With a rapidly aging global human population, finding a cure for late onset neurodegenerative diseases has become an urgent enterprise. However, these efforts are hindered by the lack of understanding of what constitutes the phenotype of aged human microglia—the cell type that has been strongly implicated by genetic studies in the pathogenesis of age-related neurodegenerative disease. Here, we establish the set of genes that is preferentially expressed by microglia in the aged human brain. This HuMi_Aged gene set captures a unique phenotype, which we confirm at the protein level. Furthermore, we find this gene set to be enriched in susceptibility genes for Alzheimer’s disease and multiple sclerosis, to be increased with advancing age, and to be reduced by the protective APOEε2 haplotype. APOEε4 has no effect. These findings confirm the existence of an aging-related microglial phenotype in the aged human brain and its involvement in the pathological processes associated with brain aging.
Recent genetic studies of aging-related neurodegenerative diseases have uncovered many genetic variants that appear to function predominantly through the innate immune system; these results suggest a fundamental role for myeloid cells, including microglia (the resident innate immune cells of the central nervous system) in the pathogenesis of diseases such as Alzheimer’s disease (AD)1, Parkinson’s disease (PD)1 and amyotrophic lateral sclerosis (ALS)2. However, the contribution of microglia to the pathophysiology of these diseases is notoriously difficult to study in mouse, due to the differences in age-related changes in microglial function between mice and humans3, 4. The lack of a transcriptome-wide reference profile of human microglia from aged individuals limits our understanding of the aged microglia phenotype and function in humans, particularly in advanced age. Understanding this temporal dimension is critical given that aging is the largest risk factor for late onset neurodegenerative diseases5.
In this study, we leverage two prospective cohort studies of aging with brain autopsies6, 7, a novel protocol optimized for the isolation of human microglial cells, and cDNA library construction for RNA sequencing (RNA-Seq) from small cell numbers to perform a comprehensive assessment of the transcriptomic landscape of aged human microglia and to create a resource for the community of neurodegenerative disease investigators. We establish the HuMi_Aged gene set that consists of genes primarily expressed in microglia in the aged human brain. This gene set displays many unique functional aspects that are highly relevant to brain aging. Furthermore, we show that this gene set is associated with neuropathological traits and susceptibility genes of AD, confirming the involvement of this cell type in the pathophysiology of the aging brain.
Microglia isolation and library construction
We have established an optimized pipeline for the isolation of microglia from post mortem brain samples and an RNA-Seq library construction approach that is specifically suited for use with low cell numbers (described in detail in the Methods section). Using mechanical tissue dissociation followed by magnetic bead based enrichment and fluorescence activated cell sorting (Supplementary Figure 1), this protocol yielded a microglia population, that is free of CD45 high macrophages (Supplementary Figure 2), infiltrating monocytes (Supplementary Figure 2) or other blood cells (Supplementary Figure 3). The resulting RNA-Seq dataset derives from the microglia of ten donors; all microglia were extracted from a sample of dorsolateral prefrontal cortex (DLPFC). All ten subjects had a non-zero burden of amyloid and tau pathology (a characteristic of the aged human brain; Supplementary Figure 4 and Supplementary Table 1), and three of these subjects were diagnosed with AD dementia (Supplementary Table 1).
Identification of the HuMi_Aged gene set
To define a set of genes that are primarily expressed by microglia in the aged human brain, we took advantage of existing DLPFC tissue-level RNA-Seq data8 available from an independent set of participants from the same cohorts (N = 540). By using a 4-fold increase in microglia:bulk tissue expression as a threshold, we identified 1054 microglia-enriched genes (referred to as “the HuMi_Aged gene set”; Fig. 1a and Supplementary Data 1). Among the microglia-enriched genes we found known markers of microglia (Fig. 1a); many of them in the top 100 expressed genes, confirming the validity of our approach. However, not all previously identified microglia genes were found to be microglia-enriched in our dataset. Interestingly, many genes that were microglia specific in the mouse (e.g., SALL19) were not part of the aged human microglia core transcriptomic signature.
When we compared the HuMi_Aged gene set to other recently published microglia core gene sets10, 11 we found that the HuMi_Aged microglia signature had a unique set of genes, not present in other adult10 or pediatric11 microglia signatures (Supplementary Figure 5a). Among others, pathways associated with DNA damage, telomere maintenance and phagocytosis were significantly enriched in genes that were unique to the aged human microglia signature (Supplementary Figure 5b).
Enrichment of HuMi_Aged in susceptibility genes
Using series of hypergeometric tests we found that genes in the HuMi_Aged gene set were enriched in susceptibility genes for AD (p = 4.1 × 10−5) (Fig. 1b) and multiple sclerosis (p = 0.0032) but not PD (p = 0.82), ALS (p = 0.7) or schizophrenia (p = 0.83) (Supplementary Figure 6), as defined by the NHGRI-EBI catalog. Nonetheless, a subset of PD (e.g., SLC50A1), ALS (ITPR2), and schizophrenia (RENBP) susceptibility genes were part of the microglia signature in the aged human brain. Interestingly, RENBP was not found to be expressed in microglia from middle aged brains12. Our findings therefore reinforce the earlier notion, that within the brain, a significant amount of the genetic load that influences the onset of certain neurodegenerative diseases may exert its function through microglia. Focusing on late onset AD (LOAD), we found that many well-known susceptibility genes (CD33, INPP5D, MS4A4A, SORL1, and TREM2) are part of the HuMi-Aged gene set, while others, such as SPI113, were not. We also identified additional susceptibility genes not known to function in microglia in the context of neurodegeneration (e.g., SCIMP, SPPL2A14).
Relationship of the HuMi_Aged to traits and genotypes
We took advantage of the large sample size of the bulk DLPFC RNAseq dataset (N = 540) and examined how our HuMi_Aged signature behaved in that tissue-level dataset with respect to traits available in our cohort. For these analyses we created a meta-feature for the HuMi_Aged gene set that resulted in a single value for each participant (Supplementary Data 2). The association of this meta feature was investigated using linear regression. Interestingly, the expression level of the HuMi_Aged gene set in the frontal cortex of the participants increased with advancing age at death (p = 0.0012, Table 1), suggesting that the proportion of microglia in the DLPFC may increase with age or that microglia increase the expression of this transcriptional program over time. However, the aged microglia signature is not associated with a diagnosis of AD dementia or a global measure of AD pathology in these tissue-level data; nonetheless, there is a suggestion that it may relate to amyloid deposition (p = 0.011). These associations do not change when we perform stratified analyses in subjects with and without a clinical diagnosis of AD (Supplementary Data 3). At the individual gene level, a small number of genes in these ten participants were found to be associated with neuritic plaques (NP), diffuse plaques, and neurofibrillary tangles (NFT) after correction for multiple testing. These genes will require further validation given the modest sample size (N = 10) of the present study (Supplementary Figure 7).
From a genetic point of view, the APOE haplotype is associated with the HuMi_Aged meta-feature (p = 0.0088), and, interestingly, the effect appears to be driven not by APOE ε4 but by APOE ε2, the haplotype that is protective for AD. In our tissue-level data, APOE ε2 was associated with reduced expression of HuMi_Aged (Fig. 1c) (p = 0.0064), consistent with the predicted direction of effect.
Identification of human microglia genes affected by aging
In order to identify the microglia genes that are affected by aging in the human cortex, we took advantage of another published adult human microglia transcriptomic dataset, that is derived from middle aged individuals12. We performed an exploratory study comparing the transcriptomic profiles of middle aged (mean age = 53, SD = ±5.29, N = 3) and our aged (mean age = 94.07, SD = ±0.95, N = 10) human microglia (Supplementary Figure 8a). By assessing only those genes that were reliably detected in both datasets (Supplementary Figure 8b; Materials and Methods), we identified 1060 genes that were up-regulated (logFC > 2, adjusted p-value > 0.05), and 1174 genes that were down-regulated in our aged human microglia (Fig. 2a, Supplementary Data 4). Importantly, both datasets were highly enriched in microglia genes (Supplementary Figure 8c). Intriguingly, gene set enrichment analysis (GSEA) of the differentially expressed genes identified the Amyloid fiber formation (Fig. 2b) REACTOME gene set to be enriched for genes that are up-regulated in aged human microglia, while the TGFβ signaling KEGG pathway (Fig. 2c) was enriched for down-regulated genes. These results suggest that human microglial aging may result both in gain of function as well as in loss of function of certain transcriptional programs; diminished TGFβ signaling highlights the perturbation of homeostatic programs as microglia activate reactive pathways to respond to aging-related changes such as the accumulation of amyloid pathology.
The proteome of aged human microglia
To assess whether our transcriptomic approach faithfully captured genes that were expressed at the protein level in microglia and could therefore affect cellular function, we also generated a proteomic profile from one sample of 5000 purified microglia isolated with the same pipeline that was used to produce the RNAseq dataset. Using LC-MS mass spectrometry, we generated a shotgun proteomic profile consisting of 640 proteins for which we have a measure of relative expression. As expected, the detected proteins were distributed along the gene expression spectrum, with a skew towards the more abundant gene transcripts (Supplementary Figure 9a). By comparing the expression levels of proteins and mRNA, we found that these two measures were considerably correlated (rS = 0.3112, p < 0.0001) (Supplementary Figure 9b). Twenty seven of the detected proteins were also part of HuMi_Aged gene set. Gene ontology analysis of the detected proteins revealed some of the same REACTOME pathways that we found to be up-regulated in the aged human microglia transcriptome, such as the ER-Phagosome pathway (FDR = 3.19E-14) (Fig. 2d, e). The list of proteins detected in aged human microglia is available in Supplementary Data 5.
Here, we present a novel microglia isolation protocol and RNA-Seq library construction approach to create transcriptomic profiles from autopsy-derived microglia using only 5000 cells per individual. This number has been previously empirically established in our laboratory to be the lowest cell number at which the stochastic drift in population mean is no longer substantial. Given that current transcriptomic approaches require hundreds of thousands of microglia cells10, 11 and the availability of fresh autopsy samples from well-characterized subjects is very limited, the protocol presented here will be a useful tool for the scientific community in order to most efficiently utilize the available precious human brain specimens, especially in the case of samples where viability is compromised, such as those affected by chronic neurodegeneration and/or aging. Furthermore, we provide the scientific community with the first transcriptomic atlas of aged human microglia (publicly available at http://shiny.maths.usyd.edu.au/Ellis/MicrogliaPlots website). This RNA-Sequencing dataset is derived from quasi-centenarian donors of the ROS and MAP cohorts.
It was beyond the scope of this study to discriminate between microglia-derived macrophages and infiltrating monocyte-derived macrophages, primarily due to the current lack of markers that would reliably allow us to make that distinction in human samples. Nonetheless, the lack of a CD45high subpopulation in our preparations further supports that our microglia preparations are largely devoid of blood-borne monocytes and perivascular macrophages, both of which would have shown up on the scatter plots as a small CD11b+/CD45high subpopulation on top of the CD11b+/CD45+ microglia population. Furthermore, the high expression of the microglia specific genes (many of whose expression was close to the 100th percentile) confirms that blood borne monocyte contamination was negligible; the lack of considerable CCR2 expression in our dataset shows that our preparations were also free from recently recruited tissue infiltrating inflammatory monocytes.
By combining our microglia transcriptomic profiles with existing cortical RNAseq data from an independent set of subjects from the same cohort, we derived the HuMi_Aged gene set and have illustrated the utility of this resource by showing that it captures an important fraction of genetic susceptibility to both AD and MS. In particular, we report the intriguing result that the APOEε2 haplotype is associated with a reduced HuMi_Aged signature, consistent with its role as a protective factor in AD, and this observation aligns with recent reports that APOE may interact with microglial genes such as TREM215,16,17. APOEε4 is a much stronger risk factor for AD but does not appear to be related to this microglial signature and most likely exerts its effect through another mechanism.
Importantly, we also found that the HuMi_Aged core microglia profile displayed a number of differences in relation to the already available pediatric and adult microglia signatures. Functional annotation of the genes that were unique to the aged human microglia signature presented here revealed that cellular and organismal aging related pathways and biological processes were primarily affected. These findings confirm the notion, that the aged human brain harbors a distinctive microglia phenotype, whose identity is shaped by cell autonomous/intrinsic (DNA damage response, telomere maintenance) as well as extrinsic (decline in homeostatic and increase in phagocytic signaling from the brain parenchyma) factors that are unique to the aging brain environment.
Thus, the HuMi_Aged gene set can be used to more accurately explore the role of microglia in other tissue-level datasets from older brains. Increasing our sample size will allow us to more directly dissect the contribution of microglia to brain aging and neurodegenerative diseases as current tissue level profiles probably under-estimate the contribution of microglia which makes up a small proportion of the tissue and often have relatively small amounts of RNA. Nonetheless, this resource will be a critical reference for efforts to optimize in vitro systems (using either monocytes18 or induced pluripotent stem cell-derived microglial like cells19,20,21) for neurodegenerative disease studies. Finally, our initial proteomic profile not only validates our transcriptomic data but also presents a number of proteins that could be targets for developing novel markers of human microglia in histological studies and for the development of new PET ligands with which to assess the immunologic state of the aged human brain.
Cohorts and donors
The biological specimens used in this study originated from two prospective studies of aging: the Religious Orders Study (ROS)6 and the Memory and Aging Project (MAP)7. Participants have to be at least 53 (ROS) or 55 (MAP) years old and non-demented at enrollment and sign an Anatomical Gift Act agreeing to donate their brain and spinal cord at the time of death. Thus, they represent a sample of the older population from the Chicago, IL metropolitan area. Each subject undergoes annual neuropsychologic evaluations while alive and a structured, quantitative neuropathologic examination at autopsy. All brain autopsies, experiments, and data analysis were done in compliance with protocols approved by the Partners Human Research Committee and the Rush University Institutional Review Board. The data presented in this study originates from ten donors. The clinicopathological characteristics of the participants are shown in Supplementary Table 1. Their mean age at death was 95 years and 80% of them were female. Nine out of ten of the participants showed a range of amyloid and tau pathology accumulation that is typical in this type of older, population-based sample. Three of the donors were ante mortem diagnosed with clinical AD.
Brain autopsy and shipping of brain specimens
To obtain the midfrontal gyrus (BA 9/46) a 1.5 cm × 1.5 cm thick section is cut off from the first cerebral slab anterior to the caudate. After weighing, the tissue is placed in ice-cold transportation medium (Hibernate-A medium (Gibco, A1247501) containing 1% B27 serum-free supplement (Gibco, 17504044) and 1% GlutaMax (Gibco, 35050061)) and shipped overnight at 4 °C with priority shipping. Brain specimens were distributed for this project from autopsies taking place Sunday morning to Thursday. Only autopsies for which the post mortem delay was less than 12 h were included in this study.
Microglia isolation and sorting
Upon arrival of the autopsy brain sample, the cerebral cortex and the underlying white matter were dissected under a stereomicroscope. All procedures were performed on ice. Only microglia isolated from the grey matter were used in this study. The dissected tissue was placed in HBSS (Lonza, 10-508F) and weighed. Subsequently the tissue was homogenized in a 15 ml glass tissue grinder—0.5 g at a time. The resulting homogenate was filtered through a 70 μm filter and spun down with 300 g for 10 min. The pellet was resuspended in 2 ml staining buffer (PBS (Lonza, 17-516F) containing 1% FBS) per 0.5 g of initial tissue and incubated with anti-myelin magnetic beads (Miltenyi, 130-096-733) for 15 min according to the manufacturers specification. The homogenate was than washed once with staining buffer and the myelin was depleted using Miltenyi large separation columns. The cell suspension was spun down and incubated with anti-CD11b magnetic beads (Miltenyi, 130-049-601, clone M1/70) for 15 min. Following a wash with staining buffer the CD11b+ cells were isolated on a Miltenyi MS column while the CD11b− fraction was cryopreserved using FBS containing 10% DMSO. The CD11b positive fraction was than incubated with anti-CD11b AlexaFluor488 (BioLegend, 301318, clone ICRF44) and anti-CD45 AlexaFluor647 (BioLegend, 304018, clone HI30) antibodies as well as 7AAD (BD Pharmingen, 559925) for 20 min on ice. Subsequently the cell suspension is washed twice with staining buffer, filtered through a 70 μm filter and the CD11b+/CD45+/7AAD− cells (Supplementary Figure 2b) were sorted on a BD FACS Aria II sorter. Cells were sorted in A1 well of a 96 well PCR plate (Eppendorf, 951020401) containing 25 μl of TCL buffer (Qiagen, 1031576) with 1% beta mercaptoethanol (Sigma, M3148). Following FACS the lysate was vigorously vortexed for 30 s, spun down, snap frozen on dry ice and stored at −80 °C until further processing.
Library construction and sequencing
Library construction was performed using the SmartSeq-2 protocol described in detail elsewhere22 with minor modifications. Briefly, the 96 well plates (Eppendorf, 951020401) were thawed on ice and spun down. RNA Isolation. 2.2 × volume of RNA-SPRI (Beckman Coulter, A63987) beads were added to the cell lysate, mixed, incubated for 10 min at room temperature and placed on a magnet (Thermo Fischer, 12027) for 5 min. The supernatant was removed and the beads were washed with 80% ethanol (VWR, 89125-170) three times, let to dry on air for 10 min on the magnet and subsequently resuspended in Master Mix 1 (containing RT primers 10 μM (IDT—Custom, sequence below), dNTP mix 10 mM (Thermo-Fischer, R0192) and RNase-inhibitor 4 U/μl (Clontech, 2313B) in water). The plate is then incubated at 72 °C for 3 min in a thermocycler and then placed on ice. Whole Transcriptome Amplification. Subsequently the beads are dispersed in Master Mix 2 (containing Maxima Buffer (Thermo-Fischer, EP0753), betaine 5M (Sigma-Aldrich, B0300-1VL), MgCl2 10 mM (Sigma-Aldrich, M1028), TSO 10 μM (Exiqon Custom, sequence below), RNase inhibitor 40 U/μl, Maxima RNaseH-minus RT 200 U/μl in water) and a PCR run is performed on the thermocycle with the following parameters: Hold (42 °C, 90 min), 10 cycles (50 °C, 2 min; 42 °C, 2 min), Hold (70 °C, 15 min). PCR Preamplification. The plate is then removed from the thermocycle, Master Mix 3 (containing ISPCR primer 10 μM (IDT custom, sequence below) KAPA HiFi HotStart ReadyMix (KAPA BioSystems, KK2602) in water) is added, and run again with the following parameters: Hold (98 °C, 3 min), 14 cycles (98 °C, 15 s; 67 °C, 20 s; 72 °C, 6 min), Hold (72 °C, 5 min). DNA Cleanup. The PCR products were purified with 0.8 × AMPure XP SPRI beads (Beckman Coulter, A63880). The AMPure XP SPRI beads were added to the sample, mixed thoroughly, incubated at room temperature for 6 min and placed on the magnet for 6 min. The supernatant was pipetted off and the beads were washed with 70% ethanol 2 times and than let to dry on room temperature for 10 min. The material was eluted from the beads in TE (TEKNOVA, T0228), removed the beads from the eluent with a magnet and the eluent was than transferred to a new 96 well PCR plate for a second round of PCR product purification with AMPure XP SPRI beads. Quality control. The quality and the quantity of the cDNA were assessed with Qubit DNA HS (Life Technologies, Q32854) and BioAnalyzer DNA HS assays (Agilent, 5067-4626). Library construction. All samples were diluted to the concentration range of 0.1–0.2 ng/μl in order to be used with the Nextera XT kit (Illumina, FC-131-1096) for library construction. In a fresh plate TD, ATM and the input sample were mixed and than placed in a thermocycler for the following program: Hold (55 °C, 10 min), Hold (10 °C, ∞); following which it is placed on ice. Subsequently NT, NPM, and mixed indices were added to the samples and the plate was run using the following parameters: Hold (72 °C, 3 min), Hold (95 °C, 30 s), 12 cycles: (95 °C, 10 s; 55 °C, 30 s; 72 °C, 60 s), Hold (72 °C, 5 min), Hold (4 °C, ∞). Sample cleanup. Subsequently the samples were pooled and DNA cleanup was performed by adding 0.9 × volume of AMPure XP SPRI beads, incubating for 5 min on room temperature, placing the sample on a magnet for 5 min, washing the beads twice with 80% ethanol and then eluting the cDNA with TE. The cleanup step is repeated once. Quality control. The quality and the quantity of the cDNA were assessed with Qubit DNA HS and BioAnalyzer DNA HS assays. Sequencing. The pool of ten samples was sequenced on one lane of an Illumina HiSeq2500 flowcell with a read length of 100 bp and paired end reads.
Quality control and data processing of RNA-Seq data
RNA-Seq reads in FASTQ format were inspected using FASTQC program. Barcode and adapter contamination, low quality regions (10 bp at beginning of each fastq reads) were trimmed using FASTX-toolkit. We then used Tophat (2.1.0) to align trimmed reads to human reference genome sequences (hg19) and transcript annotation from Gencode (v19) then applied Cufflinks (2.2.1) to estimate gene and isoform abundance. The estimation of abundance is in FPKM format. We then performed the following normalization approach: first, we filtered out low expressed genes with FPKM < 0.1 in more than two samples, resulting in expression levels for 9489 genes. Then we used voom method in limma23 package to normalize filtered FPKM values.
Identification of microglia enriched genes
Given that microglia constitute only 12% of the cells in the prefrontal cortex and are known to have very low RNA content, our argument was that genes that will be significantly highly expressed in the isolated microglia samples, when compared to the bulk, will be most likely primarily expressed by microglia. To make the microglia and bulk samples more comparable the mapped genes were first filtered to only include those with a uniprot identifier. Further normalization was then performed, by comparing the log gene expression of a sample to the average of all samples, a robust linear model was used to normalize out any residual GC content and gene length artifacts. Then, by contrasting the bulk RNA-Seq data with the gene expression profiles of isolated microglia and using a fold change cut off of 4, we identified 1054 genes that were enriched in microglia (Fig. 1a; FC genes in Supplementary Data 1). Seven hundred seventy one genes reached statistical significance (PVAL genes; Supplementary Data 1). Statistical significance depends on the variability between samples, and in our case, this might originate from the microglial responses to pathological features present in the brains of the donors, that had varying amounts of amyloid load and tau pathology (Supplementary Table 1). In order not to exclude the genes that are responsive to the aging brain environment, we decided to use the FC genes for downstream analysis.
The enrichment of the HuMi_Aged gene set in genes associated with neurodegenerative disease and psychiatric disorders was tested with an over-representation analysis. Genes that had previously been associated with neurodegenerative disease and psychiatric disorders were sourced from the NHGRI-EBI Catalog of published genome-wide association studies24.
Association with traits
A meta-feature was created to capture the change in expression of the HuMi_Aged gene set as a collective in the bulk tissue and assess its association with various AD an aging associated traits. To do this each gene was standardized to have variance equal to 1 and then the expression of all genes in the HuMi_Aged gene set was averaged over each sample. A series of t-tests were then used to test for association of the meta-feature with various clinical, pathological and mutation variables.
Differential gene expression
We contrasted the gene expression levels of aged human microglia with a previously published microglia transcriptomic dataset derived from middle-aged individuals (NCBI GEO accession number: GSE73721)12. The differential gene expression analysis was performed using limma package23. We identified 2234 genes (logFC > 2 and logFC<−2, adjusted p-value < 0.05, Supplementary Data 4) that were differentially expressed in aged human microglia.
GSEA and pathway analysis
For proteomic analysis microglia were isolated as described above. 5000 CD11b+/CD45+/7AAD- cells were sorted in A1 well of a 96 well plate containing 100 μl of PBS. Following FACS the cells were spun down after which all but 10 μl of PBS was removed from A1 well and the plate was than snap frozen on dry ice and stored at −80 °C until further processing. Sorted cell pellets were lysed and extracted by adding 10 μL of homogenization buffer (8 M urea, 10 mM dithiothreitol, 50 mM Tris pH = 8) followed by 30 s in a bath sonicator. The lysate was then incubated at 37 °C for 30 min to denature and reduce the proteins. Protein solution was quantitatively transferred to a low retention LC vial (Waters) using 20 μL of 50 mM Tris pH = 8. SNaPP analysis was carried out as described previously26, 27. Briefly, 25 μL of sample was injected onto a 150 µm × 2 cm immobilized enzyme reactor for digestion. Following digestion, peptides were separated using a 180 min gradient on an in-house 50 µm × 75 cm C18 (Phenomenex) analytical column. The SNaPP system was coupled to an Orbitrap Fusion Lumos mass spectrometer (Thermo Scientific) operated in top speed mode. Fragmentation was carried out in the ion trap with maximum injection time of 250 ms for MS2 to increase sensitivity for low intensity ions. The label-free data was quantified using the iBAQ (intensity based absolute quantification) approach28.
Immunohistochemistry was performed as described elsewhere29. Briefly brains were removed and processed according to a standard protocol. One hemisphere was cut coronally into 1 cm slabs and fixed in 4% paraformaldehyde. β-amyloid deposits and PHFtau tangles were assessed in 20 µm sections. Immunohistochemistry and computer-assisted image analysis were used for β-amyloid (clone 4G8, 1:9000 Covance Labs, Madison, WI) and stereology was used for PHFtau tangles (clone AT8, 1:2000; ThermoScientific, Waltham, MA) across eight different brain regions including the entorhinal cortex, the hippocampus at CA1, superior frontal cortex (Broadmann area [BA] 6/8), mid frontal cortex (BA 46/9), inferior temporal cortex (BA 20), angular gyrus cortex (BA 39/40), cingulate gyrus (BA 32/33) and calcarine cortex (BA 17). β-amyloid load and the density of PHFtau tangle density was obtained by averaging the mean percentage area per region, across all regions. The absence of β-amyloid was characterized by a β-amyloid load of zero in all the eight immunostained sections. NP and NFT were identified with modified Bielshowsky stain in 6 µm sections in five different regions (entorhinal cortex, hippocampus at CA1, midfrontal cortex, middle temporal gyrus, and inferior parietal cortex). CERAD criteria assessed NP burden and a Braak staging assessed the distribution and severity of NFT pathology. The diagnosis of pathologic AD was based on the National Institute on Aging (NIA)–Reagan criteria (1997).
Since the brain tissue is obtained at autopsy with a postmortem delay of, on average, 7 h, the release of surviving monocytes from the clotted blood present in the blood vessels of the brain, with the non-enzymatic approach used in this study, is exceedingly unlikely. The high expression of the markers previously reported to be microglia specific when compared to monocytes (e.g., P2RY12, TMEM119, TREM2, GPR34, CX3CR1)30,31,32 in our preparations (Fig. 1a and Supplementary Figure 8c) further supports this scenario. The lack of CD11b−/CD45+ cells on the flow cytometry scatter plots (Supplementary Figure 2b) further supports the idea, that there was no blood borne immune cell contamination in our preparations. Nonetheless, it was beyond the scope of this study to discriminate between microglia derived macrophages and infiltrating monocyte derived macrophages, primarily due to the current lack of technologies that would reliably allow us to make that distinction in human samples. Despite the differences in the mode of isolation (CD11b/CD45 based FACS versus CD45 based immunopanning), there was an almost perfect overlap between the Zhang and our dataset in terms of the expression levels of previously established microglia marker genes, since in both datasets they scored close to the 100th percentile (Supplementary Figure 8c). This increases our confidence that the observed differences in gene expression are, with some contribution from potential regional and disease specific differences, primarily due to organismal aging and/or cellular senescence.
The RNA-Sequencing data originating from the bulk dorsolateral prefrontal cortex (DLPFC; 540 donors) and from purified microglia (10 donors) from the same brain region is available at Synapse (https://www.synapse.org/#!Synapse:syn3219045 and syn11468526). The microglia RNA-Sequencing dataset is also available and searchable at http://shiny.maths.usyd.edu.au/Ellis/MicrogliaPlots/. Please note, that the searchable platform will ultimately move to the website of the Center for Translational and Computational Neuroimmunology (at Columbia University Medical Center, New York), which is currently under development. For all other inquires please contact the corresponding authors.
Raj, T. et al. Polarization of the effects of autoimmune and neurodegenerative risk alleles in leukocytes. Science 344, 519–523 (2014).
Cooper-Knock, J. et al. A data-driven approach links microglia to pathology and prognosis in amyotrophic lateral sclerosis. Acta Neuropathol. Commun. 5, 23 (2017).
Streit, W. J. & Xue, Q. S. The Brain’s Aging Immune System. Aging Dis. 1, 254–261 (2010).
Smith, A. M. & Dragunow, M. The human side of microglia. Trends Neurosci. 37, 125–135 (2014).
Wyss-Coray, T. Ageing, neurodegeneration and brain rejuvenation. Nature 539, 180–186 (2016).
Bennett, D. A., Schneider, J. A., Arvanitakis, Z. & Wilson, R. S. Overview and findings from the religious orders study. Curr. Alzheimer Res. 9, 628–645 (2012).
Bennett, D. A. et al. Overview and findings from the rush Memory and Aging Project. Curr. Alzheimer Res. 9, 646–663 (2012).
Lim, A. S. et al. Sex difference in daily rhythms of clock gene expression in the aged human cerebral cortex. J. Biol. Rhythms 28, 117–129 (2013).
Buttgereit, A. et al. Sall1 is a transcriptional regulator defining microglia identity and function. Nat. Immunol. 17, 1397–1406 (2016).
Galatro, T. F. et al. Transcriptomic analysis of purified human cortical microglia reveals age-associated changes. Nat. Neurosci. 20, 1162–1171 (2017).
Gosselin, D. et al. An environment-dependent transcriptional network specifies human microglia identity. Science 356, 1248–1259 (2017).
Zhang, Y. et al. Purification and characterization of progenitor and mature human astrocytes reveals transcriptional and functional differences with mouse. Neuron 89, 37–53 (2016).
Huang, K. L. et al. A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer’s disease. Nat. Neurosci. 20, 1052–1061 (2017).
Liu, J. Z., Erlich, Y. & Pickrell, J. K. Case-control association mapping by proxy using family history of disease. Nat. Genet. 49, 325–331 (2017).
Yeh, F. L., Wang, Y., Tom, I., Gonzalez, L. C. & Sheng, M. TREM2 binds to apolipoproteins, including APOE and CLU/APOJ, and thereby facilitates uptake of amyloid-beta by microglia. Neuron 91, 328–340 (2016).
Atagi, Y. et al. Apolipoprotein E is a ligand for triggering receptor expressed on myeloid cells 2 (TREM2). J. Biol. Chem. 290, 26043–26050 (2015).
Bailey, C. C., DeVaux, L. B. & Farzan, M. The triggering receptor expressed on myeloid cells 2 binds apolipoprotein E. J. Biol. Chem. 290, 26033–26042 (2015).
Ryan K. J. et al. A human microglia-like cellular model for assessing the effects of neurodegenerative disease gene variants. Sci. Transl. Med. 9, eaai7635 (2017).
Pandya, H. et al. Differentiation of human and murine induced pluripotent stem cells to microglia-like cells. Nat. Neurosci. 20, 753–759 (2017).
Muffat, J. et al. Efficient derivation of microglia-like cells from human pluripotent stem cells. Nat. Med. 22, 1358–1367 (2016).
Abud, E. M. et al. iPSC-derived human microglia-like cells to study neurological diseases. Neuron 94, 278–293 (2017).
Picelli, S. et al. Full-length RNA-seq from single cells using Smart-seq2. Nat. Protoc. 9, 171–181 (2014).
Law, C. W., Chen, Y., Shi, W. & Smyth, G. K. voom: precision weights unlock linear model analysis tools for RNA-seq read counts. Genome Biol. 15, R29 (2014).
MacArthur, J. et al. The new NHGRI-EBI catalog of published genome-wide association studies (GWAS Catalog). Nucleic Acids Res. 45, D896–D901 (2017).
Subramanian, A. et al. Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles. Proc. Natl Acad. Sci. USA 102, 15545–15550 (2005).
Clair, G. et al. Spatially-resolved proteomics: rapid quantitative analysis of laser capture microdissected alveolar tissue samples. Sci. Rep. 6, 39223 (2016).
Huang, E. L. et al. SNaPP: simplified nanoproteomics platform for reproducible global proteomic analysis of nanogram protein quantities. Endocrinology 157, 1307–1314 (2016).
Wilhelm, M. et al. Mass-spectrometry-based draft of the human proteome. Nature 509, 582–587 (2014).
Farfel, J. M., Yu, L., De Jager, P. L., Schneider, J. A. & Bennett, D. A. Association of APOE with tau-tangle pathology with and without beta-amyloid. Neurobiol. Aging 37, 19–25 (2016).
Hickman, S. E. et al. The microglial sensome revealed by direct RNA sequencing. Nat. Neurosci. 16, 1896–1905 (2013).
Chiu, I. M. et al. A neurodegeneration-specific gene-expression signature of acutely isolated microglia from an amyotrophic lateral sclerosis mouse model. Cell Rep. 4, 385–401 (2013).
Butovsky, O. et al. Identification of a unique TGF-beta-dependent molecular and functional signature in microglia. Nat. Neurosci. 17, 131–143 (2014).
We would like to express our gratitude to the participants of the ROS and MAP studies and their families. This work was supported by US National Institutes of Health (grants AG010161, AG017917, AG043617, NS089674, AG046152, AG048015, and AG036836) and the Illinois Department of Public Health. M.O. is a recipient of the Alzheimer’s Association Research Fellowship Award.
The authors declare no competing financial interests.
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Olah, M., Patrick, E., Villani, A. et al. A transcriptomic atlas of aged human microglia. Nat Commun 9, 539 (2018) doi:10.1038/s41467-018-02926-5
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