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Fatty acids are central to brain metabolism and signaling, but their distributions within complex brain circuits have been difficult to study. Here we applied an emerging technique, time-of-flight secondary ion mass spectrometry (ToF-SIMS), to image specific fatty acids in a favorable model system for chemical analyses of brain circuits, the zebra finch (Taeniopygia guttata). The zebra finch, a songbird, produces complex learned vocalizations under the control of an interconnected set of discrete, dedicated brain nuclei “song nuclei”. Using ToF-SIMS, the major song nuclei were visualized by virtue of differences in their content of essential and non-essential fatty acids. Essential fatty acids (arachidonic acid and docosahexaenoic acid) showed distinctive distributions across the song nuclei, and the 18-carbon fatty acids stearate and oleate discriminated the different core and shell subregions of song nucleus LMAN. Principle component analysis of the spectral data set provided further evidence of chemical distinctions between the song nuclei. By analyzing song nucleus RA at three different ages during juvenile song learning, we obtain the first direct evidence of changes in lipid content that correlate with progression of song learning. The results demonstrate the value of ToF-SIMS to study lipids in a favorable model system for probing the function of lipids in brain organization, development and function.
Fatty acids comprise a diverse group of unbranched carboxylic acids, with variable numbers of carbon chains and degrees of saturation. They are central in cell metabolism and also form a primary structural component of all cell membranes (as phospholipids). They also have major roles in cell signaling – and nowhere more so than in the brain. Membrane phospholipids are precursors for the generation of numerous messenger compounds active in the brain including prostaglandins and platelet-activating factor (Bazan, 2005), endocannabinoids (Piomelli, 2005), and diacylglycerol (Kim et al., 2010). Local variations in specific lipid content contribute to the structure of synaptic junctions (Suzuki, 2002), and growing evidence suggests that specific synaptic lipids regulate vesicle exocytosis and membrane recycling (Davletov & Montecucco, 2010). Of particular interest are the essential fatty acids (EFAs) – polyunsaturated fatty acids that are derived from the diet and important in in cognitive function (Moriguchi et al. 2000), inflammatory and immunological responses (Simopoulos, 2002; Bazan, 2005), and brain development (Innis, 2008). Polyunsaturated fatty acids (PUFAs) are notably vulnerable to oxidative damage (and conversely, may also participate in protection against oxidative damage) and have been implicated as promoting or protective factors in a range of neurological diseases, including Alzheimer's (Hartmann et al. 2007), Parkinson's (Israeli & Sharon 2009) schizophrenia (Fenton et al. 2000) and epilepsy (Cole-Edwards & Bazan 2005).
A better understanding of the diversity of fatty acids and their specific local distributions and functions will therefore be critical for a broad range of issues in neurobiology. However, the tools for studying fatty acid distributions in brain have been limited compared to the tools available for analysis of proteins and nucleic acids. Studies have typically relied on dissection, homogenization, and detection – methods that do not provide information about cellular or subcellular distributions. Specific lipids can be visualized with fluorophore labels but this is limited to cases where labeled lipids can be applied exogenously, and these labels can adversely affect lipid-lipid and lipid-protein interactions (Maier et al. 2002).
Time-of-flight secondary ion mass spectrometry (ToF-SIMS) is an alternative approach that allows direct surface visualization of intrinsic, unlabeled small molecules (<1,000 m/z) in tissue sections at a lateral resolution of ~1 μm (Ewing 2006, Johansson 2006, Mas et al. 2008). The technology has been shown to be a robust tool for the detection and imaging of lipids in a diverse array of tissues such as muscle (Tahallah et al. 2008), nervous system (Pernber et al. 2007), and kidney (Nygren et al. 2004). Subcellular imaging with ToF-SIMS has also revealed significant localization of other lipophilic molecules such as vitamin E in isolated neurons from Aplysia californica (Monroe et al. 2005) and has been used in several studies on the mammalian spine (Monroe, et al. 2005, Monroe et al. 2008).
In this report, we describe the application of ToF-SIMS to develop a primary analysis of the distribution of fatty acids within the brain of both adult and developing zebra finches. The zebra finch (Taeniopygia guttata), a songbird, is an important model for neuronal circuitry development, neurogenesis, learning and memory, and its genome was recently sequenced (Warren et al. 2010). A distinctive feature of the songbird brain, which makes it especially conducive to focal molecular analysis, is the presence of several large anatomical nuclei in the forebrain that are interconnected in a circuit (Fig. 1) that controls the learning and production of birdsong (reviewed in (Brenowitz et al. 1997, Clayton et al. 2009, Zeigler & Marler 2004). These nuclei have been studied intensively for their physiological and developmental properties (Clayton 1997) and they form a valuable reference set for studies of molecular composition in the brain (Lovell et al. 2008). In the zebra finch, this “song control circuit” is completed during a critical period in juvenile development (between about 20 and 40 days post-hatch), and only in males (females do not produce learned vocalizations). It is during this critical period that a young male zebra finch learns to sing by copying the song of an adult tutor. With sexual maturity, the ability to further modify the song or learn a new one is essentially lost.
Several observations suggest important roles for lipids and fatty acids in song system development and function. One of the first genes shown to be developmentally regulated within the song control circuit encodes the ortholog of alpha-synuclein (originally referred to as synelfin, (George et al. 1995)), a lipid-binding protein subsequently implicated in Parkinson's and other neurodegenerative diseases (Clayton & George 1999). Lipophilic molecules, including retinoic acid (Jeong et al. 2005, Denisenko-Nehrbass et al. 2000), cannabinoids (Soderstrom et al., 2004) and sex steroids (London et al. 2006), are synthesized in or near several of the song control nuclei and are necessary for song learning and song circuit development. Yet the lipid and fatty acid composition of the zebra finch brain has remained largely unexplored. Indeed, information about brain lipids is sparse for all birds in comparison to mammals, and mostly limited to issues related to embryogenesis, metabolic rate and egg production (e.g., (Maldjian et al., 1996; Speake & Wood, 2005; Turner, 2005).
We previously used ToF-SIMS to image the distributions of several inorganic ions and lipids in the songbird brain (Amaya et al. 2007). Here we analyze the distribution of fatty acids and other lipids across the major forebrain components of the song system, both in adults and during the critical period for song learning and circuit development. In order to facilitate analysis of the complex datasets, we incorporate principle component analysis (PCA) into our measurements to determine regional and age-related differences in content. Our results reveal a complex distribution of fatty acids across different song nuclei, and set the foundation for future targeted studies to address the potential functional importance of these fatty acids in this important model of neural circuit development and function.
All animal procedures were conducted according to protocols approved by the University of Illinois Institutional Animal Care and Use Committee. Male zebra finches were sacrificed by rapid decapitation, the brain removed, and rapidly frozen on dry ice. Post-hatch day 20 birds were sexed postmortem by gonadal identification. Parasagittal sections, 16 μm in thickness, were collected beginning at 2.5 mm to the midline (~5.6 mm) and alternatively placed on either a glass slide for histological staining, or a glass cover slip for ToF-SIMS and immunohistochemical analyses. Sections were stored at –80 °C for no more than 3 wks. Histological staining by cresyl violet was carried out as previously described (Amaya et al. 2007). Sections were identified that contained the major components of the forebrain song system: nucleus RA, nucleus HVC (used as a proper name), lateral magnocellular nucleus of the nidopallium (LMAN), dorsolateral thalamic nucleus (DLM), AreaX, and the NCM/CMM complex comprising the AL (Fig. 1). The adjacent sections then used for ToF-SIMS or immunohistochemical analysis.
Sections from adult males (n=3) were removed from –80 °C storage and immediately vacuum dried (~15 min) at room temperature. Dried sections were placed in a Desk II TFC sputter coater (Denton Vacuum, Moorestown, NJ) equipped with a gold target and ~10 Å was deposited on sample surface to improve the ionization of surface molecules (Altelaar et al. 2006). ToF-SIMS analyses were conducted in the Materials Research Laboratory facilities at the University of Illinois at Urbana-Champaign (UIUC); specifically, the instrument used was a TRIFT ToF-SIMS mass spectrometer (Physical Electronics, Chanhassen, MN) equipped with a gold liquid metal ion source. The primary ion beam used Au1 running at 22 keV, 2 nAmp, and the primary ion dose was kept below the static limit of 1 × 1013 primary ions cm-2 and negative secondary ions collected. Mass spectrometric images were collected using WinCadence software (Physical Electronics, Chanhassen, MN) with its built-in mosaic function, except HVC which was collected as two 600 × 600 μm images. Images measuring 1 × 1 mm were composed of 16 steps, each interrogating 250 × 250 μm; the areas of 1.5 × 1.5 mm also were composed of 16 steps, now measuring 375 × 375 μm each. Images containing HVC and AL were stitched as previously described (Amaya et al. 2007). Individual images are composed of 256 × 256 pixels with each pixel representing a unique mass spectrum of the sample surface. All images were convolved once using the default settings in WinCadence and individually scaled to a relative intensity scale of 0 - 100%. Where multiple ToF-SIMS images are shown to compare distributions of different molecules within a single song nucleus, all images are from the same individual tissue section. Qualitative descriptions of histological patterns described in Results are based on observations made in all three adult males, though only a single representative section is shown in each figure. Where additional procedures were performed (i.e., cresyl violet, IHC) these were performed on sections serially adjacent to the section used for ToF-SIMS.
After determining the likely fatty acids based on mass matching, our putative identifications relied on comparing the spectra from the brain tissue with spectra from standards purchased either from Sigma-Aldrich or Cayman Chemical (> 95% purity). Standards were either adhered to or deposited on carbon tape and subjected to ToF-SIMS analysis and their mass to charge ratio recorded (Table 1). We confirmed our assignments of these fatty acids in the brain using an alternative approach; more specifically, the region of interest was removed, lipids extracted, and fatty acids analyzed by GC-MS (Supplemental S1 and S2). To determine if esterified lipids undergo chemical fragmentation, a standard of phosphatidylethanolamine (PE) purity of ~ 98% (Sigma-Aldrich) was adhered to carbon tape and subjected to ToF-SIMS analysis (Supplemental S3).
For multivariate statistical analysis, mass spectra from the song nuclei from three different males were collected by using the region of interest function (ROI) in WinCadence. The developmental comparison consisted of three different males, for each age group, with ToF-SIMS collected from five different 200 × 200 μm areas within RA. Spectra were box binned and normalized to carbon (m/z 12), a ubiquitous and biologically significant ion. Contaminating peaks and peaks <m/z 50 were excluded from data analysis. PCA was carried out using PLS_Tool box (Eigenvector Research, Inc. Wenatchee, WA), and data were preprocessed by autoscaling and transformed to a logarithmic scale (log10) to ensure high-intensity peaks were not overrepresented (Wagner et al. 2004).
Sections were removed from –80 °C storage and fixed with 4% paraformaldehyde (pH 7.3) for 5 min and washed three times with 0.025 M PBS (pH 7.0) for 5 min each time. Tissue was blocked for 1 h at room temperature in a humidity chamber with Image-iT FX signal enhancer (I36933, Invitrogen, Carlsbad, CA), followed by a TBS-TX (50 mM Tris HCl, pH 7.4, 150 mM NaCl, and 0.1% Triton-X-100) wash (5 min, × 3). A second blocking step with TBS-TX plus 10% normal donkey serum was done, followed by a TBS-TX wash step.
Sections were then incubated with primary antibodies against the neuronal marker, NeuN 1:500, (MAB377, Millipore, Billerica, MA) and myelin basic protein, MBP 1:75, (AB9348, Millipore) at room temperature in a humidity chamber. After 1 hr tissues were washed with TBS-TX and incubated 1 hr with the secondary antibodies Alexa 488 (A-21202, Invitrogen) and Alexa 546 (A11040, Invitrogen) diluted 1:500, followed by a TBS-TX wash. Cell nuclei were stained with DAPI (12 μg/mL) for 5 min, washed with TBS-TX, and cover slip mounted with ProLong Gold (P36934, Invitrogen). Slides were then analyzed under a Zeiss Axiovert 200M (Carl Zeiss Microimaging, Inc., Thornwood, NY) fluorescence microscope on site at the Institute for Genomic Biology core facilities, UIUC.
From ToF-SIMS data for each brain section examined (n=3 birds), images were constructed for 13 fatty acids and cholesterol. Using the ROI function, relative concentrations were assessed within the five major song nuclei and the two major subdivisions of the AL (Table 2). By ANOVA, there were significant differences among these brain regions for nine of these lipids, with the largest effect (nearly four-fold) observed for the long polyunsaturated EFA, arachidonic acid (ARA, 20:4 n-6).
Individual song nuclei were readily distinguishable from the surrounding brain tissue by their content of these lipids. Figure 2 presents an overview of the relative content of these lipids in nucleus RA compared to the surrounding arcopallium and nidopallium, in a single tissue section (images of additional song nuclei and at larger magnification are presented in Supplemental S4-S6). As reference and for comparison to conventional histological methods, adjacent sections were stained using cresyl violet and immunohistochemistry. Cresyl violet staining (Fig. 2B) shows this well-defined song nucleus sitting within the arcopallium and just below (ventral to) the nidopallium. Immunohistochemical labeling with the neuronal marker NeuN (Fig. 2C, green) shows robust labeling of the RA and significant labeling in the nidopallium, but little to no staining in the surrounding arcopallium. Myelin labeling (Fig. 2C, red) shows a clear demarcation and a more intense overall labeling of the RA compared to the arcopallium or nidopallium. Punctate areas of intense labeling in the anterior part of the arcopallium likely correspond to fiber tracks connecting RA to fasciculus prosencephali lateralis, and striations in the nidopallium are neuronal projections that connect the HVC and RA. The labeling of cell nuclei with DAPI (blue) shows no discernable difference in cell density across the image. ToF-SIMS analysis of palmitic acid (16:0) produces a striking image as this lipid is sharply enriched within the boundaries of nucleus RA, with intermediate labeling in the surrounding arcopallium and lower labeling in the overlying nidopallium (Fig. 2D). Fig. 2E summarizes the relative signal intensities for all 13 fatty acids and cholesterol in RA compared to surrounding tissue in this same brain section.
The omega-3 and omega-6 unsaturated EFAs are of particular interest given their importance in cell signaling, brain function, and therapeutics. A survey of the local distributions of these in and around the six song system regions is presented in Figure 3. (Selected images are also shown aligned with reference sections in Supplemental S4. A similar series is shown for non-essential fatty acids in Supplemental S6). Eicosapentaenoic acid (EPA, 20:5 n-3) and arachidonic acid (ARA, 20:4 n-6) are notably reduced in the RA, especially in comparison to the nidopallium (Fig. 3C, D). In contrast, docosahexaenoic acid (DHA, 22:6 n-3) shows increased relative levels in the RA compared to surrounding tissue, as do the EFAs linoleic acid (18:2 n-6) and 11,14-eicosadienoic acid (20:2 n-6). The EFAs 8,11,14, eicosatrienoic acid (20:3 n-6) and adrenic acid (22:4 n-6) are not included in the figure as they show no difference in spatial distributions within these nuclei compared to the surrounding tissue, even though they do show differences in levels within different song nuclei (Table 2). Nucleus LMAN, which projects to RA, and its thalamic afferent (DLM) are generally similar to RA for all these EFAs. HVC also projects to RA, but HVC generally shows less differential content of the EFAs compared to surrounding tissue, with little or no enrichment for linoleic acid nor a reduction in ARA. Area X shows little differential content except for a reduction in ARA. The AL shows evidence of internal subdivisions according to the different distributions of EPA, DHA and ARA.
The song control nucleus LMAN is essential for song learning, and has been described as having a central core of magnocellular neurons surrounded by a shell of parvicellular neurons, with discrete functions proposed for these two subregions (Johnson et al. 1995, Bottjer & Altenau 2010). We noted variation in the anatomical pattern of several lipids across this nucleus and analyzed this in further detail by line scan. ToF-SIMS imaging of the LMAN indicates reciprocal internal distributions of the monounsaturated 18-carbon fatty acid, oleic acid, and the fully saturated form, stearic acid (Fig. 4A, B). Linescan analysis, moving across the images from the upper left to the lower right, quantifies these distributions at each pixel (Fig. 6C). Oleic acid (red line) shows a significant increase in relative signal intensity in the area corresponding to the core of the nucleus. Stearic acid (blue line) shows two spots of maximum signal intensity extending over an area of ~150 μm (Fig. 6C). Both areas of increased stearic acid signal are immediately adjacent to the increased oleic acid signal. Comparing the two images it appears the increased stearic acid signal encircles the increased oleic acid signal (Fig. 6A, B). This is consistent with the prior descriptions of core/shell regions (Johnson et al. 1995, Bottjer & Altenau 2010). Direct overlap of IHC and ToF-SIMS images from adjacent sections (not shown) indicates the lipids are concentrated mostly outside of neuronal nuclei but we cannot discriminate whether they are present in glia or neuropil.
The observations above reveal that known chemicals individually show clear differences in distribution across the major song nuclei. We used PCA to analyze at once the entire set of SIMS spectra from each of the three birds, considering all five song nuclei plus NCM and CMM in the AL (Fig. 5). Principle component 1 (PC1, x-axis) captures 55% of the variation in the data. Much of the variation is between the chemical profiles of the NCM/CMM and RA, along with one spectrum from the LMAN (Fig. 5A). Analysis of the corresponding loadings plot (Fig. 5B) reveals that the NCM/CMM region has the greatest association (increased relative amount) with m/z 79 (phosphate), m/z 122 (ethanolamine), and three unknown peaks (m/z 81, 153, 124). The same loadings plot shows that the RA and one LMAN spectrum have a relative increase in peaks corresponding to four fatty acids: m/z 255 (palmitic acid), m/z 227 (myristic acid), m/z 309 (11-eicosenoic acid), and m/z 327 (DHA) as compared to the NCM/CMM. Spectra from the other song nuclei show little variation in relation to the NCM/CMM and RA based on their position near the x-axis. Principle component 2 (PC2, y-axis) accounts for 16.44% of the variation and captures major differences between striatal nucleus AreaX and the thalamic song nucleus DLM, along with some spectra from the RA and LMAN (Fig. 5A). Much of the difference is captured by an unknown peak, m/z 124, showing relative abundance in AreaX. Other peaks highly associated with AreaX include m/z 565, m/z 163, m/z 153, m/z 63, m/z 79 (phosphate) and m/z 122 (representing phosphoethanolamine) (Fig. 5B). Along PC2 of the corresponding loadings plot, peaks corresponding to m/z 327 (DHA), m/z 309 (11-eicosenoic acid), m/z 283 (stearic acid), and m/z 281 (oleic acid) show higher relative levels in the DLM and some spectra from the RA and LMAN as compared to AreaX (Fig. 5). Spectra from the NCM, CMM, HVC, and some RA tissue show little variation compared to the DLM and AreaX based on their proximity to the y-axis (Fig. 5A).
We examined male birds at three different ages, corresponding to just before onset of the critical period for song learning and circuit maturation (post-hatch day 20, p20), the peak of the critical period (p40) and adulthood (>p90). PCA comparing RAs from three male birds at each age shows significant separation between adult and p20 RAs (Fig. 6A); in contrast comparing SIMS data collected from 5 unique areas within each RA shows less variation. Most of the age-related separation is along PC2, accounting for 21.26% of the total variation in the spectral data, while PC1 accounts for 66.25% of the variation and appears to capture inherent biological variation (Fig. 6A). Analysis of the corresponding loadings plot for PC2 reveals that m/z 79 (phosphate), m/z 124 (unknown), and m/z 122 (phosphoethanolamine) are the major peaks associated (increased relative abundance) with RAs from p20 birds compared to adults (Fig. 6B). The loadings plot also shows that RAs from adult birds show greatest association (relative abundance) with high molecular peaks m/z >800, along with some fatty acids including: DHA (m/z 327), 11-eicosenoic acid (m/z 309), and stearic acid (m/z 283), in addition to a peak previously identified as vitamin E (m/z 429) (Fig. 6B).
ToF-SIMS is a sensitive surface analysis method relying on the bombardment of a primary ion to analyze the top few layers of a sample surface (Sodhi 2004). In the past, extensive chemical fragmentation has limited its application for imaging larger molecules from biological tissues; however this limitation has been ameliorated by using cluster ion sources (Brunelle et al. 2005) and higher molecular weight primary ions (Fletcher et al. 2006). The results presented here confirm the use of ToF-SIMS as a valuable tool used to uncover chemical heterogeneity and the local distributions of fatty acids within the complex anatomy of brain tissue sections. It may also complement conventional histological and immunocytochemical staining procedures for analysis of brain anatomy, as we have shown here using the zebra finch song control system, finding new neuroanatomical features not evident with these other techniques.
A key feature of ToF-SIMS imaging is both a strength and a weakness: it can image the distribution of any peak detected by mass spectroscopy, without requiring any pre or post hoc knowledge of the chemical responsible for the peak. Assignment of chemical identities to specific masses is challenging as there is no comprehensive molecular ion database for ToF-SIMS; moreover, ionization patterns potentially vary within different subregions of the same tissue section based on variation in the local chemical makeup (Ostrowski et al. 2005). Topographical features can also affect sputtering of secondary ions (McDonnell et al. 2005); however, our use of cryosectioning minimizes these problems. Although our mass assignments must be qualified as putative, many of them were supported by direct ToF-SIMS analysis of known standards (Table 1) and by GC-MS analysis (Supplemental S1 and S2).
We believe the majority of the fatty acids detected in this study are probably derived from esterified lipids that fragmented upon impact of the primary ion. In support of this, we observed that a pure standard of phosphatidylethanolamine (PE) gave rise primarily to free fatty acids upon ToF-SIMS analysis (Supplemental S3). We also considered the possibility that the signals for the unsaturated EFAs ARA and EPA could have been confounded due to fragmentation. However, we believe these signals represent distinct chemical species present in the tissue since both species were detected in forebrain samples by gas chromatography mass spectrometry (Supplemental S2), and standards subjected to ToF-SIMS exhibited minimal and non-identical patterns of fragmentation (data not shown).
We constructed images showing the simultaneous distributions within individual sections of zebra finch brain for each of 13 well-defined lipids and cholesterol. The anatomical patterns of the various fatty acids generally respected boundaries within the tissue evident by cresyl violet staining or specific immunohistochemistry, though in some cases additional details were evident that were not apparent by these other methods (e.g., Fig. 2D). For example, we noted complementary patterns of several fatty acids associated with song nucleus LMAN, consistent with the presence of distinct “core” and “shell” subregions previously defined by their distinct neuroanatomical projections (Johnson et al. 1995) and different effects of lesion (Bottjer & Altenau 2010). In our data, both of these subregions show enrichment for the saturated 18-carbon fatty acid stearic acid, whereas the shell only is markedly enriched in the monounsaturated form, oleic acid.
In general our results show that each song nucleus can be distinguished by its relative complement of fatty acids, with respect both to the surrounding tissue (Figs. 2 and and3)3) and to the other song nuclei (Table 2), an observation that parallels findings using microarrays and in situ hybridization to measure specific mRNA content (Lovell et al. 2008). We replicated our observations in 3 different adult zebra finch brains, and observed a statistically significant main effect of brain region on signal for 8 of the 14 compounds we explicitly quantified (Table 2). We also used PCA on the entire spectral data set, finding that each song nucleus is discriminated fairly effectively in the first two principal components (Fig. 5). PCA is an unsupervised statistical approach used to reduce large complex chemical data sets into a few manageable variables. It can efficiently extract information representing chemical differences and similarities between samples (Lindon et al. 2007) and has been used in SIMS previously (Sjovall et al. 2004, Wu et al. 2007, Kulp et al. 2006). The clustering of our data according to song nucleus is especially interesting given that our zebra finches are not inbred and still retain robust genetic diversity (Forstmeier et al., 2007). PC1 captures 55% of the spectral variation and seems to segregate the brain regions according sensory versus motor function in the song system. The NCM/CMM is a sensory region that shows significant chemical differences when compared with the RA, which is the motor output nucleus of the telencephalic control system. In contrast, the DLM, HVC, LMAN, and AreaX regions are more clearly involved in both sensory and motor function, and cluster between the RA and NCM/CMM areas. The loadings plot shows a decreased association of the RA, compared to the NCM/CMM, with phosphate and ethanolamine, which may suggest a relative increase in sphingomyelin and glycosphingolipids in the RA (Isaac et al. 2006, Sastry 1985). Along PC2, the major effect is the segregation of the striatal nucleus Area X from the other song regions. Interestingly, AreaX also has a rather different profile of gene expression in the combined microarray studies of the SoNG Initiative (Replogle et al. 2008) (and unpublished).
EFAs are of particular interest given their known roles in cellular signaling and plasticity, and the fact that they are not synthesized locally but must be selectively accumulated from circulating stores derived from dietary sources. The EFAs showed especially marked distribution patterns in song nucleus RA. DHA is notably increased in the RA compared to surrounding brain regions. It is believed that the highly unsaturated nature of DHA provides significant membrane fluidity, required for proper brain function (Bourre et al. 1992) and neuronal development (Calderon & Kim 2004), and a protective role against neurodegenerative disease has been suggested (Oster & Pillot 2010). In other systems, DHA has been shown to be enriched in metabolically active brain areas such as the mammalian basal ganglia and gray matter (Diau et al. 2005), in brain regions with increased synaptic vesicles (McGee et al. 1994), and in nerve growth cones (Martin & Bazan 1992). RA itself has a high level of metabolic activity (Adret & Margoliash 2002) with dense synaptic input from two sources (HVC and LMAN) and a mixture of glutamatergic projection neurons and GABAergic interneurons (Pinaud & Mello 2007).
In contrast to DHA, two other EFAs implicated in brain function, EPA and ARA, are decreased in RA. EPA is a precursor to DHA, suggesting the possibility that RA neurons favor synthesis of DHA at the expense of EPA. ARA is a polyunsaturated fatty acid with multiple roles in cell signaling and synaptic potentiation (Williams et al. 1989), but it also exhibits pro-inflammatory effects by acting as a precursor in eicosanoid synthesis (Simopoulos 2002) and may mediate processes leading to neurodegenerative disease (Sanchez-Mejia & Mucke 2010). Intriguingly, the alpha-synuclein protein (SNCA) is also notably decreased in the RA of the adult zebra finch (George et al. 1995, Jin & Clayton 1997), and it interacts closely with ARA (Darios et al. 2010) and has reciprocal effects on the metabolism of ARA versus DHA (Golovko et al. 2007, Golovko et al. 2009). These observations suggest a concerted regulation within RA of particular lipid pathways that mediate cellular integrity and synaptic plasticity.
In the remaining song regions we also measured localized decreases in ARA, with two exceptions, Area X and the AL (NCM/CMM). AreaX is located in the striatum proper of the basal ganglia and contains both striatal and pallidal neurons, which are composed of mostly small γ-aminobutyric acid (GABA)ergic spiny neurons with fewer large GABAergic neurons (Farries & Perkel 2002, Reiner et al. 2004, Grisham & Arnold 1994, Carrillo & Doupe 2004). AL has a complex internal organization and is the central auditory area engaged in song perception; it shows high levels of both ARA and EPA, especially in the caudal part of the NCM subregion (Fig. 3, Supplemental S5). The AL also shows unique distributions for palmitic acid, stearic acid, and oleic acid (Supplemental S5). Molecular studies of the AL have shown retinoic acid receptors with a similar expression pattern as the distribution of ARA, EPA, and stearic acid (Jeong et al. 2005). Retinoic acid production in the song control system is necessary for normal song maturation (Denisenko-Nehrbass et al. 2000), and in mice it has a role in neuronal plasticity and learning and memory (Krezel et al. 1998, Cocco et al. 2002). The differential distribution of fatty acids may reflect distinct cellular populations in the auditory caudomedial telencephalon, with distinct molecular, anatomical, and physiological properties.
A male zebra finch learns to sing during a discrete “critical period” in late juvenile life. Importantly, the entire song learning process occurs after development is otherwise largely complete and the bird has fledged from the nest. A young male first begins to produce immature vocalizations at about P30, the age at which axons abruptly project from nucleus HVC and form synaptic connections onto the major output nucleus of the telencephalic control system (Fig. 1), nucleus RA (Konishi & Akutagawa 1985, Holloway & Clayton 2001). The bird's vocal performance gradually becomes more refined and stereotyped over the next 4-8 weeks, reaching its mature adult form by ~P90, after which no further change in the song will occur for the rest of the bird's life.
We applied ToF-SIMS to ask whether there were significant differences in lipid composition in nucleus RA before (P20), during (P40), and after (adult) the developmental song learning period. Unlike direct analysis of anatomical distributions observed within individual brain sections, comparisons of sections taken from different animals must confront the potential for artifacts arising from subtle variations in sample preparation. To minimize this risk we used a minimal approach to sample preparation, with the sections simply frozen and then vacuum dried prior to sputter coating, and then employed PCA as a way to objectively include all the spectral data in this analysis (Fig. 6).
Just as our PCA analysis showed a major effect of brain region (Fig. 5), here PCA revealed a major effect of developmental age on the spectral patterns obtained from nucleus RA, especially along the axis of the second principal component (Fig. 6). PC2 separates p20 and adult RAs, with RAs from p40 birds exhibiting an apparent chemical transition from p20 to adults. The P40 samples in particular show variation along PC2, intermediate between the two extremes of the P20 and adult samples. This variation is suggestive of (and may be related to) the variable progress that different individuals are making in their song development at this age (Tchernichovski et al., 2001). The corresponding loadings plot shows a relative increase in high molecular weight ions (m/z ~800–860) in the adult RA compared to the p20 RAs. Although these have not been positively identified, they may represent esterified lipids such as triglycerides and glycosphingolipids (Pernber et al. 2007, Touboul et al. 2005). In addition to higher levels of many fatty acids in adult RAs (i.e., DHA and 11-eicosenic acid), a peak previously identified as vitamin E (m/z 429) (Monroe et al. 2005) also shows relative higher levels in RAs from adult birds; in this case, however, we do not observe several characteristic SIMS fragmentation ions as previously observed. Increased vitamin E levels have been shown during development of mammalian brains (Zhang et al. 1996). Myelination in the RA has previously been identified as taking place around p50 (Clayton 1997). Therefore, we expect to see higher relative levels of phosphate-containing lipids in p20 RAs compared to adults. Other ions (m/z <150) show significant association with p20 RAs and likely represent fragmentation ions of larger molecules, making their identification difficult.
The subcellular imaging of fatty acids and other small molecules by ToF-SIMS in brain sections opens significant avenues in the study of neurochemistry and disease, especially when applied in an animal model like the zebra finch. Future studies to focus on the identification of unknown peaks in the ToF-SIMS spectra will significantly aid our understanding of small molecule heterogeneities across the zebra finch song system and their prospective biological importance in brain development and learning and memory.
We thank Timothy Spila for his assistance with the ToF-SIMS and Alexander Ulanov with the GC-MS. This investigation was supported by the National Institutes of Health (NIH) under a Ruth L. Kirschstein National Research Service Award No. F31 NS060179-01A1 to KRA, by Award No. R01 DE018866 from the National Institute of Dental and Craniofacial Research (NIDCR) and the Office of Director, NIH, and by Award No. P30 DA018310 from the National Institute On Drug Abuse (NIDA) to JVS, and Award No. PHS 2 R01 NS051820 to DFC. Research was carried out in part in the Frederick Seitz Materials Research Laboratory Central Facilities, University of Illinois at Urbana-Champaign, which are partially supported by the U.S. Department of Energy (DOE) under Award Nos. DE-FG02-07ER46453 and DE-FG02-07ER46471. This work is adapted from the doctoral dissertation (University of Illinois) of Kensey R. Amaya. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIDCR, NIDA, NIH or the DOE.
Authors report no conflict of interest.