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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
 
J Neurosci. Author manuscript; available in PMC 2010 December 1.
Published in final edited form as:
PMCID: PMC2927324
NIHMSID: NIHMS213320

BMP9 induces NGF as an autocrine/paracrine cholinergic trophic factor in developing basal forebrain neurons

Abstract

Acetylcholine (ACh) synthesis and release from basal forebrain cholinergic neurons (BFCN) innervating the cerebral cortex and hippocampus are essential processes for normal learning, memory and attention. Bone morphogenetic protein (BMP) 9 is a cholinergic differentiation factor in the developing septum that increases ACh synthesis and choline acetyltransferase (Chat) gene expression both in vivo and in vitro. We investigated the possible induction of cholinergic trophic factors by BMP9 in murine septal cells. Nerve growth factor (NGF) protein expression and secretion into the medium was increased in cultured embryonic septal cells treated with BMP9, and partially mediated BMP9-induced acetylcholine production and Chat gene expression. BMP9-induced Ngf gene expression was detected in post-mitotic cells, required new protein synthesis and was blocked by BMP type I receptor inhibition. Cholinergic neurons were isolated by fluorescence-activated cell sorting based on either transgenic expression of green fluorescent protein driven by the Chat promoter or NGF receptor (p75) immunostaining. Although both non-cholinergic and cholinergic neurons in untreated cultures expressed similar low levels of Ngf, increased Ngf gene expression was restricted to Chat-positive neurons in BMP9 treated cultures. Likewise, similar levels of Ngf mRNA were detected in p75-negative and p75-postive septal cells, yet only p75-positive BFCN increased their Ngf gene expression when treated with BMP9, and only these cells expressed the Alk1 BMP receptor. The data suggest an autocrine/paracine role for NGF in the development and/or maintenance of BFCN and imply that the stimulation of NGF production and release contributes to the cholinergic-supportive properties of BMP9.

Keywords: Basal forebrain, Cholinergic neuron, Septum, Nerve growth factor, Neurotrophin, Differentiation, Fluorescence

Introduction

Basal forebrain cholinergic neurons (BFCN) project to the hippocampus and cerebral cortex where the release of their neurotransmitter, acetylcholine (ACh), is central for the processes of attention, learning and memory throughout life. During development, cholinergic innervation is necessary for the proper morphogenesis of target regions, and its early modulation has a lasting impact on adult behaviors (Leanza et al., 1996; Ricceri et al., 2002). Moreover, decline in BFCN function and cholinergic marker expression is apparent in Alzheimer's disease (AD) patients (Mufson et al., 2008), in aged animals and in genetic animal models of AD (Koh et al., 1989; Greferath et al., 2000; Cassel et al., 2008). Treatments for AD have focused on increasing cholinergic tone by inhibiting acetylcholinesterase. More recently, administration of trophic factors that support the function and survival cholinergic neurons has been explored (Tuszynski et al., 2005).

Neurotrophic factors are required for the development, maintenance and neuroprotection of BFCN. Nerve growth factor (NGF) in particular supports multiple aspects of cholinergic development and differentiation, including increasing the number and soma size of choline acetyltransferase (ChAT)-positive neurons and promoting neurite outgrowth and ChAT activity in neonatal septum, hippocampus and neocortex (Mobley et al., 1986; Hartikka and Hefti, 1988a; Sofroniew et al., 2001). Neonatal intraventricular administration of NGF increases the expression of Chat and Ntrk1, the gene that encodes the high-affinity NGF receptor TrkA, whereas administration of anti-NGF decreases the expression of both genes (Li et al., 1995). Though the primary source of NGF to BFCN is likely retrograde transport from target areas, predominantly the cortex and hippocampus (Sofroniew et al., 2001), NGF is also produced locally in the septum (Large et al., 1986; Saporito and Carswell, 1995). This source of NGF may be especially important during development of BFCN before they reach innervation targets.

Bone morphogenetic proteins (BMPs) play critical roles in central nervous system patterning, predominantly during early development (Liu and Niswander, 2005). BMPs bind to type I and type II TGFβ family receptors that primarily transduce signals via the Smad pathway (Liu and Niswander, 2005). BMP9 in particular is a cholinergic differentiation factor for BFCN. Application of BMP9 to both septal cell cultures and into the cerebral ventricles of developing mouse embryos significantly increases ACh production (Lopez-Coviella et al., 2000). In various in vitro models BMP9 increases the expression of BFCN markers, in particular ChAT and, interestingly the low affinity NGF receptor (p75) (Lopez-Coviella et al., 2000; Lopez-Coviella et al., 2005; Schnitzler et al., 2008a). Because prolonged exposure (days) to BMP9 is required to achieve its' full effects on Chat expression and ACh production, we hypothesized that BMP9 may – at least in part – function by modulating the neurotrophic factor environment in favor of cholinergic development and maintenance. The data presented herein are consistent with this hypothesis.

Materials and Methods

Timed-pregnant CD-1 mice were obtained from Charles River Laboratories (Wilmington MA). Chat-eGFP mice, which express a bacterial artificial chromosome transgene containing eGFP at the ChAT start site, were generated as previously described (Tallini et al., 2006). Recombinant human BMP9 was a gift from Wyeth Research. All reagents and chemicals were obtained from Sigma-Aldrich (St. Louis MO), unless otherwise noted.

Septal cell isolation and culture

E14-18 septa were dissected and dissociated as previously described (Schnitzler et al., 2008b, a). Cells were plated at a density of 1.25 × 105 cells per cm2 on poly-D-lysine / laminin-coated tissue culture-ware in 10 % FBS / DMEM supplemented 20 ng/mL bFGF (PeproTech, Rocky Hill NJ), 50 U/mL penicillin and 50 μg/mL streptomycin (pen/strep; Invitrogen), and cultured at 37°C in 5% CO2. Sixteen hours after plating, culture medium was changed to Neurobasal medium (NB, Invitrogen) containing 2% B-27 (Invitrogen) supplement, 250 μM L-glutamine, 250 μM GlutaMax (Invitrogen), pen/strep, 20 ng/mL bFGF and 2 μM cytosine arabinoside hydrochloride (AraC), unless otherwise noted. Cells were treated every 24 hours or as indicated with BMP9, cycloheximide, Compound C, TrkA inhibitor (#648450, Calbiochem, Gibbstown NJ), or anti-NGF antibody (Millipore, Bedford MA, clone 27/21). Half the volume of media was exchanged every 48 hours. Cultured cells to be analyzed by FACS were rinsed with PBS and trypsinized for 5 minutes at 37°C. Cells were then briefly triturated through fire-polished, siliconized glass pipets in 1:2:4 v/v 4% BSA in PBS:10% FBS in DMEM:Hibernate E medium containing 100 U/mL DNAse. Finally, the cells were centrifuged through a 4% BSA / PBS cushion, and immunostained as described below.

Fluorescent-activated cell sorting (FACS)

E18 septal cells were sorted as previously described (Schnitzler et al., 2008b). Briefly, cells were stained at a concentration of 20 × 106 cells per mL in 0.2% BSA/Hibernate E medium with 5 μg/mL anti-p75 affinity-purified antibody (ATS, San Diego CA) for 35 min at 4°C. Cells were washed with 0.2% BSA, and incubated with an Alexa 488-conjugated anti-rabbit-IgG secondary antibody (Molecular Probes, 1:500) for 25 minutes at 4°C. Cells were washed, and resuspended in 0.2% BSA in Hibernate E medium prior to sorting on a MoFlo cell sorter (DakoCytomation, Denmark). Cells were collected into 20% FBS / Hibernate E medium. Data were acquired and analyzed using Summit software (DakoCytomation). All FACS dot plot x- and y- axes indicate fluorescence intensity.

Reverse transcriptase PCR

RNA for RT-PCR was isolated using an RNAqueous-micro kit according to the manufacturer's instructions (Ambion, Austin TX). RNA was quantified using the RiboGreen reagent (Molecular Probes, Carlsbad CA). RT-PCR was performed using the SuperScript One-Step with Platinum Taq kit (Invitrogen). Each reaction included 1.2 – 2.2 mM MgSO4 and 10 – 50 ng of RNA. Reaction conditions were optimized for each primer set (see Figure S1 for primer sequences) such that product amplification fell within the linear range of both cycle number and RNA concentration. The RT-PCR reaction products were electrophoresed through 1.8% agarose or 10% acrylamide gels at 100 V, visualized with ethidium bromide on an ImageStation 440CF (Kodak, Rochester NY) and analyzed with Kodak 1D Image Analysis software.

Immunoblotting

Cells were lysed in buffer containing 50 mM Tris pH 7.5, 150 mM NaCl, 1% NP-40, 0.2% SDS, 0.5% deoxycholic acid, 1 mM Na3VO4, 25 mM NaF and 1% protease inhibitor cocktail (#P8340, Sigma). Equal amounts (4-10 μg) of each sample was electrophoresed through 10% Bis-Tris pre-cast gels (Invitrogen) and transferred to blotting membrane using the iBlot system (Invitrogen). Membranes were blocked with 4% milk in PBS / 0.1% Tween (PBS-T), washed with PBS-T and probed with anti-phospho-SMAD1/5/8 (1:1000, Santa Cruz) or anti-β-actin (1:2000) followed by species-specific anti-IgG-HRP (1:5000, BioRad). Reactive bands were detected with SuperSignal West Femto chemiluminescent substrate (Pierce, Rockford IL), captured with an ImageStation 440CF and their intensities quantified with Kodak 1D Image Analysis software.

ELISA

Whole cell extracts were prepared in lysis buffer containing 137 mM NaCl, 20 mM Tris pH 8.0, 1% NP-40, 10% glycerol, 1% protease inhibitor cocktail and 1 mM phenylmethylsulphonyl fluoride. Samples were acidified to pH 2.6 for 15 minutes at room temperature, then neutralized to pH 7.6. The medium from each culture dish was concentrated 10-fold prior to ELISA using Amicon Ultra centrifugal filter devices (5000 MWCO, Millipore). IGF-1 was assayed using the Quantikine® sandwich ELISA kit (R&D Systems), and NGF and NT-3 were assayed using the Emax® immunoassay system (Promega), according to manufacturer's instructions. As the immunogen for the anti-NGF detection antibody is the 2.5S mNGF, this ELISA may also detect proNGF. The trophic factor levels in the media are expressed as the original concentrations in culture.

Acetylcholine assay

Cellular acetylcholine levels were determined by HPLC as previously detailed(Lopez-Coviella et al., 2000). Briefly, cells were incubated in physiological salt solution containing 15 μM choline and 15 μM neostigmine for 1 hour at at 37°C. Cells were washed and collected into 100% MeOH. Precipitated proteins were removed by centrifugation and the supernanant was chloroform extracted. The aqueous layer was lyophilized, then resuspended in diH2O and subject to analysis by HPLC.

Statistics

The statistical significance of changes in protein levels, mRNA expression and ACh content was determined by one-way or two-way ANOVA, as appropriate. All post-hoc analysis were done using Fisher's least-significant-difference test, with p ≤ 0.05 deemed as significant. Specific p values are noted in the figure legends. All error bars indicate the standard error of the mean.

Results

BMP9 modulates the trophic factor profile of basal forebrain cultures

Trophic factors known to play various roles in the development and support of BFCN were examined in murine septal cell cultures in response to BMP9. Cultures were established from cells isolated at embryonic day (E)14 (when Chat expression is very low in vivo), E16 and E18 (after many cholinergic neurons have developed in the septum). After 4 days in vitro, cell lysates and culture media were examined by ELISA for levels of NGF, NT-3 and IGF-1 protein. The addition of BMP9 to the culture media significantly increased the amount of NGF protein both within cells and released into the culture medium at all developmental stages examined (Fig. 1A, B). Intracellular NT-3 levels were significantly decreased by BMP9 treatment at later embryonic stages, while IGF-1 was unaffected. The ELISA results were in agreement with the modulation of Ngf and Ntf3 (encoding NT-3) gene expression by BMP9 (Fig. 1C). As mRNA and protein levels were examined at the same time point, the modest increase in Igf1 gene expression may not have been translated into detectable increases in protein.

Figure 1
BMP9 stimulates NGF production by embryonic septal cells

In order to ensure that the expression of Ngf in septal cells shown here is not a culture-specific phenomenon its expression was also evaluated in uncultured septal tissue over a range of developmental stages, and was found to peak at or around P8 (Fig. S2A). Various early postnatal brain regions were also examined. Though Ngf expression was markedly lower in the septum than in the hippocampus, it was comparable to that measured in the frontal cortex and cerebellum (Fig. S2B).

BMP9-induced Ngf expression in post-mitotic cells, requires new protein synthesis and is mediated by the canonical BMP signaling pathway

A delay in the increased production of NGF protein following BMP9 treatment was observed when shorter duration cultures were examined (Fig. 1D), which correlated with a delay in increased Ngf mRNA levels (Fig. 2A, Control). We hypothesized that this delay was due to either the production of BMP9-induced NGF by dividing cells that can accumulate in septal cultures over time, or an intermediate factor that must accumulate in order to mediate the effects of BMP9. Blocking the expansion of dividing cells with the cytostatic agent cytosine arabinoside (AraC) neither prevented the delay in BMP9-induced Ngf expression nor affected the degree of its induction ultimately achieved (Fig. 2A, 2.2 fold at 96 hours). As expected, the inclusion of AraC in the culture medium yielded a more neuronal cell population as indicated by an approximately 2.5-fold higher Tubb3 (β-3-tubulin) expression as compared to control cultures (Fig. 2B). Likewise, the relative levels of Ngf were approximately 2.5-fold higher in the presence of AraC as compared to the control cultures, independent of BMP9 treatment (Fig. 2B). This suggests that post-mitotic cells are primarily responsible for the production of NGF in septal cultures. Moreover, the expression of a glial cell marker, glial fibrillary acidic protein (Gfap) was abolished by the addition of AraC (Fig. S3), indicating that glial cells are not responsible for the expression of Ngf in the cultures. Conversely, the addition of the protein synthesis inhibitor cycloheximide completely abolished the effect of BMP9 on the expression of Ngf mRNA (Fig. 2A, B), demonstrating that the synthesis of an intermediate factor is necessary for BMP9-induced Ngf gene expression. Although basal expression of Id3 – an immediate downstream target of the Smad signaling pathway activated by BMP9 – was reduced in cultures containing AraC and cycloheximide, it was still greatly increased by BMP9 (Fig. 2B), indicating that BMP signaling remains intact under both conditions.

Figure 2
BMP9-induced Ngf is detected in post-mitotic cells and is dependent on new protein synthesis

The expression of Id genes is robustly induced by BMPs via Smad1/5/8 phosphorylation (Hollnagel et al., 1999; Yu et al., 2008). To assess whether BMP9 is utilizing this canonical pathway of BMP signaling to increase Ngf gene expression, the BMP type I receptor inhibitor, compound C (aka. dorsomorphin (Yu et al., 2008)) was employed. Pre-treatment of septal cultures with 10 μM compound C blocked Smad1/5/8 phosphorylation in short-term septal cultures treated with BMP9 (Fig. 3A). Because this concentration of compound C was toxic in long-term cultures, lower concentrations were used to assess its effect on BMP9-induced Ngf mRNA levels. BMP9-induced expression of both Id3 and Ngf genes was inhibited in a concentration-dependent manner. BMP9-induced Ngf expression was significantly less in samples containing 1.0 and 2.5 μM of compound C than in samples containing no inhibitor. In addition, compound C at 0.1, 1.0 and 2.5 μM significantly inhibited BMP9-induced Id3 expression (Fig. 3B). These data indicate that BMP9 signaling through the BMP type I receptor pathway is required for the induction of Ngf expression.

Figure 3
BMP type 1 receptor signaling is required for BMP9-induced Ngf expression

NGF contributes to BMP9-stimulated ACh production

The modulation of cholinergic properties of septal neurons by BMP9 bears similarity to the actions of NGF in a variety of ways including increased ACh production and Chat expression. We therefore evaluated whether BMP9-induced NGF contributes to the phenotypic effects of BMP9 by blocking NGF function in BMP9-treated cultures. BMP9-induced ACh production was reduced by a TrkA kinase inhibitor (Calbiochem #648450) in a concentration-dependent fashion by as much as 46% (Fig. 4A, ** p=0.0001). The TrkA inhibitor also slightly decreased basal levels of ACh in the absence of BMP9, though this reduction did not achieve significance († p=0.15). To determine whether NGF also contributes to BMP9-modulated gene expression, a highly specific NGF neutralizing antibody (anti-NGF) was added to septal cultures prior to and during BMP9 treatment. This antibody completely blocks NGF-induced TrkA phosphorylation in septal cultures (data not shown). In the presence of anti-NGF the BMP9-induced Chat expression was reduced by 45% (Fig. 4B, **p=0.006), similar to the magnitude of the decrease in ACh content observed with the TrkA inhibitor. In contrast, anti-NGF did not alter BMP9-induced changes in Ngfr (the gene encoding p75), Id3 or Ntrk1 mRNA expression.

Figure 4
BMP9-induced NGF is an autocrine/paracrine factor that stimulates ACh production and Chat expression

BMP9-induced Ngf is restricted to cholinergic neurons

Studies performed in adult rats show that Ngf mRNA is expressed at low levels in the basal forebrain (Large et al., 1986; Shelton and Reichardt, 1986; Lauterborn et al., 1991; Saporito et al., 1994; Saporito and Carswell, 1995), and detected primarily in GABAergic neurons (Lauterborn et al., 1995). The expression of Ngf is not well characterized during development, but it has been detected in the basal forebrain during both embryonic and postnatal periods (Large et al., 1986; Luesse et al., 1998; Formaggio et al., 2010). We hypothesized that embryonic septal cells induced to express Ngf by BMP9 in vitro would be restricted to either a cholinergic or non-cholinergic phenotype. To test this, E14 septal cells from transgenic mice that express enhanced green fluorescent protein (eGFP) under the control of the Chat promoter (Chat-eGFP) (Tallini et al., 2006) were cultured with or without BMP9 in the presence of AraC for 4 days. Fluorescent and phase contrast photomicrographs of the BMP9-treated culture revealed a highly neuronal population of both cholinergic and non-cholinergic neurons that have elongated processes (Fig. 5A). Cultures were further analyzed by flow cytometry. Although Chat expression is minimal in septal neurons at E14, after 4 days in vitro we detected fluorescence in 5.7% of the cultured cells (Fig. 5B, top panel). This likely represents cells already set on a cholinergic differentiation pathway at the time of isolation, or the differentiating influence of endogenous factors or factors present in the basal culture medium. Septal cells treated with BMP9 had almost twice as many eGFP+ cholinergic neurons (9.2%; Fig. 5B, lower panel). Interestingly, the mean fluorescent intensity (MFI) of the cholinergic neurons was similar in both samples (untreated: 143, BMP9: 156) indicating that BMP9 is primarily inducing new cells to express Chat rather than increasing its level of expression in already cholinergic neurons. These eGFP- and eGFP+ cell populations obtained by FACS following a 4-day culture period in the presence and absence of BMP9 were then examined by RT-PCR to measure gene expression levels. As expected, the cholinergic neurons were greatly enriched in Chat and Ngfr mRNA expression in comparison to non-cholinergic cells (Fig. 5B). Ngf expression was detected at low levels in both the cholinergic and non-cholinergic populations collected from the untreated culture. Surprisingly, increased Ngf expression in the BMP9-treated culture was restricted to cholinergic neurons (fold changes in duplicate experiments: eGFP- = 1.0 ±0.1, eGFP+ = 9.5 ±1.2), suggesting that these cells are the source of the functional NGF measured above. Consistent with the similar MFIs of cholinergic neurons isolated from untreated and BMP9-treated cultures, these two populations of cholinergic neurons expressed similar levels of Chat mRNA (Fig. 5B). Gfap expression was not detectable in any sample (data not shown).

Figure 5
BMP9-induced Ngf is expressed in cholinergic neurons

The expression of Ngf mRNA in cholinergic neurons from the developing forebrain was confirmed in freshly isolated cells from ChAT-eGFP mice. A distinct set of eGFP+ cells is present in the septal cell population of Chat-eGFP mice (Fig. 5C), whereas fluorescence is not detectable in cells from this region of wildtype mice. As expected, freshly isolated FACS-sorted eGFP+ cells from E18 Chat-eGFP mice are highly enriched in expression of the cholinergic markers Chat, Ngfr and Slc5a7 (the high-affinity choline transporter, Fig. 5D). Ngf was equally expressed in the cholinergic and non-cholinergic populations.

BMP9-induced Ngf expression becomes restricted to late embryonic p75+ basal forebrain neurons in correlation with their expression of Alk1

Maturing BFCN were purified at E18 using FACS based on cell surface levels of p75, a well-established marker for BFCN in the septum (Dawbarn et al., 1988; Hartikka and Hefti, 1988b; Heckers et al., 1994; Lin et al., 2007). Approximately 7.5% of the E18 septal cell population had detectable p75 protein labeling (Fig. 6A). The p75- and p75+ populations were collected and cultured under conditions previously shown to maintain a highly neuronal cell population (Schnitzler et al., 2008b, a). The cultured p75+ and p75- neurons maintained similar levels of Ngf mRNA (Figure 6B), yet BMP9 treatment only increased Ngf levels in p75+ cells. This result suggests that even though Ngf is expressed in, at least some, cholinergic and non-cholinergic septal cells, the further augmentation of Ngf expression by BMP9 is also restricted to BFCN during late embryogenesis. Importantly, the highly enriched expression of Ntrk1 in p75+ septal neurons was maintained with BMP9 treatment (Fig. 6C).

Figure 6
Augmentation of Ngf expression by BMP9 in mature, p75-expressing BFCN

Because the pattern of TGFβ receptor expression fine-tunes responses to BMPs, we compared the levels of select receptors in p75- and p75+ septal cells (Fig. 6D). Interestingly only p75+ cells expressed the mRNA for the type I BMP9 receptor, Alk1/Acvrl1 (Brown et al., 2005), while p75- cell were devoid of this message. The expression of the other type I BMP receptors (Alk2/Acvr1, Alk3/Bmpr1a, Alk4/Acvr1b and Alk6/Bmpr1b) and of the type II receptors (Bmpr2, Acvr2a/ActrII and Acvr2b/ActrIIb) was similar in p75+ and p75- cells. These data point to ALK1 as a novel marker for BFCN and suggest that ALK1 might mediate the upregulation of NGF production in response to BMP9 specifically in the p75+ neurons.

Discussion

The central findings of this study are that Ngf mRNA is expressed in cholinergic (Chat- or p75-expressing) and non-cholinergic cells of the developing basal forebrain, and that in vitro BMP9 stimulates the expression and release of NGF that contributes to the BMP9-induced upregulation of the cholinergic phenotype of BFCN. The restriction of BMP9-induced Ngf expression to cholinergic neurons suggests and autocrine/paracrine function of NGF in this system. In addition, these data together with our observation that BMP9 dramatically reduces the production of NT3 and increases Igf1 mRNA levels in septal cultures point to a novel mode of BMP9 action, i.e. modulation of the trophic environment of developing basal forebrain neurons. Consistent with previous results (Lopez-Coviella et al., 2005; Schnitzler et al., 2008a), the Ngfr mRNA and cell surface protein levels rose several-fold in cells treated with BMP9. The increased expression of Ngfr would be expected to potentiate NGF signaling via TrkA (Canossa et al., 1996). Conversely, p75 can act as mediator of apoptosis (Dechant and Barde, 2002; Chao, 2003) and, when secreted by cells, as a possible soluble inhibitor of NGF (Weskamp et al., 2004). BMP9 also induces the expression of noggin (Lopez-Coviella et al., 2005), a soluble antagonist of BMP action. These observations demonstrate that BMP9 also regulates the expression of molecules that govern BFCN responses to NGF and BMPs.

NGF-evoked induction of Chat and upregulation of ACh production requires Ntrk1 expression and activity (Berse et al., 1999), and indeed the increase of cellular ACh levels evoked by the BMP9-induced NGF synthesis was sensitive to TrkA inhibition. TrkA is a marker of the cholinergic cell bodies in the septum and NGF infusion in vivo elicits TrkA phosphorylation, increases the size of cholinergic neurons and stimulates Chat expression (Li et al., 1995). BMP9 appears to target the already differentiated cholinergic neurons at later embryonic stages to increase NGF expression. As these neurons are highly enriched in Ntrk1 expression, an autocrine system that can be modulated by BMPs is implicated. Moreover, BMP9 increases Chat mRNA expression in SN56T17 cells (Lopez-Coviella et al., 2000) and in purified p75-expressing BFCN (Schnitzler et al., 2008a), suggesting that its action does not require the presence of auxiliary cells.

The possibility of a NGF/TrkA mediated autocrine system was previously suggested by studies on the cell bodies of layer V pyramidal neurons of the adult rat cortex where dual fluorescent in situ hybrization and immunolabeling of histological sections revealed co-expression of Ngf mRNA and phospho-TrkA protein (Bruns and Miller, 2007). During adulthood, NGF supplied to the basal forebrain via retrograde transport from the target regions is a major source of the growth factor (Sofroniew et al., 2001). However, during development efferents from the septum to the hippocampus are first detected in late embryonic stages, and the adult pattern of innervation is not established until after P10 (Linke and Frotscher, 1993). Though the administration of exogenous NGF to adult mice with a single disrupted Ngf allele can ameliorate select behavioral and morphological deficits associated with NGF haploinsufficiency, it does not rescue the reduced cholinergic cell number in the septum (Chen et al., 1997). Together, these data suggest that NGF deficiency during development can permanently alter neural architecture in the mature animal, and that the locally derived NGF reported here may be particularly important during developmental stages prior to complete target innervation.

At least one cell type that produces neurotrophins in the developing forebrain has been identified. Astrocytes isolated from the P1 rodent forebrain express NGF, BDNF and NT-3, and can modulate their expression in response to a variety of neuronal signals (Wu et al., 2004). Astrocytes in other brain regions have been shown to express p75, raising the questions whether the increased NGF expression that we detect in p75+ cells from the septum is due to an early astrocytic cell population. Even though there is no published evidence that embryonic astrocytes in the septum express p75, our data do not eliminate this possibility. However, the continued strong expression of Ntrk1 in the purified p75+ cells in culture, the expression of Ngf in freshly purified Chat-eGFP+ BFCN, its induction by BMP9 in Chat-eGFP+ BFCN isolated from E14 cultures, concomitant with the apparent absence of glial cells in the cultures (as determined by undetectable levels of Gfap mRNA) support an autocrine paradigm.

We found several type I and type II BMP receptors expressed in both p75- and p75+ cells from the prenatal mouse septum, some of which are reportedly responsive to BMP9 (Massague, 2008). These receptors are likely responsible for the robust induction of cholinergic genes in p75- septal cells by BMP9 (Schnitzler et al., 2008a). The current results also show that p75+ cells express Alk1 while p75- do not and thus point to the possibility that ALK1 is responsible for the specific induction of NGF by BMP9 in maturing BFCN (p75+ cells). The restricted expression of Alk1 to p75+ cells may also make it a useful marker for at least a subset, if not all, cholinergic neurons in the developing septum. Importantly, ALK1 has been shown to interact directly with BMP9 (Brown et al., 2005), and is sensitive to compound C (Upton et al., 2009) – a type I receptor inhibitor that abolished BMP9-activated SMAD1/5/8 phosphorylation as well as Id3 and Ngf induction. Moreover, our previous studies showed that SMAD1 and SMAD5 are robustly expressed in the fetal septum, and both become highly phosphorylated, form a complex with SMAD4 and translocate to the nucleus in E14 septal cells treated with BMP9 (Lopez-Coviella et al., 2006). Thus, the broadly-defined canonical BMP signaling pathway is activated by BMP9 in septal cells and is likely required for BMP9-induced Ngf expression.

The induction of Ngf mRNA in septal cultures by BMP9 was abolished by treatment with cycloheximide, indicating that it required the synthesis of a protein mediator – possibly a transcription factor. BMP9 rapidly stimulates the expression of multiple transcriptional regulators and several of these molecules are critical for normal neuronal development, including Gata2, Msx1, Msx2, Zfp423 (Roaz), Id1 and Id3 (Lopez-Coviella et al., 2005). In the current study we used the expression of the latter as an example of a direct target gene (i.e. insensitive to cycloheximide) of BMP action. There are no data on the regulation of Ngf expression by these proteins, however they constitute a set of targets for further studies. Another potential candidate may be p75 which is upregulated by BMP9, and has been shown to affect transcriptional signaling pathways after proteolytic release of its intracellular domain (Kanning et al., 2003), though there is currently no evidence that this mechanism regulates Ngf expression. In addition to transcription factors, BMP9 may modulate the expression of diffusible molecules that affect NGF production. For example, we reported that BMP9 upregulates the expression of ciliary neurotrophic factor (Cntf) in septal cultures (Lopez-Coviella et al., 2005), a protein that increases Ngf expression in astrocytes (Semkova and Krieglstein, 1999), Ngfr expression in septal cultures (Magal et al., 1991) and Chat expression in sympathetic neurons (Saadat et al., 1989). Moreover, BMPs have been shown in a number of nervous system regions and experimental models to interact functionally with neurotrophins to promote neuronal survival and function. For example, BMPs synergize with neurotrophins to preserve ChAT activity in cultured embryonic septal neurons under hypoglycemic stress (Nonner et al., 2001). It is possible that BMP9 not only increases the production of NGF, but also enhances its efficacy. The current results that BMP9 specifically targets BFCN to express Ngf together with data showing BMP9 can increase ChAT activity, ACh production and Ngfr expression suggest a multifactorial role for BMP9 in supporting the cholinergic phenotype.

Supplementary Material

Supp1

Acknowledgments

We thank Yanhui Deng and the Boston University Medical Center Flow Cytometry Core Facility for providing expertise in fluorescence activated cell sorting. This work was supported by NIH grants AG009525, AG032709, and DK065992.

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