IL1R2, CCR2, and CXCR4 May Form Heteroreceptor Complexes with NMDAR and D2R: Relevance for Schizophrenia

Abstract

The mild neuroinflammation hypothesis of schizophrenia was introduced by Bechter in 2001. It has been hypothesized that a hypofunction of glutamatergic signaling via N-methyl-D-aspartate receptors (NMDARs) and hyperactivation of dopamine D2 receptors play a role in schizophrenia. The triplet puzzle theory states that sets of triplet amino acid homologies guide two different receptors toward each other and contributes to the formation of a receptor heteromer. It is, therefore, proposed that putative NMDAR-C-C chemokine receptor type 2 (CCR2), NMDAR-C-X-C chemokine receptor type 4 (CXCR4), and NMDAR- interleukin 1 receptor type II (IL1R2) heteromers can be formed in the neuronal networks in mild neuroinflammation due to demonstration of Gly-Leu-Leu (GLL), Val-Ser-Thr (VST), and/or Ser-Val-Ser (SVS) amino acid homologies between these receptor protomers. This molecular process may underlie the ability to produce symptoms of schizophrenia in mild neuroinflammation. In this state, volume transmission (VT) is increased involving increased extracellular vesicle-mediated VT from microglia and astroglia. These vesicles may contain CCR2, CXCR4, and/or IL1R2 as well as their ligands and upon internalization by endocytic pathways into neurons can form heteroreceptor complexes with NMDAR in the plasma membrane with pathological allosteric receptor–receptor interactions involving increased internalization and reduced NMDAR signaling. The triplet puzzle theory also suggests the formation of putative D2R-CCR2, D2R-CXCR4, and D2R-IL1R2 heteromers in mild neuroinflammation in view of their demonstrated sets of Leu-Tyr-Ser (LYS), Leu-Pro-Phe (LPF), and/or Ser-Leu-Ala (SLA) triplet homologies. These D2R heteroreceptor complexes may also contribute to schizophrenia-like symptoms in mild neuroinflammation by enhancing D2R protomer function.

Introduction

The mild neuroinflammation hypothesis of schizophrenia was introduced by Bechter (1–3). Recent work supports a role of inflammation in schizophrenia (4) and a relevant cellular basis appears to be microglia, which upon activation release proinflammatory cytokines (4, 5). It is still unclear, however, if the classical antibiotic drug minocycline can be used as an antipsychotic drug in spite of its ability to block microglia activation. It is known that microglia plays an important role in brain development and possesses protective and destructive functions in neuroinflammation (6–8).

CSF studies may be especially informative on brain events, at least in the clinical situation, and can be performed repeatedly even during acute psychotic episodes. Such studies demonstrated, both in affective and schizophrenic spectrum disorders, the prevalence of activated CSF cells similar to the situation in neurological neuroinflammatory disorders (9, 10). In addition, at least three immunological subgroups were found in affective and schizophrenic spectrum disorders as defined by established CSF examination (11) and a subgroup with increased CSF neopterin (12). In another study, all patients investigated demonstrated an increase of IL8 (13). Taken together, between 70 and 100% of severely diseased patients with the affective and schizophrenic spectrum disorder presented certain CSF abnormalities (14, 15). These findings supported the mild encephalitis (ME) hypothesis of these disorders (1, 2, 16). Further support came from the neurological field with the first description of NMDAR autoimmune encephalitis (17, 18). The more general relevance of the ME hypothesis is suggested by epidemiological findings demonstrating that infections and autoimmune disorders are important risk factors in schizophrenia bipolar and depressive disorders (19–21). Furthermore, recent CSF studies in larger groups of similar psychiatric patient groups also supported this view (22–24).

There is an agreement that the N-methyl-d-aspartate receptor (NMDAR) hypofunction plays an important role in the schizophrenia disease development (25). Previously it was found that chronic brain inflammation can produce a decline in both hippocampal GluN1 NMDARs and GluN2A and GluN2B subunits of NMDARs which likely is mainly caused by reductions in their transcriptional mechanisms (26, 27). They may be linked to cognitive deficits is schizophrenia.

It is, therefore, of high interest that schizophrenia-like symptoms can often be found in patients with NMDAR antibody induced encephalitis (17, 19, 28–30). The NMDAR autoantibodies have been shown to lead to specific, titer-dependent, reversible loss of NMDARs, the dysbalance within the network function being able to explain a spectrum of symptoms (31). It seems possible that the mechanism can involve disturbances in NMDAR function through interactions with the NMDAR antibody leading inter alia to NMDA receptor internalization and breakdown (31). On the other hand, a broad repertoire of antibody-secreting cells is enriched in the CNS during encephalitis producing different types of autoantibodies in parallel in the CSF (32). In addition, for neuronal damage in autoimmune encephalitis cytotoxic, T cells may be responsible not the autoantibodies. Triggers of autoimmune encephalitis may be cancers or virus infections or remain unknown (33). So far, the situation is rather similar to that predicted with the ME hypothesis. The latter is further supported by CSF findings (14, 15) and not least by rare cases of acute psychosis with brain biopsy showing definite but mild neuroinflammation in the cerebral cortex (34–36). Recent evidence for a more general relevance of the ME hypothesis comes also from a postmortem study showing an increased number of immune cells in the brain seemingly linked to a minor blood brain barrier breakdown (37).

Apparently, in classical and ME, one can plausibly expect some general pathological mechanisms but potentially also specific pathological mechanisms to be involved in parallel. There exists no clearcut evidence that specific autoimmunity explains the whole disorder in autoimmune encephalitis (38) nor that it represents an exclusive single pathological mechanism. In multiple sclerosis (MS), there is an early involvement of the cerebral cortex found in both experimental allergic encephalomyelitis (39) and in human MS (40). The interesting findings by Najjar et al. (34–36) in cortical biopsies may similarly represent not only proof for mild local neuroinflammation but may in addition indicate a more distributed mild neuroinflammatory process, the latter indicated by the findings of Bogerts et al. (37).

The current perspective article will discuss the different molecular mechanisms that may underlie the ability of neuroinflammation to produce positive, negative, and/or cognitive symptoms of schizophrenia. It likely involves the release of chemokines and cytokines from activated microglia, astroglia, and monocytes (41, 42), which via volume transmission (VT) can target their receptors on glia and neurons (43, 44). There may also exist an increased extracellular vesicle-mediated VT (44) from glia and megacaryocytes. Glial and immune cells may contain receptor proteins and different forms of mRNAs for chemokine and cytokine receptors in mild neuroinflammation. Extracellular vesicles containing mRNA and proteins for these receptors can via VT communication have a relevant role for producing schizophrenia-like symptoms by being internalized via e.g., cell adhesion receptors into the neuronal component of glia–neuron networks. Extracellular vesicles containing e.g., the cytokine and chemokine receptors may be taken up by an uptake mechanism that depends on proteins located both on the neuronal target cell at extrasynaptic and/or synaptic sites and on the extracellular vesicle (45). The extracellular vesicles are then internalized by a number of endocytic pathways. In this process, the internalized receptors can reach e.g., early endosomes and be rapidly returned to the plasma membrane (46) where they are proposed to interact with extrasynaptic and synaptic NMDARs and D2Rs, indicated to be involved in schizophrenia. This may lead to pathological receptor–receptor interactions in neurons in brain areas with mild neuroinflammation (43, 44).

The allosteric receptor–receptor interactions in D2R heterocomplexes are already indicated to play a role in schizophrenia, especially the antagonistic A2AR–D2R interactions in A2AR–D2R heterocomplexes (47–49). Using the triplet puzzle theory (50), four sets of triplet amino acid homologies were found between the A2AR and D2R protomers which may contribute to the formation of the A2AR–D2R heterocomplexes and to the development of the antagonistic A2A–D2 receptor–receptor interactions (47–49).

Possible Molecular Mechanisms Based on the Triplet Puzzle Theory Contributing to Schizophrenia-Like Symptoms in Mild Neuroinflammation

Triplet Puzzle Theory Supports the Formation of Glutamate NMDAR–CytokineR/ChemokineR Heteroreceptor Complexes through Gly-Leu-Leu (GLL), Val-Ser-Thr (VST), and Ser-Val-Ser (SVS) Homologies

In 2010, based on a bioinformatic approach, it was possible to indicate that receptor that form heterodimers show triplet amino acid homologies (50). This was not observed in pairs of receptors that do not form heterodimers. It was, therefore, proposed that these triplet homologies participate in the receptor interface and gives a code that facilitates the formation of the heterodimer. It was named the triplet puzzle theory (50, 51). The code formed from the triplet amino acid homologies may assist in guiding the receptors toward each other.

Such protriplet homologies appear to be phylogenetically old mechanisms for protein recognition and are already found in integrins (an alpha–beta heterodimer) of marine sponges (52) and remain in human D2 receptor heteromers (53).

It is of particular interest that the NMDAR shows one protriplet amino acid homology with CCR2 (GLL), C-X-C chemokine receptor type 4 (CXCR4) (VST), and interleukin 1 receptor type II (IL1R2) (SVS) (Table 1) as previously observed (43). The GLL protriplet of CCR2 is located in the C-tail and may interact with the GLL of the intracellular part of NR2A (Table 1). The VST protriplet of CXCR4 is also found in the C-tail and may interact with the VST protriplet of the intracellular part of NR2A (Table 1). The VST protriplet of CXCR4 may also interact with the VST in the NR1-1,4,5 subunits present in the C-tail (Table 1). The SVS protriplet is located in the N-terminal of IL1R2 and may interact with the SVS protriplet in the extracellular part of NR2A,B,D (Table 1).

Table 1.

Example of schizo triplets in the interface of human receptor heteromers.

Receptor heteromer	Reference	Ser-Val-Ser (SVS)	Gly-Leu-Leu (GLL)	Val-Ser-Thr (VST)	Leu-Tyr-Ser (LYS)	Leu-Pro-Phe (LPF)	Ser-Leu-Ala (SLA)
GABAB1–GABAB2	(54–56)	−	#	−	−	−	−
GABAB1–CXCR4	(57)	#	−	#	−	−	−
NMDA–CCR2	Possible heteromer	−	#	−	+	−	−
NMDA-interleukin 1 receptor type II (IL1R2)	Possible heteromer	#	−	−	−	−	−
NMDA–CXCR4	Possible heteromer	+	−	#	+	−	−
MOP–DOP	(58)	−	−	−	#	#	−
CCR2–CXCR4	(59)	−	−	−	#	−	−
DOP–CXCR4	(60)	−	−	−	#	#	−
5HT1A–5HT1B	(61)	−	−	−	−	#	#
5HT1A–5HT7	(62)	−	−	−	−	#	#
ADRA2A–ADRA2B	(63)	−	−	−	−	−	#
ADRB2–ADRB3	(64)	−	−	−	−	#	#
D2–CCR2	Possible heteromer	−	−	−	#	−	−
D2–IL1R2	Possible heteromer	−	−	−	−	#	#
D2–CXCR4	Possible heteromer	−	−	−	#	#	−

#, yes in both receptors and may mediate their interaction; +, yes in both receptors; −, no in any receptor.

Location: ec, extracellular; ic, intracellular; TM, transmembrane; SVS—ic GABAB1 # CXCR4; ec NR2A,B,D # IL1R2(N-terminal); GLL—TM GABAB1 # GABAB2; ic NR2A # CCR2(C-tail); VST—ic GABAB1 # CXCR4 (C-tail), NR2A # CXCR4(C-tail), NR1-1,4,5(C-tail) # CXCR4(C-tail); LYS—TM MOP, DOP, CXCR4, D2; LPF—TM MOP, DOP, 5HT1A,B, 5HT7; TM CXCR4 # D2(TM’ec); ec IL1R2 # D2(TM’ec); SLA—TM 5HT1A,B, 5HT7, ADRA2A,B, ADRB2,3; TM IL1R2 # D2. The highlighted text in red color represent the new postulated heteroreceptor complexes based on the Triplet Puzzle Theory

Interleukin 1 receptor type II is a decoy receptor that can bind to IL1α, IL1β, and IL1R antagonist. It can also interact with IL1R accessory protein. It should be noticed that the ITGA-ITGB heterodimer shows a SVS protriplet homology and the GABA B receptor (GABAB1-GABAB2 heterodimer) a GLL protriplet homology and the known GABAB1-CXCR4 heterodimer inter alia a VST and a SVS homology (Table 1). These observations further support the current view that NMDARs can form heterormers with CCR2, CXCR4, and IL1R2.

In mild neuroinflammation, it is proposed that VT is increased involving increased extracellular vesicle-mediated VT from microglia and astroglia (see above). It should, therefore, be considered that these vesicles may contain CCR2, CXCR4, and/or IL1R2, which upon internalization into neurons can form heteroreceptor complexes with NMDAR with pathological allosteric receptor–receptor interactions (Figure 1). If these receptor mechanisms lead to a hypofunction of the NMDAR protomer, they represent one mechanism for the schizophrenia-like effects seen in mild neuroinflammation (3). If the mild neuroinflammation takes place in the hippocampus and the cerebral cortex, the pyramidal nerve cells, key nerve cells in the cortical, and hippocampal circuits will also be affected in view of their expression of NMDA receptors. It will lead to deficits in cognitive functions and contribute to negative symptoms of schizophrenia.

Figure 1.

Illustration of the potential chemokine and cytokine receptor transfer via extracellular vesicle-volume transmission (VT) from immune and microglial cells to striatopallidal GABA neurons [containing dopamine (DA) D2Rs and NMDARs] and hippocampus pyramidal neurons (containing NMDA receptors) in mild inflammation. One mechanism is shown for how chemokine C-X-C chemokine receptor type 4 (CXCR4) and cytokine receptor IL1-R2 including their mRNAs can produce schizophrenia-like symptoms in neuroinflammation. These receptors may be transferred via extracellular vesicle-mediated VT from immune cells, activated microglia, and/or astroglia to nerve cells containing DA D2R and NMDA receptors. Upon internalization, the receptors CXCR4 and IL1-R2 can according to the triplet puzzle theory (see Table 1) form complexes with DA D2R and NMDAR as illustrated here. (A) is shown the D2R-interleukin 1 receptor type II (IL1R2) heteromers in striatopallidal GABA neurons and how they reach the plasma membrane NMDAR via early endosomes and recycling endosomes. (B) is shown the NMDAR-CXCR4 heteromers in the pyramidal nerve cells in the hippocampus with microglial extracellular vesicles containing CXCR4 and also SDF-1alpha reaching the NMDAR in the plasma membrane via internalization and endosomes in the pyramidal cells. Through the development of novel allosteric receptor–receptor interactions in such heteroreceptor complexes, D2R and NMDAR signaling may become pathologically altered contributing to schizophrenia-like symptoms.

These disturbances may become enhanced by an increase in the glia release of the endogenous cytokine and chemokine ligands for these receptors. The agonist induced receptor–receptor interactions can amplify the reduction of NMDAR function in these heterocomplexes and thus help develop the schizophrenia episodes. It will be of high interest to test if the putative NMDAR-CCR2, NMDAR-CXCR4, and NMDAR-IL1R2 heteroreceptor complexes in fact exist using the in situ proximity ligation assay in brain tissue. It is postulated that a reduced NMDAR signaling develop in these heteroreceptor complexes through the agonist activated chemokine and cytokine receptor protomers reducing the NMDAR signaling via allosteric mechanisms in these heterocomplexes. This may also lead to increases in the internalization of these heterocomplexes to late endosomes and lysosomes with a reduction in the density of NMDA receptors. It is unknown if the cytokine and/or chemokine-activated receptor protomer involves a negative allosteric modulation of the glutamate-binding site on GluN2 and/or a negative allosteric modulation of the glycine modulatory site on GluN1 (25).

C-C chemokine receptor type 2 with its ligand CCL2 plays a major role in immunobiology and neurobiology (65). It is mainly located on monocytes and is involved in systemic and brain inflammation. CXCR4 and its ligands CXCL12 are involved in the pathogenesis of brain disease and participate in neuron–glial interactions and in neurotoxicity (66, 67). The IL1R2 exists both in soluble and membrane bound forms, shows no transmembrane signaling, and is regarded as a decoy receptor for IL1 signaling However, it can also act as a binding protein in the membrane and interact with the IL1R accessory protein (68). This accessory protein also exists as an alternatively spliced brain-specific isoform having a significant role in homeostatic sleep (69).

According to the triplet puzzle hypothesis, it can bind to the NMDAR [Table 1; see also Ref. (51)] and form a NMDAR–IL1R2 complex in which NMDAR function is postulated to become reduced. Previous work (70) indicated that this receptor can participate in Alzheimer’s disease, but its biological function is unknown. It may participate in anti-inflammation and help keep the neuroinflammation at a low level.

Triplet Puzzle Theory Supports the Formation of Dopamine (DA) D2R–Cytokine Receptor/Chemokine Receptor Heteroreceptor Complexes through LYS, LPF, and SLA Triplet Homologies

There exists dysregulation of the DA neurons in the pathophysiology of schizophrenia (71). The therapeutic effects of typical and atypical antipsychotic drugs are mainly mediated via blockade of the DA D2 receptors (72, 73) located postjunctionally in the mesolimbic-cortical DA neurons (74–76). The D2Rs are mainly located outside the DA synapses and targeted by extracellular DA VT (76). Over the last decades, the discovery was made that D2Rs participate in many different types heteroreceptor complexes in which D2R protomers directly interact via allosteric mechanisms with other receptor protomers to integrate biological signals changing D2R signaling (47, 49). Some of them offer new targets for the therapeutic effects of D2R antagonists. In other D2R heteroreceptor complexes, the blockade of the D2R protomers by antipsychotic drugs may instead produce side-effects.

It is of particular interest that the NR2B subunit of the NMDAR interacts with the D2R in the glutamate synapses (77), which leads to an antagonistic allosteric receptor–receptor interaction reducing NMDA signaling in the heteroreceptor complex. Thus, DA through VT may diffuse into the glutamate synapses, activate D2R protomers, and reduce NMDAR-mediated synaptic glutamate transmission, which should enhance schizophrenic symptoms according to current hypotheses. The D2Rs and their heteroreceptor complexes are mainly located in the ventral striatopallidal GABA anti-reward neurons. Their enhanced inhibition by enhanced D2R signaling leading to reduced NMDAR signaling should markedly bring down anti-reward activity in this pathway, which can contribute to a malfunction of salience in schizophrenia with all stimuli becoming relevant and disturbing ongoing behavior (49).

It is, therefore, of high interest that, according to the triplet puzzle theory, D2Rs can form heteroreceptor complexes with CCR2, IL1R2, and CXCR4 as indicated for the first time in the current article (Table 1). Three “schizo triplets” were found: LYS, LPF, and SLA. The possible D2R-IL1R2 heterodimer had two sets of triplet homologies, LPF and SLA. LPF is located in the TM6/extracellular region of the D2R and in the extracellular region of the IL1R2 (Table 1). SLA is instead located in TM2 of the D2R and in the TM region of IL1R2 (Table 1). The possible D2R-CXCR4 heterodimer also shows two sets of triplet homologies, one is again LPF, this time located in the interface between TM6-TM2 with the LPF located in the TM2 (Table 1). The other triplet is LYS, which is located in the TM7 of the D2 and in TM3 of the CXCR4 (Table 1) indicating that TM7 and TM3 of the D2R and CXCR4, respectively, can also participate in this interface. The possible D2R-CCR2 heterodimer only exhibits one set of triplet homology that may help mediate the interaction. Also, in this case, the LYS triplet is found and here present in the TM1 of CCR2 that may interact with the LYS triplet in TM7 of D2R.

It is proposed that D2R-CCR2, D2R-IL1R2, and D2R-CXCR4 heteromers can be formed upon mild neuroinflammation in the brain, especially in the ventral striatum. This may contribute to positive schizophrenic symptoms by enhancing D2R inhibitory function in critical brain circuits like the ventral striatopallidal GABA anti-reward pathway leading to exaggerated salience development (Figure 1). Both chemokine and cytokine receptors appear to be involved in forming complexes with the DA D2Rs as is the case with NMDARs. It should also be underlined that the NMDARs interact with the same chemokine and cytokine receptor subtypes as the D2Rs but using different sets of triplet amino acid homologies.

Other GPCR Heteroreceptor Complexes with LYS, LPF, and SLA Homologies

It is of interest that a number of 5HT1A isoreceptor complexes and α2- and β-adrenergic isoreceptor complexes (78) also possess sets of LYS, LPF, and SLA protriplets that may assist in the formation of these isoreceptor complexes (Table 1). Previous work demonstrated also crosstalk between opioid and chemokine receptor subtypes (79) and extensive formation of heteromers take place between opioid and receptor subtypes according to the triplet puzzle theory (80). In Table 1, we report some results from this study showing that LYS and LPF protriplets may also participate in opioid and chemokine isoreceptor complexes as well as in the delta opioid-CXCR4 heterodimer. Their possible role in schizophrenic symptoms in neuroinflammation remains to be explored, but they may have an impact on pain and reward mechanisms (80).

Hypothesis: Glial Cytokine and Chemokine Receptor Subtype Transfer into Neurons in Mild Neuroinflammation Can Produce Novel Dysfunctional NMDAR and D2R Heteroreceptor Complexes Contributing to Schizophrenia Development

This hypothesis is based on the existence of not only soluble VT signals but also of extracellular vesicle-mediated VT signals (44). In 2006, it was found that exosomes can be released from cortical neurons in culture (81). In 2012, cell cultures were demonstrated to transfer GPCRs via extracellular vesicles to other cells and also form GPCR heteromers in the recipient cells by direct interactions with their GPCRs and A2AR-D2R heteromers developed (82). Glial cells, especially the microglia, are activated in inflammation and can release a number of chemokines and cytokines as soluble VT signals and produce a panorama of cytokine and chemokine receptors (6, 83). They may communicate as soluble VT signals (ligands) and via extracellular vesicle-mediated VT as to receptors and their receptor mRNAs (43, 44). The extracellular vesicles may then via cell adhesion receptors become internalized into neurons and their cargo released. In the neurons, CCR2, CXCR4, and IL1R2 can according to the triplet puzzle theory (see above) interact with NMDARs, known to be disturbed in schizophrenia, and as discovered in the current paper with D2Rs, the major target for currently used antipsychotic drugs.

The hypothesis states that the NMDAR protomer develops a hypofunction in mild neuroinflammation due to antagonistic receptor–receptor interactions produced by activation of the CCR2, CXCR4, and/or IL1R2 protomers in the plasma membrane. Their agonist ligands are released by the microglia and/or immune cells and/or astroglia into the extracellular fluid to activate these chemokine and cytokine receptor protomers in the plasma membrane. The current findings based on the triplet puzzle theory indicate that the CCR2, CXCR4, and/or IL1R2 can also interact with D2Rs through such mechanisms. Based on the antipsychotic actions of D2R antagonists, it is proposed that enhancing allosteric receptor–receptor interactions develop in the D2R-CCR2, D2R-CXCR4, and D2R-IL1R2 heteromers upon agonist activation of these chemokine and cytokine receptors leading to increases in D2R protomer signaling with development of schizophrenia-like symptoms.

It will be of high interest to test in cellular models if, in fact, the NMDAR and D2R heteroreceptor complexes with CCR2, CXCR4, and/or IL1R2 protomers are formed using the BRET methodology and the postulated allosteric receptor–receptor interactions develop. We will also test if these NMDAR and D2R heteroreceptor complexes exist in the ventral and dorsal striatum in models of neuroinflammation using the in situ proximity ligation assay and if the proposed allosteric receptor–receptor interactions occur in these brain regions upon neuroinflammation with or without agonist ligands for the CCR2, CXCR4, and/or IL1R2 protomers.

Concluding Remarks

It is proposed that the following mechanisms can contribute to schizophrenia-like symptoms in mild neuroinflammation:

• Extracellular vesicle-mediated VT with receptor and ligand transfer from glial networks to neuronal networks involving distinct cytokine and chemokine receptors and their agonist ligands can lead to formation of dysfunctional and separate NMDAR and D2R heteroreceptor complexes containing CCR2, CXCR4, and/or IL1R2 according to the triplet puzzle theory. The agonist ligands for these three receptors may produce allosteric receptor–receptor interactions in these dysfunctional complexes reducing NMDAR and increasing D2R signaling in the plasma membrane. Schizophrenia-like symptoms may, therefore, develop.

• However, there is no consensus as to which psychopathological symptoms are specific for schizophrenia. There is in fact clear evidence that symptoms in any type of encephalitis are in principle non-specific and variant. As far as the mechanisms proposed in the current paper, they may, from a theoretical perspective, contribute not only to schizophrenia symptoms but may also participate in bipolar disorder and other affective disorders associated with mild neuroinflammation.

• The hypothesis introduced on the formation of distinct NMDAR–cytokine receptor/chemokine receptor and D2R–cytokine receptor/chemokine receptor heterocomplexes with pathological receptor–receptor interactions in the brain upon mild neuroinflammation will primarily be tested as follows: the possible existence of the putative and distinct NMDAR and D2R heteroreceptor complexes will be studied in cellular models and brain models of neuroinflammation using proximity ligation assay and BRET. Then, it will be tested in these models if their allosteric receptor–receptor interactions will lead to a reduction of NMDAR signaling and to increases in D2R signaling in the above heteroreceptor complexes. Finally, if positive results are obtained, the critical role of the demonstrated sets of triplet amino acid homologies for the formation of these heteroreceptor complexes and their receptor–receptor interactions will be tested through mutations of these triplet homologies.

Author Contributions

KF made substantial contributions to the conception and design of the work. He participated in the manuscript writing and critically evaluated it. He agreed with the submission to Frontiers of the current version. DOB-E made substantial contributions to the conception and design of the work, specially the design and conception of the figures. He prepared the reference list and participated in the manuscript writing and critically evaluated it. He agreed with the submission to Frontiers of the current version. AOT made substantial contributions to the conception and design of the work, specially the mathematical and bioinformatic analysis of the amino acid protriplets. He participated in the manuscript writing and critically evaluated it. He agreed with the submission to Frontiers of the current version. KB made substantial contributions to the conception and design of the work. He participated in the manuscript writing and critically evaluated it. He agreed with the submission to Frontiers of the current version.

Conflict of Interest Statement

The authors have no affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. The reviewer MZ and handling Editor declared their shared affiliation, and the handling Editor states that the process nevertheless met the standards of a fair and objective review.

Funding

This work has been supported by grants from the Swedish Medical Research Council (04X-715 and VR-link) to KF, by Hjärnfonden (FO2016-0302) to DOB-E, and by AFA Försäkring (130328) to KF and DOB-E. AOT has not received any support for this work. DOB-E belongs to Academia de Biólogos Cubanos.