Oligodendrocyte Precursor Cells Synthesize Neuromodulatory Factors

NG2 protein-expressing oligodendrocyte progenitor cells (OPC) are a persisting and major glial cell population in the adult mammalian brain. Direct synaptic innervation of OPC by neurons throughout the brain together with their ability to sense neuronal network activity raises the question of additional physiological roles of OPC, supplementary to generating myelinating oligodendrocytes. In this study we investigated whether OPC express neuromodulatory factors, typically synthesized by other CNS cell types. Our results show that OPC express two well-characterized neuromodulatory proteins: Prostaglandin D2 synthase (PTGDS) and neuronal Pentraxin 2 (Nptx2/Narp). Expression levels of the enzyme PTGDS are influenced in cultured OPC by the NG2 intracellular region which can be released by cleavage and localizes to glial nuclei upon transfection. Furthermore PTGDS mRNA levels are reduced in OPC from NG2-KO mouse brain compared to WT cells after isolation by cell sorting and direct analysis. These results show that OPC can contribute to the expression of these proteins within the CNS and suggest PTGDS expression as a downstream target of NG2 signaling

Daily Eastern News: March 03, 2017

https://thekeep.eiu.edu/den_2017_mar/1002/thumbnail.jp

Die Rolle der Oligodendrozyten-Vorläuferzellen im Zentralen Nervensystem

Im Fokus dieser Studie stehen die zu den Gliazellen zählenden OPC, sowie das von diesen exprimierte Typ-1 Membranprotein NG2. Dieses wird auf eine Prozessierung durch α- und γ-Sekretase, in Analogie zu Proteinen wie Notch oder APP, untersucht.rnEine solche Prozessierung ginge mit zusätzlichen intrazellulären Spaltprodukten neben der bekannten Ektodomäne einher. Da OPC mit dem Neuronalen Netzwerk durch synaptische Innervierungen in Verbindung stehen, stellt sich die Frage, ob diese mit der Spaltung von NG2 in Verbindung gebracht werden können. Dazu käme mechanistisch beispielsweise eine aktivitätsabhängige Regulierung der Proteolyse, wie sie jüngst für das neuronale synaptische cell adhesion molecule Neuroligin gezeigt werden konnte, in Frage. Zudem werden eine physiologische Rolle der NG2 Ektodomäne bzw. der möglichen intrazellulären Fragmente untersuchen. Insbesondere potentielle neuromodulatorische Funktionen sind hier von Interesse, da diese die OPC tiefer in das Neuronale Netzwerk integrieren würden. Die Existenz eines NG2 Homologes in D. melanogaster, wirft weiterhin die Frage auf, in wie weit diese Mechanismen in diesem Modellsystem konserviert sind.rnIn Analogie zur Lokalisierung von Markerproteinen an Neuron-Neuron Synapsen in vivo, ergibt sich die Frage ob sich die synaptischen Verbindungen zwischen Neuronen und OPC in ähnlicher Weise darstellen lassen.rnEin Charakteristikum von OPC ist die Teilungsaktivität in sich entwickelnden und adulten Säugern. Zudem gibt es Evidenzen für direkte funktionelle Verknüpfungen zwischen dem NG2 Protein und dem Teilungsmodus der OPC. Deshalb war ein weiteres Ziel mögliche Änderungen in der Zellteilung der OPC, die mit dem NG2 Protein in Verbindung stehen könnten, in NG2 -/- Mäusen zu untersuchen.rnThe main focus of this thesis is given to a subtype of glia cells so called oligodenderocyte precursor cells or short OPC and the type-1 membrane protein NG2 which is expressed by these OPC within the CNS. Thereby proteolytic processing by α- and γ-secretases of NG2 is investigated like it has been established for the Notch and APP protein.rnSuch proteolytic processing would go along with the creation of intracellular cleavage products which are additional to the cleaved known ectodomain of NG2. Since OPC receive direct synaptic input from the neuronal network, it is conceivable that the cleavage of NG2 could be connected to this innervation. This could be a similar mechanism as it has recently been shown for the synaptic cell adhesion molecule Neuroligin, whose cleavage has been shown to be dependent on neuronal activity. Therefore a physiological role for the NG2 ectodomain and the potential intracellular cleavage fragments could be of great importance. Especially neuromodulatroy functions are of interest here, as they would integrate OPC deeper into the neuronal network. Since NG2 has a conserved homologue in D. melanogaster, it is most relevant if these potential mechanisms are conserved as well.rnStainings of synaptic marker proteins are suitable to identify neuron-neuron synapse in vivo. Thus synaptic connections between Neuron-OPC are likely to be described in a similar fashion. rnOne characteristic feature of OPC is their ability to proliferate during development and in adulthood. There are furthermore evidences between NG2 expression and proliferation behavior of OPC. Hence it was one goal to investigate differences in proliferation of OPC within the NG2 knock-out mouse.r

The role of the NG2 proteoglycan in OPC and CNS network function

In the normal mammalian CNS, the NG2 proteoglycan is expressed by oligodendrocyte precursor cells (OPC) but not by any other neural cell-type. NG2 is a type-1 membrane protein, exerting multiple roles in the CNS including intracellular signaling within the OPC, with effects on migration, cytoskeleton interaction and target gene regulation. It has been recently shown that the extracellular region of NG2, in addition to an adhesive function, acts as a soluble ECM component with the capacity to alter defined neuronal network properties. This region of NG2 is thus endowed with neuromodulatory properties. In order to generate biologically active fragments yielding these properties, the sequential cleavage of the NG2 protein by α- and γ-secretases occurs. The basal level of constitutive cleavage is stimulated by neuronal network activity. This processing leads to 4 major NG2 fragments which all have been associated with distinct biological functions. Here we summarize these functions, focusing on recent discoveries and their implications for the CNS. This article is part of a Special Issue entitled SI:NG2-glia(Invited only)

NG2 intracellular fragments influence PTGDS protein levels.

<p><b>A</b> Expression of NG2_del, NG2_ICD (both red) and Mock (empty Plasmid) constructs in the OPC cell-line Oli-neu, resulted in a reduction of PTGDS protein levels in post nuclear lysates (PN). Overexpression of these constructs leads to a changed ratio of protein levels between the NG2 FL and the small NG2 (intracellular) cleavage fragments the CTF and the ICD (compare to mock, see B). <b>B</b> Cartoon of NG2, NG2 expression constructs (red) and the cleavage sites for α- and γ-secretase leading to the creation of the CTF (12 kD) and ICD (8.5 kD, both blue). (A: 4 independent transfections were analyzed per construct; two tailed student’s t-test was performed.)</p

The NG2 ICD is located in the nucleus.

<p><b>A</b> Cartoon of the NG2 full length protein and the major cleavage fragments (ectodomain, CTF, ICD). Ectodomain cleavage (indicated by the α) has been reported by others [<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0127222#pone.0127222.ref028" target="_blank">28</a>], while intracellular cleavage (indicated by the γ) has been found by our group [<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0127222#pone.0127222.ref021" target="_blank">21</a>]. Expression constructs NG2_del leading to high NG2 CTF and lower ICD levels by proteolytic processing and the NG2_ICD construct leading to high levels of NG2 ICD are both shown in red. <b>B</b> Cytoplasmic (cyto), crude membrane (CM) and nuclear fractions of HEK cells transfected with empty plasmid (control), NG2_ICD, or NG2_del are shown. NG2_del full-length (FL) protein, the membrane bound NG2 CTF and the NG2 ICD are shown in WB (schematically shown in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0127222#pone.0127222.g002" target="_blank">Fig 2D</a>). The NG2 ICD shows the highest levels when expressed as a recombinant protein (NG2_ICD). This is present in all fractions but highest in the nuclear fraction. NG2_del-derived NG2 ICD (generated by proteolysis) is only detectable in the nuclear fraction and runs at the same size as the recombinant NG2 ICD.</p

NG2 dependent regulation of PTGDS and Nptx2 <i>in vivo</i>.

<p><b>A&B</b> mRNA levels of target-genes were directly analyzed by qRT-PCR from FACS isolated OPC and other cells (negative (neg.) sort). Single cell suspensions from total brains of postnatal day 9 (P9) NG2-KO and WT mice were used for FACS. <b>A</b> Enrichment of target mRNA in OPC in comparison to other cell-types is shown for WT (black bar) and NG2-KO (grey bar), (ΔΔCT = [ΔCT OPC]–[ΔCT other cells]). Enrichment of PDGFRα mRNA validates OPC enrichment. Nptx2 mRNA was enriched within OPC of both genotypes, while PTGDS mRNA was only enriched in WT OPC. <b>B</b> Genotype-specific mRNA enrichment in OPC (black bar) and other cells (grey bar) is plotted (ΔΔCT = [ΔCT WT cells]–[ΔCT KO cells]). PTGDS was the sole target gene analyzed exhibiting differential expression between WT and KO genotypes. Expression was highly increased in WT-derived OPC and down-regulated in the other cells (neg. sort) from these mice. <b>C</b> Western Blot of soluble protein fractions. Soluble fractions were extracted from P9 mouse brain of WT and NG2-KO mice. Total PTGDS and Nptx2 protein levels show no difference between genotypes. <b>D</b> Protein levels of post nuclear (PN) cell lysates of the OPC cell line Oli-neu were analyzed after treatment with siRNA silencing NG2 expression (siNG2) or control siRNA (siC). Full-length NG2 levels were reduced as well as PTGDS protein levels, fitting to the reduced mRNA levels of PTGDS found in NG2-KO OPC (B). <b>E</b> Expression of PTGDS mRNA by the OPC cell-line Oli-neu as revealed by <i>in situ</i> hybridization. (A&B: for NG2-KO OPC, 4 independent sorts were analyzed, for WT 3 sorts were analyzed, ΔCT = (CT target)–(CT GAPDH), ΔCT and ΔΔCT values are in log2 scale; for <b>C:</b> 4 animals were analyzed for NG2-KO (KO1-4) and BL6/N (WT1-4) mice; for <b>D</b>: 4 independent transfections were analyzed per siRNA, two tailed student´s t-test was performed.)</p

Expression of PTGDS and Nptx2 in primary OPC.

<p><b>A</b> Expression of cell-type specific markers was analyzed by Western-Blot of total cell lysates of pOPC and the negative (neg.) sort fractions, HEK cells and primary cortical neurons (DIV5 in culture). <b>B-D</b> show the expression of proteins in pOPC over time, related to DIV0. In <b>B</b> a peak of the OPC protein NG2 is shown at DIV1, PLP indicates differentiation into oligodendrocytes starting at DIV2, GFAP shows astrocyte differentiation starting at DIV2. <b>C</b> PTGDS expression peaks together with NG2 at DIV1. <b>D</b> Nptx2 expression increases together with NG2 at DIV1, peaks at DIV2 and returns to basal levels at DIV4. <b>E</b> Expression of PTGDS and Nptx2 mRNA in pOPC at DIV1, as revealed by <i>in situ</i> hybridization, OPC were identified by antibody staining of NG2 protein. (A-D: 3 sorts were analyzed for each time point. Two tailed student’s t-test was applied.)</p

Oligodendrocyte Precursor Cells Modulate the Neuronal Network by Activity-Dependent Ectodomain Cleavage of Glial NG2

<div><p>The role of glia in modulating neuronal network activity is an important question. Oligodendrocyte precursor cells (OPC) characteristically express the transmembrane proteoglycan nerve-glia antigen 2 (NG2) and are unique glial cells receiving synaptic input from neurons. The development of NG2+ OPC into myelinating oligodendrocytes has been well studied, yet the retention of a large population of synapse-bearing OPC in the adult brain poses the question as to additional functional roles of OPC in the neuronal network. Here we report that activity-dependent processing of NG2 by OPC-expressed secretases functionally regulates the neuronal network. NG2 cleavage by the α-secretase ADAM10 yields an ectodomain present in the extracellular matrix and a C-terminal fragment that is subsequently further processed by the γ-secretase to release an intracellular domain. ADAM10-dependent NG2 ectodomain cleavage and release (shedding) in acute brain slices or isolated OPC is increased by distinct activity-increasing stimuli. Lack of NG2 expression in OPC (NG2-knockout mice), or pharmacological inhibition of NG2 ectodomain shedding in wild-type OPC, results in a striking reduction of N-methyl-D-aspartate (NMDA) receptor-dependent long-term potentiation (LTP) in pyramidal neurons of the somatosensory cortex and alterations in the subunit composition of their α-amino-3-hydroxy-5-methyl-4-isoxazolepr opionicacid (AMPA) receptors. In NG2-knockout mice these neurons exhibit diminished AMPA and NMDA receptor-dependent current amplitudes; strikingly AMPA receptor currents can be rescued by application of conserved LNS protein domains of the NG2 ectodomain. Furthermore, NG2-knockout mice exhibit altered behavior in tests measuring sensorimotor function. These results demonstrate for the first time a bidirectional cross-talk between OPC and the surrounding neuronal network and demonstrate a novel physiological role for OPC in regulating information processing at neuronal synapses.</p></div