Metastasis of melanoma significantly worsens prognosis; thus, therapeutic interventions that prevent metastasis could improve patient outcomes. Here, we show using humanized mice that colonization of distant visceral organs with melanoma is dependent upon a human CD33+CD11b+CD117+ progenitor cell subset comprising <4% of the human CD45+ leukocytes. Metastatic tumor-infiltrating CD33+ cells from patients and humanized (h)NSG-SGM3 mice showed converging transcriptional profiles. Single-cell RNA-seq analysis identified a gene signature of a KIT/CD117–expressing CD33+ subset that correlated with decreased overall survival in a TCGA melanoma cohort. Thus, human CD33+CD11b+CD117+ myeloid cells represent a novel candidate biomarker as well as a therapeutic target for metastatic melanoma.
Mechanisms sustaining the growth of human melanoma in distant organs remain poorly defined. This is important because metastatic dissemination remains a major clinical challenge (Eggermont et al., 2016). Melanoma can metastasize to all organs (Gupta and Brasfield, 1964; Einhorn et al., 1974; Meyer and Stolbach, 1978; Nathanson et al., 1967; Patel et al., 1978), and patients with nonpulmonary visceral metastasis, including liver, have the worst prognosis (Balch et al., 2009). Improved survival has been documented for patients with metastatic melanoma treated with B-raf proto-oncogene serine/threonine kinase– and/or mitogen-activated protein kinase kinase–targeted therapies (Flaherty et al., 2016; Long et al., 2017) or with blocking antibodies targeting CTL-associated protein (CTLA)-4 (Hodi et al., 2010) and/or programmed death (PD)-1 (Wolchok et al., 2017). However, a significant fraction of patients do not achieve prolonged survival even in combination therapy trials and succumb to treatment-resistant metastatic disease (Wolchok et al., 2017).
Dissemination and growth in distant organs are driven by a complex interplay between cancer cells and their microenvironment. A number of cell types of myeloid lineage have been implicated in cancer metastasis (Garner and de Visser, 2020). In the mouse, neutrophils are engaged in various steps of metastasis (Jaillon et al., 2020), including support of cancer cell proliferation and survival (Acharyya et al., 2012; Ouzounova et al., 2017; Szczerba et al., 2019), angiogenesis (Bekes et al., 2011; Nozawa et al., 2006), increased extravasation of disseminated cancer cells (Spiegel et al., 2016), and inhibition of natural killer (NK) cell– and CTL-mediated cancer cell clearance (Coffelt et al., 2015; Spiegel et al., 2016). Immature myeloid cells that have not completed differentiation and are able to exert suppressive effects on adaptive immunity (i.e., myeloid-derived suppressor cells) promote invasion, angiogenesis, and metastasis formation (Datta et al., 2019). Furthermore, tumor-associated macrophages promote development of metastatic disease by means of supporting tumor growth in target tissues and escape from NK and T cells (Etzerodt et al., 2019; Lewis et al., 2016; Mantovani et al., 2017; Ruffell and Coussens, 2015). Thus, myeloid cells could serve as putative therapeutic targets. Their remarkable heterogeneity makes an in-depth characterization a major goal, where in vivo studies would be most informative. However, differences in myeloid cells and their downstream signaling pathways between humans and mice (Hagai et al., 2018; Kanazawa, 2007; Mestas and Hughes, 2004; Williams et al., 2010) make it uncertain to directly extrapolate mouse in vivo data into humans. Here, using a transplantable model of human melanoma in humanized mice, we find that CD117+CD11b+CD33+ myeloid cells support melanoma growth in distant organs.
Results and discussion
Metastatic melanoma tumors in patients and in humanized mice are infiltrated with CD33+ myeloid cells
To define the landscape of leukocytes in metastatic melanoma, we analyzed transcriptional profiles of metastatic melanoma tumors from 14 patients with RNA sequencing (RNA-seq; Table S1). CIBERSORT, which estimates the fraction of various leukocyte RNA (Newman et al., 2015), revealed that nearly half of the leukocyte transcripts originated from myeloid cells (Fig. 1 A). Modular analysis (Banchereau et al., 2016) revealed several lymphoid modules including B cells (36 genes), T cells (107 genes), and cytotoxic/NK cells (59 genes) as well as IFN modules (138 genes), which together clustered patient samples into two groups (hot and cold tumors; Fig. 1 B and Table S2). Inflammation (876 genes) and myeloid (78 genes) modules were spread across all samples (Fig. 1 B). These findings were confirmed using The Cancer Genome Atlas (TCGA) melanoma cohort (Cancer Genome Atlas Network, 2015) from primary (n = 66) and metastatic (n = 264) melanoma tumors from different patients (Fig. S1 A). There, CIBERSORT revealed significantly higher monocyte/macrophage–related transcripts in metastatic versus primary tumors (Fig. 1 C). Metastatic sites also showed a significantly higher expression of pan-myeloid marker CD33 (sialic acid binding Ig-like lectin 3; P = 2.3e-07; Fig. 1 D). Immunofluorescence staining revealed the presence of CD33+ myeloid cells in close proximity to melanoma cells in patient tumors (Fig. S1 B).
To study the in vivo impact of human CD33+ (hCD33+) myeloid cells on human melanoma, we turned to nonobese diabetic/severe combined immunodeficient-γ (NSG) mice with transgenic expression of the human hematopoietic cytokines stem cell factor (SCF), GM-CSF, and IL-3 (NSG–SCF GM-CSF IL-3 [SGM3] mice) transplanted with hCD34+ hematopoietic progenitor cells (HPCs), which support the development of hCD33+ myeloid cells (Fig. S1 C, Table S3, and Table S4; Billerbeck et al., 2011). FACS analysis of hCD33+ cells from bone marrow, liver, and spleen at 12 wk after hCD34+ HPC transplant using CD11b, CD11c, CD14, CD16, CD66b, CD117, CD127, HLA-DR, and FCER1A markers (Fig. 1, E and F; and Fig. S1, D and E) revealed the qualitative and quantitative differences between humanized (h)NSG and hNSG-SGM3 mice, the latter ones displaying monocytes, granulocytes, and mast cells (Fig. S1 F). The transcriptional profiles of bulk hCD33+ cells from the spleen and liver of hNSG and hNSG-SGM3 mice at 12 wk after hCD34+ HPC transplant confirmed the phenotypic divergence between the two strains (Fig. 1 G and Table S5), with granulocyte adhesion and diapedesis and Th2 cell pathways significantly enriched in hCD33+ cells from hNSG-SGM3 mice (Fig. 1 H).
hNSG-SGM3 mice support distant organ colonization with melanoma
We then implanted the two humanized mouse strains with 107 Me275 human melanoma cells s.c. (Fig. 2 A; Rongvaux et al., 2014). Upon necropsy before any tumor-induced mortality, hNSG-SGM3 mice displayed a vastly greater number of macroscopic tumors in the spleen and liver than hNSG mice (Fig. 2 B; and Fig. S2, A–C), while implantation site s.c. tumors (primary tumors) grew at similar rates in both strains (Fig. 2 C). Immunofluorescence staining for melanoma-associated proteins, melanoma antigen recognized by T cells 1 (MART-1), and glycoprotein 100 (gp100) confirmed the presence of melanoma cells and tumor formation in distant visceral organs (Fig. 2 D and Fig. S2 D). Tumors were imaged in vivo or ex vivo with an in vivo imaging system (IVIS) to detect luciferase-labeled Me275 cells (Fig. 2, E and F). Luciferase signal was present in multiple visceral organs (liver, spleen, pancreas, stomach, kidney, lungs, and bone; Fig. 2 E). Kinetic experiments following the appearance of macroscopic tumors as well as luminescence signal reflecting tumor growth in vivo revealed that Me275 cells require at least 42 d for visceral tumors to appear (Fig. 2, F and G).
To determine if human leukocytes were involved, we compared Me275 tumor growth in NSG-SGM3 mice with or without a human immune system. Only sporadic macroscopic tumors in visceral organs could be found upon necropsy (Fig. 2 H), and no MART-1/gp-100 staining could be detected in the liver harvested from nonhumanized mice (Fig. 2 I). In contrast, distant organs were colonized with Me275 cells in hNSG-SGM3 mice (Fig. 2, H and I). In both cases, Me275 cells grew at the primary site at similar kinetics (Fig. S2 E). Thus, human leukocytes are critical for distant organ colonization by melanoma cells. This was further confirmed by adoptive cell transfer (ACT) experiments where hCD45+ leukocytes were purified from the liver and spleen of tumor-naive hNSG-SGM3 mice and adoptively transferred (107 cells) into nonirradiated tumor-naive nonhumanized NSG-SGM3 mice or NSG mice. Both cohorts were implanted with Me275 cells s.c. immediately thereafter (Fig. 2 J). NSG-SGM3 mice adoptively transferred with hCD45+ leukocytes showed significantly higher numbers of melanoma tumors in the liver than controls without ACT (Fig. 2 K). In contrast, NSG mice adoptively transferred with hCD45+ cells purified from hNSG-SGM3 mice developed only sporadic liver tumors (Fig. 2 K). Thus, the capacity of hCD45+ leukocytes to support melanoma growth in distant organs is dependent on at least one of the host human cytokines SCF, GM-CSF, and/or IL-3.
Distant organ colonization is dependent upon hCD33+ myeloid cells
Tissue examination revealed close proximity of hCD33+ cells and melanoma cells in the liver and spleen of hNSG-SGM3 mice (Fig. 3 A). The transcriptional profiles of hCD33+ cells purified from the spleen and liver of hNSG-SGM3 mice were established using RNA-seq, and the analysis was focused on the myeloid gene set selected by Nanostring. The Venn diagram analysis revealed a 78% overlap in myeloid gene expression between melanoma metastases from patients and hCD33+ cells from mice (Fig. 3 B). The top networks were driven by the expression of STAT3, STAT1, and NFKB1, identical to those observed in melanoma patients (Fig. 3 C, Fig. S2 F, Table S6, and Table S7). To establish whether hCD33+ myeloid cells are involved in tumor formation, hCD45+ cells isolated from the liver and spleen of hNSG-SGM3 mice were subdivided using magnetic beads into hCD33+ and hCD33neg cell fractions (Fig. 3 D) and used in ACT experiments as described above. Recipient mice that received hCD33+ cells showed melanoma tumors in the spleen and in the liver, while those that received hCD33neg cells did not (Fig. 3 E; with no impact on the growth of the primary tumors as shown in Fig. S2 G).
hCD11b+ cells represent a large fraction of hCD33+ cells (71% ± 14%; range, 57–87%; n = 4; Fig. 4 A), and the ACT of CD11b-depleted CD45+ cells resulted in a lower number of liver tumors in a fraction of mice (0.7 ± 0.6 in the hCD11bneg group; Fig. 4 B) while hCD11b+ cells could enhance liver tumors (12.8 ± 12.4, n = 4 mice; Fig. S2 H), suggesting that these cells play a role. hCD11b+ cells include CD66b+ cells that contain mature granulocytes and are present in hNSG-SGM3 but not in hNSG mice (Fig. S1 F), CD14+ cells of monocytic lineage, and cells with an intermediate expression of CD117 (Fig. 4 A). We did not observe any significant difference in liver tumors of mice transferred with CD66b-depleted cells or CD66b-enriched cells (Fig. S2, I and J), suggesting that CD66b+ cells are not essential for colonization of liver in hNSG-SGM3 mice. Similarly, depletion of CD14+ cells did not impact distant tumor development (Fig. S2, K and L), indicating that cells of monocytic lineage are dispensable. Thus, hCD33+ cells contain cell subset(s), distinct from mature granulocytes and monocytes, able to support melanoma growth in the liver.
Distant organ colonization is mediated by hCD33+CD11b+CD117+ cells
hCD117+ (KIT+) cells were enriched in hNSG-SGM3 mice compared with hNSG (Fig. S1 F). The expression of CD117 within hCD33+ cells was heterogeneous, with at least three cell populations detectable by surface marker expression: CD33+CD11b+CD117neg, CD33+CD11b+CD117+, and CD33+CD11bnegCD117+ (Fig. 4 A). Because NSG mice expressing membrane-bound human SCF (NSG-mSCF) develop CD117+ tryptase+ mature human mast cells (Takagi et al., 2012), we constructed hNSG-mSCF mice and implanted them s.c. with 106 Me275 cells. We did not detect tumors in the liver, and only sporadic spleen tumors in two of eight mice (Fig. 4 C), while there was a comparable primary tumor growth (Fig. S2 M). Furthermore, NSG-SGM3 mice with ACT of FCER1A-depleted hCD45+ cells displayed disseminated tumors in the liver (Fig. S2, N and O). Thus, hFCER1A+ (a marker of mature mast cells and basophils) cells are dispensable. However, depletion of hCD117+ cells resulted in a significant decrease in the number of mice with liver tumors as well as in the number of liver tumors per mouse in two independent experiments (1–35 in hCD45+ transferred mice, n = 11/13 vs. 0–6 in CD117-depleted hCD45+ transferred mice, n = 2/12; Fig. 4, D and E; and Fig. S2 P). Conversely, ACT of hCD117+ cells enriched from liver/spleen into nonhumanized NSG-SGM3 mice supported the development of liver tumors (range, 4–90) in the liver in five of five mice (Fig. 4 E and Fig. S2 P). Thus, the capacity to promote melanoma growth in distant organs lies within hCD33+CD11b+CD117+ precursor/progenitor cells, which represent ∼4% of the hCD45+ cells in hNSG-SGM3 mice.
Single-cell RNA-seq (scRNA-seq) of hCD33+ cells from the liver/spleen of hNSG-SGM3 mice (Fig. 4 F; Fig. S3, A–C; and Table S8) revealed that KIT+ cells, which coexpress ITGAM (CD11b) and IL3RA but not CSF2RA (Fig. 4 G), are composed of four clusters (Fig. 4 F, clusters 2, 3, 5, and 7; and Fig. S3, B and C), including two clusters of cells expressing transcripts coding for mast cell proteolytic enzymes (TPSAB1, TPSB2) and leukotriene catabolism (HPGD, HPGDS, LTC4S; clusters 2 and 3); one cluster of mature mast cells with high expression of high-affinity IgE receptor (FCER1A) and CCR3 (cluster 7); and one cluster of dividing progenitor cells expressing cell cycle and DNA synthesis genes (cluster 5). In line with this, tissue analysis revealed differences between CD117 and tryptase expression in both experimental metastatic tumors in hNSG-SGM3 mice and in metastasis from melanoma patients (Fig. S3, D–F). As the depletion of FCER1A-expressing cells did not impact melanoma growth in distant organs (Fig. S3 I), we conclude that pro-metastatic activity is distant from mature mast cells and is linked with progenitor cells.
We then stratified the cells into two groups based on the expression level of the KIT gene (Fig. 4 H) to establish the transcriptome of KIT+ cells. The differentially expressed genes (DEGs) between the two groups of cells were computed using the Wilcoxon rank sum test. All the genes that had an absolute log2 fold-change value >0.2 and a false discovery rate of <5% were selected as KIT signature genes (n = 221; Table S9). The prognostic significance was evaluated using the log2 fold-change weighted mean expression of the KIT signature genes in samples in TCGA (Cancer Genome Atlas Network, 2015). Since the score is a measure of the specific cell type, the samples were then stratified into two groups based on the median of the score, and the survival difference in the two groups was visualized using Kaplan-Meier plots (Fig. 4 I). The Kaplan-Meier analysis revealed that the high KIT score was associated with significantly lower survival probability (P< 0.0005; hazard ratio = 1.94; 95% confidence interval = 1.33, 2.82).
Thus, hCD33+CD11b+CD117+ myeloid cells facilitate distant organ colonization by human melanoma after subcutaneous implantation. The molecular mechanisms regulating the ability of these cells to promote tumor growth in our model remain to be identified. Importantly, despite the presence of endogenous murine myeloid cells, the distant organ colonization is sporadic in the absence of human myeloid cells. This suggests that the molecular pathways governing myeloid cell–dependent melanoma growth are restricted in the absence of human cells. Our studies herein suggest a potential novel prognostic biomarker and downstream effector molecule(s) that might represent a therapeutic target.
Materials and methods
Melanoma cancer cell line Me275 (Research Resource Identifier [RRID]:CVCL_S597), which was established from surgically excised melanoma metastases from patient LAU50, was provided by Pedro Romero at the Ludwig Institute for Cancer Research at the University of Lausanne (Lausanne, Switzerland). Tumor cells were cultured in complete RPMI (RPMI 1640, 25 mM Hepes, 1 mM sodium pyruvate, 1% nonessential amino acid, 1% penicillin-streptomycin, and 2 mM L-glutamine) supplemented with 10% FBS at 37°C with 5% CO2 atmosphere and authenticated using Short Tandem Repeat profiling analysis by the American Type Culture Collection. The mycoplasma test was performed regularly, and cells were negative for mycoplasma before each experiment.
The Me275 tumor cell lines were transduced with lentiviral vector (pLX302-CMV-Luc2) at varying multiplicity of infection by incubating virions in the culture medium containing 8 µg/ml polybrene (Sigma). Stably transduced cells were selected with 3 µg/ml puromycin (InvivoGen). Stable cell lines expressing luciferase protein were confirmed by anti-luciferase (Luci21 1–107; Novus) intracellular staining.
Humanized mice were generated on NSG (NOD.Cg-Prkdcscid Il2rgtm1Wjl/SzJ; RRID:IMSR JAX:005557), NSG-SGM3 (NOD.Cg-Prkdcscid Il2rgtm1WjlTg(CMV-IL3,CSF2,KITLG)1Eav/MloySzJ; RRID:IMSR JAX:013062), and NSG-mSCF (NOD.Cg-Prkdcscid Il2rgtm1Wjl Tg(PGK1-KITLG*220)441Daw/SzJ; RRID:IMSR JAX:017830) obtained from The Jackson Laboratory. All protocols were reviewed and approved by the Institutional Animal Care and Use Committee at The Jackson Laboratory (14005) and University of Connecticut Health Center (101163–0220). De-identified human specimens were obtained from vendors and approved by The Jackson Laboratory Institutional Review Board. Mice were sublethally irradiated (10 cGy per gram of body weight) using γ irradiation at the age of 4 wk. 100,000 CD34+ HPCs from fetal liver or full-term cord blood (Advanced Bioscience Resources or Lonza) were given by tail-vein i.v. injection in 200 µl PBS. Mice were bled at 8–12 wk after HPC transplant to evaluate engraftment and were euthanized according to the individual experimental design.
Flow cytometry analysis
For human engraftment, heparinized blood samples were first treated with RBC lysis buffer (Biolegend), followed by the treatment of both human and murine Fc Block (BD Biosciences) and then stained on ice with antibodies to mouse CD45 (30-F11; BD Biosciences) and hCD45 (HI30; BD Biosciences), CD14 (MqP9; BD Biosciences) or CD33 (P67.6; Biolegend), CD19 (HIB19; Biolegend), and CD3 (SK7; BD Biosciences) for 30 min (Table S10). Antibodies to mouse and hCD45 were species-specific antibodies to pan-leukocytes including myeloid cells. After washing twice with PBS, the samples were acquired on an LSRII or Symphony A5 (BD Biosciences) and analyzed with FlowJo software (Tree Star). For immunophenotype, bone marrow (femur and tibia), spleen, livers, lungs, and blood were collected. Tissues were first digested with 25 µg/ml Liberase (Roche Diagnostics) and DNase I (Sigma) at 37°C, 10 min for the spleen and 30 min for livers and lungs. Single-cell suspensions were made, and the debris was removed by filtering through a 70-µm cell strainer. Cells were first treated with RBC lysis buffer, followed by the treatment of both human and murine Fc Block, and then stained on ice with fluorescence-conjugated antibodies to mouse CD45 (30-F11; BD Biosciences) and hCD45 (HI30; BD Biosciences), CD3 (OKT3; BD Biosciences), CD19 (HIB19; Biolegend) or CD20 (2H7; Biolegend), CD33 (P67.6; Biolegend), CD11b (ICRF44; Biolegend), CD11c (B-ly6; BD Biosciences), CD14 (MqP9; BD Biosciences), CD16 (3G8; BD Biosciences), CD66b (G10F5; Biolegend), CD117 (104D2; Biolegend), CD127 (HIL-7R-M21; BD Biosciences), FCER1A (AER-37; Biolegend), and HLA-DR (G46-6; BD Biosciences) for 30 min (Table S10). After washing twice with PBS, the samples were stained with 7-aminoactinomycin D (Biolegend) and acquired on LSRII or Symphony A5 (BD Biosciences) and analyzed with FlowJo software (Tree Star).
Tumor cells were injected s.c. into the flank of the mice. Tumor size was monitored every 7 d with a caliper. Tumor volume (ellipsoid) was calculated as follows: (short diameter)2 × long diameter/2. Alternatively, luciferase-labeled melanoma cells were injected i.v. into the mice. Mice were killed, and the macroscopic metastases were identified and scored in various organs including lymph nodes (axillary and brachial), livers, spleen, kidneys, and lungs.
Human immune cell purification and ACT
At 12–16 wk after transplant, hNSG-SGM3 mice were euthanized, and spleen and liver were collected for single-cell suspension. Spleen and liver were first digested with 25 µg/ml Liberase (Roche Diagnostics) for 10–30 min at 37°C; single-cell suspensions were made, and the debris was removed by filtering through a 70-µm cell strainer. Live cells were isolated using Ficoll-Paque Plus density gradient centrifugation. Human immune cells were enriched by using the Mouse/Human Chimera isolation kit (StemCell Technologies) following the manufacturer’s protocol. For the enrichment of CD33+ or CD33neg cells, enriched hCD45+ cells were further stained with PE-conjugated CD33 antibody (WM53; Biolegend) for 15 min and enriched by using EasySep PE selection kit (StemCell Technologies). For CD14, CD11b, CD66b, CD117, and FCER1A depletion, hCD45+ cells were further stained with PE-conjugated CD14 (MϕP-9; BD Biosciences), CD11b (IRCF44; Biolegend), CD66b (G10F5; Biolegend), CD117 (104D2; Biolegend), and FCER1A (AER-37; Biolegend) antibodies (Table S10) for 15 min and enriched by using the EasySep PE selection kit (StemCell Technologies). Isolated human immune cells had purity exceeding 95%. Human immune cells were adoptively transferred at 107 cells per mouse by tail-vein i.v. injection.
In vivo imaging
Before mice were anesthetized with Isoflurane, an aqueous solution of luciferin (150 mg/kg i.p.) was injected 10 min before imaging with IVIS (PerkinElmer). The animals were placed into the light-tight chamber of the charge-coupled device camera system, and the photons emitted from the luciferase-expressing cells within the animal were quantified using Living Image (PerkinElmer). To image dissected organs, mice were first injected i.p. with luciferin (150 mg/kg) for 10 min and quickly killed to remove each organ. Organs were imaged in 12-well culture dishes with PBS containing 300 µg/ml luciferin.
Tissues were embedded in optimal cutting temperature media (Sakura Finetek U.S.A.) and snap-frozen in liquid nitrogen. Frozen sections were cut at 6 µm, air-dried on Superfrost plus slides, and fixed with cold acetone for 5 min. Tissue sections were first blocked with Background Buster, followed by treatment of Fc Receptor Block (Innovex Bioscience). The sections were then stained with mouse monoclonal antibodies to human MART-1 (M2-2C10 and M2-9E3; Novus Biologicals), gp100 (NK1-beteb; LifeSpan BioSciences), CD45 (HI30; Biolegend), CD33 (P67.6; Biolegend), CD11b (ICRF44), CD117 (104D2; Biolegend), and tryptase (AA1; Biolegend) for 1 h at room temperature (Table S10). Respective isotype antibodies were used as the control. Finally, sections were counterstained with 1 µg/ml of DAPI, mounted with Fluoromount (Thermo Fisher Scientific), acquired using a Leica SP 8 confocal microscope with Leica LAS X software, and analyzed using Imaris software (Bitplane).
Total RNA was isolated from snap-frozen metastatic melanoma tissues (Table S1; Cooperative Human Tissue Network, Pennsylvania) and CD33+ cells from the spleen and livers of hNSG-SGM3 and hNSG mice using the RNA isolation kit following the manufacturer’s protocol (Qiagen). Total RNA isolated was run on a Qubit (Thermo Fisher Scientific) and a Bioanalyzer 2100 Nano Chip (Agilent Technologies) to check RNA quantity and quality. Sequencing libraries were prepared using KAPA Stranded mRNA-seq kit (Roche) according to the manufacturer’s protocol. First, poly-A RNA was isolated from 300 ng total RNA using oligo-dT magnetic beads. Purified RNA was then fragmented at 85°C for 6 min, targeting fragment range 250–300 bp. Fragmented RNA was reverse transcribed with an incubation of 25°C for 10 min and 42°C for 15 min and an inactivation step at 70°C for 15 min. This was followed by second strand synthesis at 16°C for 60 min. Double-stranded cDNA fragments were purified using Ampure XP beads (Beckman Coulter), then A-tailed and ligated with Illumina adapters. Adapter-ligated DNA was purified using AMPure XP beads and followed by 10 cycles of PCR amplification. The final library was cleaned up using AMPure XP beads. Quantification of libraries was performed using real-time quantitative PCR (Thermo Fisher Scientific). Sequencing was performed on an Illumina NextSeq 500 platform generating single-end reads of 75 bp. All primary analysis of RNA-seq was processed using CASAVA pipeline (Illumina, v1.8.2). Sequences were aligned with Bowtie 2 (Kim et al., 2013), and counts were generated with RSEM (Anders et al., 2015) using the annotations from Ensembl GRCh37 (Harrow et al., 2012). The files from alignment result were converted to BAM format using SAMtools (Li et al., 2009). Raw counts were normalized to log2 transformed transcript per million (TPM) or fragments per kilobase of transcript per million mapped reads (FPKM; log2(FPKM + 1)). CIBERSORT was used to estimate the proportions of diverse immune cell types using the genes that define the signature expression of the immune cell types. We used the default 22 cell types (LM22) provided (Newman et al., 2015). For modular analysis, a set of 260 transcriptional modules was used as a preexisting framework (Banchereau et al., 2016). Module-level activity score was calculated by R package gene set variation analysis (GSVA) score from RNA-seq data (Hänzelmann et al., 2013). Ingenuity pathway analysis (IPA; Qiagen) was applied to reveal transcriptional networks, and ClueGO was used to illustrate biological interpretation of genes (Bindea et al., 2009).
Enriched hCD33+ cells from liver and spleen of hNSG-SGM3 mice were resuspended in PBS containing 0.04% BSA, the cell numbers were counted on the Contess II automated cell counter (Thermo Fisher Scientific), and ∼12,000 cells were loaded per channel on Chromium microfluidic chips (10x Genomics). Single-cell capture, barcoding, and library preparation were performed using the 10x Chromium version 2 chemistry according to the manufacturer’s protocol (10x Genomics). The quality of cDNA and libraries was checked on an Agilent 4200 TapeStation, quantified by KAPA quantitative PCR, and sequenced on a HiSeq 4000 (Illumina) to an average depth of 50,000 reads per cell. We quantified gene expression counts from raw sequencing data using Cell Ranger v2.2 with GRCh38. Datasets from liver and spleen of two independent experiments were normalized using Harmony (Korsunsky et al., 2019).
Database and statistical analysis
Statistical analysis was performed in Prism 8 (GraphPad). Figure legends denote P values as follows: ****, P < 0.0001; ***, P < 0.001; **, P < 0.01; and *, P < 0.05. Comparisons between any two groups were analyzed using the Mann-Whitney test or two-tailed t test, and comparisons between any three or more groups were analyzed by ANOVA as indicated in the respective legends. The Kaplan-Meier curves of melanoma patient data were generated using RNA-seq data from the TCGA–skin cutaneous melanoma project (Cancer Genome Atlas Network, 2015). The DEGs between the two groups of cells were computed using the Wilcoxon rank sum test. The statistical significance of the difference in the Kaplan-Meier survival plot was computed using the log-rank test using R package.
RNA-seq data have been deposited at the NCBI Sequence Read Archive with accession no. SRP141256 (https://www.ncbi.nlm.nih.gov/Traces/study1/?acc=SRP141256&go=go), and scRNA-seq data have been deposited in the NCBI Gene Expression Omnibus with accession no. GSE161957 and Sequence Read Archive with accession no. SRP293689 (https://www.ncbi.nlm.nih.gov/Traces/study1/?acc=SRP293689&go=go).
Online supplemental material
Fig. S1 shows human myeloid cells in metastatic melanoma tumors and hNSG-SGM3 mice. Fig. S2 shows that hNSG-SGM3 mice promote melanoma growth in distant organs via hCD33+ cells. Fig. S3 shows the expression of hCD117 in hNSG-SGM3 mice and metastatic melanoma tumor. Table S1 shows the list of melanoma patient tumors used in the study. Table S2 shows the list of genes in annotated immune modules. Table S3 shows the kinetics of human engraftment in the blood of hNSG and hNSG-SGM3 mice. Table S4 shows human engraftment in the tissues of hNSG and hNSG-SGM3 mice. Table S5 shows DEGs of bulk RNA-seq on hCD33+ cells enriched from the spleen and liver of hNSG and hNSG-SGM3 mice. Table S6 shows IPA on upstream regulator for the myeloid genes expressed in CD33+ cells from hNSG-SGM3 mice. Table S7 shows IPA on upstream regulator for the myeloid genes expressed in human melanoma tumors. Table S8 shows marker genes specific for each cluster in scRNA-seq of hCD33+ cells from hNSG-SGM3 mice. Table S9 shows KIT signature genes identified from scRNA-seq of hCD33+ cells from hNSG-SGM3 mice. Table S10 shows the list of antibodies used in the study.
We thank patients and healthy donors; T. Helenius, K. Oxley, S. Guha; Flow Cytometry, Microscopy, Single Cell Biology, and Genome Technologies Cores at The Jackson Laboratory for Genomic Medicine; Patient-Derived Xenograft, Research Animal Facility, and Comparative Medicine and Quality Services at The Jackson Laboratory for Mammalian Genetics; and Comparative Medicine at the University of Connecticut Health Center.
Work was supported by The Jackson Laboratory; National Institutes of Health (CA195712; P30 JAX Cancer Center grant; melanoma analysis) and Department of Defense (W81XWH-17-1-0010; hCD33+ cells analysis) to K. Palucka.
Author contributions: C.I. Yu: experiment design and performance, data analysis, and manuscript writing. J. Martinek and T.-C. Wu: tissue analysis. F. Marches: humanized mice. P. Metang, P. Authie, and V.K.P. Oliveira: experiments and tumor development. J. Martinek, K.I. Kim, J. George, E. Ahmadzadeh, V.G. Wang, and J.H. Chuang: computational analyses. P. Robson: single-cell transcriptomics. K.I. Kim: statistics. R. Maser: critical reagents. J. Banchereau: study design and manuscript writing. K. Palucka: concept, study design, data analysis, and manuscript writing.
Disclosures: C.I. Yu reported a patent to humanized mouse model for cancer metastasis pending. P. Metang reported “other” from University of Texas Southwestern Medical Center outside the submitted work. J. Banchereau reported grants from Merck during the conduct of the study; grants from Sanofi, personal fees from Cue Biopharma, personal fees from Neovacs, personal fees from Ascend Pharma, and personal fees from Georgiamune outside the submitted work; in addition, J. Banchereau had a patent to humanized mouse model for cancer metastasis pending. K. Palucka reported grants from Merck, “other” from Merck, personal fees from Cue Biopharma, and personal fees from Sobi outside the submitted work; in addition, K. Palucka had a patent on humanized mice to study metastasis pending. No other disclosures were reported.