, as uncontrolled regulation of neuronal excitability can have implications for health.

    1. Introduction

    GABA signalling is crucial in both motor and behavioural control; GABAergic neurotransmission is altered in HD [1][2]. To better understand GABAergic activity, we need to consider both K+-2Cl cotransporter 2 (KCC2) expression and the maintenance of neuronal intracellular chloride (Cl) concentration ([Cl]i). Cl is an important anion involved in the regulation of cell volume[3]], proliferation, and apoptosis[4]. Cl has a further role in determining membrane potential and the firing of action potentials[5]. Extracellular [Cl] tends to be fixed, while [Cl]i is more variable[6]. The presence of chloride-cation cotransporters (CCCs) is central to determining [Cl]i[7]. Such transporters are responsible for the bidirectional movement of Cl, and its function is determined by the direction of flux[4].

    GABA is the main inhibitory neurotransmitter in the brain[8]. GABA binds GABA type A receptors (GABAAR); these receptors are ligand-gated anion channels central to the control of Cl movement[8]. Noteworthily, GABAA receptors are permeable for both Cl and bicarbonate (HCO3); the net effect of GABA therefore also depends on the distribution of bicarbonate[9]. Previous studies have also implicated HCO3 in GABAA receptor-mediated depolarization[10][11][12][13][14]. In a recent study, Lombardi et al.[14] suggest that implementation of physiological levels of HCO3-conductivity to GABAA receptors enhances the [Cl]i changes over an extensive range of [Cl]I; however, this outcome strictly depends on the stability of the HCO3 gradient and the intracellular pH. For in-depth understanding on the relationship between distribution of HCO3 and GABA signalling, readers are referred to recent review on the subject[9][15][16][17]. Yet, the reversal potential (when net flow = 0) for GABA (EGABA) is primarily determined by the reversal potential for Cl; GABAergic signalling is therefore dependent on [Cl]i[18]. Whilst inhibitory GABAergic activity is important for proper central nervous system (CNS) functioning[19], GABA can also induce membrane depolarisation[20]. The excitatory action of GABA is important in the development of the nervous system [6]; its roles include regulating synaptogenesis in addition to supporting neurite outgrowth and the maturation of the neuronal network[1][6]. High [Cl]i produces less negative GABA currents that culminate in depolarisation events (excitation)[11]. Conversely, low [Cl]i leads to hyperpolarisation as a result of more negative EGABA values (inhibition) [18]. During development there is a gradual hyperpolarising shift in EGABA as a result of decreased [Cl]i, which is maintained in the mature mammalian brain[22][23]. Since the healthy brain relies on the proper balance between excitatory and inhibitory inputs, uncontrolled regulation of neuronal excitability can have implications for health[3].

    Neuronal [Cl]i is largely regulated through the activity of Na+-K+-2Cl cotransporter 1 (NKCC1) and KCC2 [24][25][26]. NKCC1 pumps Cl into neurons, while KCC2 is responsible for Cl efflux[23][26]. Moreover, the extensively studied CCC family member, NKCC1, has numerous physiological obligations[27][28][29] that make it a promising neurological drug target, owing to its importance in GABAergic signalling[23]. Recently, Chew and colleagues[30] determined the cryo-electron microscopy structure of NKCC1 from Danio rerio. This extensive study revealed the mechanisms involved in NKCC1 molecular transportation and communication and further provided insights into ion selectivity as well as coupling and translocation; a clearer framework for understanding the physiological functions of NKCC1 in relation to human diseases was also established[30]. Besides, modulation of NKCC1 activity alongside that of KCC2 has been implicated in the development and progression of HD[1][31][32][33]. These CCCs are differentially expressed over the course of development, and so the activity of KCC2 and NKCC1 is not synonymous between immature and mature neurons[23]. In the embryonic and early postnatal period, solute carrier family 12 (SLC12), member A1 (SLC12A1) messenger RNA (mRNA) expression of NKCC1 is high[23]. As maturation proceeds, NKCC1 expression decreases and SLC12, member A5 (SLC12A5) expression of mRNA encoding KCC2 is upregulated: there is a resultant net decrease in [Cl]i[23]. The developmental stimulation of KCC2 and inhibition of NKCC1 expression initiates the switch from excitatory to inhibitory GABA signalling [24]. These evolutionarily conserved transporters (KCC2 and NKCC1) are inclusive among central mediators of ion transport in multicellular organisms, with specific roles in regulating ionic and water homeostasis in mammalian CNS[25], which is essential in determining the polarity of the neurons[26]. Notably, during development, [Cl]i increment is prominent in immature neurons and when activated, they display a depolarising response, which is due to the elevated expression of NKCC1 in comparison with KCC2[23]. However, during maturation, NKCC1 expression gradually decreases, and KCC2 expression increases, resulting in an opposite expression pattern[23][36] (also see Figure 2). Importantly, the inhibition/stimulation of KCC2/NKCC1 pair via protein phosphorylation is through a regulatory mechanism that works in a reciprocal pattern[26][37] and members of the with-no-lysine kinase (WNKs) family as well as their downstream targets; STE20/SPS1-related proline/alanine rich kinase (SPAK) and oxidative stress response kinase (OSR1) are the most prominent kinases that regulate this process[25][37][38][39][40]. Consequently, impaired ion homeostasis resulting from mutation in the physiological function of some of this transporter pair and/or their upstream regulators may be detrimental and subsequently result in diminished inhibition and augmented network hyperexcitability, which underlies numerous neurological disorders[25][39][41][42][43][44] including HD[31][32][33].

    Figure 2. GABAA signalling shifts from depolarizing to hyperpolarising responses are mediated by developmental expression of KCC2 and NKCC1 in the brain (neocortical neurons) of rats. The differential expression of these channels regulates intracellular Cl concentration ([Cl]i) and therefore determines the activity of γ-aminobutyric acid (GABA). Na+–K+–Cl cotransporter 1 (NKCC1) pumps Cl into neurons; its expression is high in the early postnatal period, decreasing as maturation proceeds. The expression pattern for K+–2Cl cotransporter 2 (KCC2), responsible for Cl efflux, is directly opposite. In the embryonic and early postnatal periods, [Cl]i is high, and so GABAergic signalling is excitatory (depolarising); as maturation occurs, [Cl]i decreases, initiating the development hyperpolarising shift, whereby GABAergic signalling becomes inhibitory. Figure elements were taken and modified from Tillman and Zhang[26].

    Indeed, loss of KCC2 has implications in disease: KCC2 dysfunction and/or deficiency attenuates Cl efflux and GABAergic inhibition is therefore impaired[5][19]. When [Cl]i exceeds equilibrium, depolarisation events contribute to the onset of neurological disease[8][19]. Decreased KCC2 expression coupled with increased NKCC1 expression and/or activity has been documented in several pathologies[36][41][42][44], including HD[31][32][33]. In HD, HTT is mutated (mHTT) and acts to alter KCC2 and NKCC1 expressions and activity[31][32] through mechanisms that remain undetermined. Since KCC2 and NKCC1 expressions and functionality are crucial in determining the effects of GABA dysregulated KCC2 and NKCC1 activities[3][19][45], subsequent abnormalities in GABAergic signalling are thought to contribute to HD pathogenesis[1]. Hence, this review aims to investigate the possible mechanisms by which KCC2 expression and function is altered in HD. Although HD is primarily characterised by uncoordinated motor activity , patients have additional, co-existing neurological disorders. In view of the aforesaid, the association between altered KCC2 activity, and the comorbidities that present as part of the disease process will also be discussed. For examples, how are NKCC1 and KCC2 expression and activity controlled in the healthy brain? What are the known mechanisms by which KCC2 expression and activity are altered in HD? Additionally, how does altered KCC2 expression and activity contribute to HD comorbidities with a particular focus on cognitive and sleep changes?

    2. KCC2 Regulation and Function in the Healthy Brain

    Phosphorylation Regulation of KCC2 by Protein Kinase Signalling Pathways

    The WNK-SPAK/OSR1 phosphorylate threonine residues 906 and 1007 (T906/T1007) and subsequently downregulate KCC2 mRNA gene expression; thus, a decline in its physiological function is observed[46][47]. The phosphorylation of these residues is highest in the early postnatal period, with a gradual decrease throughout development[46][47]; WNK1 activity is at its most reduced level in mature neurons[37][47]. KCC2-T906/T1007 phosphorylation has been shown to decrease by approximately 95% between embryonic day 18.5 (E18.5) and adulthood in mice[48]. This decrease in threonine phosphorylation may contribute to the developmental onset of KCC2 function[46][47], thereby facilitating the upregulation of Cl extrusion from mature neurons resulting in the hyperpolarising EGABA shift[5][49] (also see Figure 3).

    Figure 3. A novel strategy to facilitate neuronal Cl extrusion and EGABA by coincident NKCC1 inhibition and KCC2 activation by inhibiting the WNK-SPAK/OSR1 kinases. Mammalian neurons that are challenged with multiple neuropsychiatric conditions (such as seizures, neuropathic pain, spasticity, schizophrenia, and others) are usually driven by hyperexcitable circuits, intraneuronal Cl ([Cl]i) levels are elevated due to increased NKCC1 activity, and/or decreased KCC2 activity, promoting GABAAR-mediated membrane depolarization and excitation. In healthy mature neurons, [Cl]i is low due to the opposite activity profile of the CCCs, promoting GABAAR-mediated hyperpolarization, which is critical for the proper balance of excitation–inhibition in neuronal circuits. WNK-SPAK/OSR1 inhibition, via the coincident effects of NKCC1 inhibition and KCC2 activation (the main Cl extrusion mechanism in neurons), might be a potent way of facilitating neuronal Cl extrusion to restore ionic inhibition in diseases that are characterized by disordered Cl homeostasis and GABA disinhibition. ZT-1a, a novel molecular compound, can specifically inhibit SPAK signalling pathway, thus interfering SPAK regulation of GABA signalling via NKCC1 inhibition and KCC2 activation[59]. Activation of protein kinase C (PKC) and brain-type creatine kinase (CKB) are likely to increase KCC2 cell surface expression, but the mechanisms involved are still unclear.

    Moore et al. [49] demonstrated that preventing KCC2-T906/T1007 phosphorylation in vivo (assessed in knock-in mice), via threonine to alanine mutation, accelerates the onset of KCC2 function in the postnatal period. In the study, EGABA values were found to be hyperpolarised across neuronal development (patch-clamp experiment; cultured hippocampal knock-in mouse neurons), i.e., in preventing the phosphorylation of KCC2-T906/T1007, postnatal GABAergic depolarisation activity was largely abolished, thus suggesting that the developmental onset of hyperpolarising synaptic inhibition is dependent on regulated KCC2 phosphorylation[49], and this is further supported by other studies[46][47]. Therefore, potentiating KCC2 function to rescue delayed EGABA shift during development may improve cognitive defects[49]. Serine 940 (S940) is another key phosphorylation site in the regulation of KCC2 activity, phosphorylation of S940 is controlled by protein kinase C (PKC)[50][51]. S940 phosphorylation leads to decreased KCC2 internalisation and subsequent increased Cl extrusion[34], thereby increasing KCC2 function [34][50]. In this regard, Moore et al.[49] further suggest that S940 can be experimentally mutated to alanine (S940A) to prevent its phosphorylation to facilitate [Cl] increment. Briefly, they demonstrated that developmental EGABA shift is delayed in S940A neurons compared to wildtype (WT) controls, thereby suggesting that phospho-regulation of KCC2-S940 may be involved in defining the developmental onset of GABAergic inhibition[49].

    Furthermore, brain-type creatine kinase (CKB) also plays a vital role in regulating cellular energy homeostasis via ATP-dependent phosphorylated catalysis of creatine into phosphocreatine, thereby establishing a readily available ATP-buffering system[52]. Notably, ATP is involved in the activation of Na+-K+-ATPase, which serves as a driving force for KCC activation; hence, it is expected that ATP should enhance the function of KCC2[53]. Interestingly, some reports have affirmed an ATP-induced KCC activation. Aside from potentially providing ATP, Hemmer et al.[54]hypothesize that CKB might phosphorylate KCC2 to change its function, because CKB possesses autophosphorylation activity. However, the implication of the interaction between KCC2 and CKB in relation to their physiological functions and how intracellular ATP concentrations might contribute to KCC2 function is still elusive [53]. More importantly, however, the fact that WNK-SPAK/OSR1 kinase complex is known to phosphorylate and inhibit KCC2 or stimulate NKCC1[25][37][38][39][40] is already established. Thus, molecular compounds that can block WNK-SPAK/OSR1 signalling pathway will result in activating KCC2 and inhibiting NKCC1 activities. The manipulation of the interaction between CKB and KCC2 activities could be a substitute mechanism to achieve KCC2 activation [53][55]. In fact, the interaction between CKB and KCC2 expression/activity has been implicated in the modulation of GABAAR-mediated signalling[1][32]. Furthermore, previous reports have demonstrated that enhancement of CKB activity may facilitate the activation of KCC2 function[55][56][57][58]. In HD, reduced expression and activity of CKB is associated with motor deficits and hearing impairment[56][57]. By and large, the enhancement of CKB activity prior to its interaction with KCC2 activates its function resulting from inhibited phosphorylation of the WNK-SPAK/OSR1 signalling pathway may be a hypothesis worthy of intensive investigations (Figure 3). Hence, it is worthwhile to further investigate the interaction of KCC2 and CKB and how the interaction can modulate the WNK-SPAK/OSR1 signalling cascades in neurological diseases including HD.

    Indeed, phosphorylation status of key regulatory sites on KCC2 determines when the developmental EGABA shift occurs, and regulated depolarising GABAergic signalling (largely in the early postnatal period) is necessary for normal cognitive and behavioural development[49]. Since the phosphorylation process is central to KCC2 function, future research should assess whether the phosphorylation status of key KCC2 sites is constant between HD patients and controls. Further to this, it should be established if phosphorylation status changes as HD progresses. If the phosphorylation of key KCC2 sites does not occur as normal in HD gene carriers and patients, investigating how this affects the development hyperpolarising shift in EGABA is of concern; this research may provide an explanation for the behavioural and cognitive manifestations observed in HD patients. Investigation into the phosphorylation of KCC2 and the EGABA is of increasing interest, especially since it has been suggested that the potentiation of KCC2 function (accelerating hyperpolarising shift) can improve cognitive decline[49].

    This entry is adapted from 10.3390/ijms21239142


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