Figure 1.
HMGA2 is expressed in HSCs, early progenitors, and erythroid lineage. (A) Overview of hematopoietic cell populations identified in human BM from the Human Cell Atlas data set (integrated data from 8 donors, Uniform Manifold Approximation and Projection [UMAP] reduction, preprocessed data, clusters, and labels adopted from Hay et al22). CD34+ HSC cluster is indicated by the black arrow. (B) UMAP plot of HMGA2, CD34, and PCNA expression (MAGIC imputation). (C) Single-cell transcriptomic overview of hematopoietic cell populations identified in human CB cells. Fresh and UM171-expanded CD34+ cells (7 days) were integrated and clustered using Seurat 3 (2 samples each condition, 15 921 cells total). Fifteen cell clusters (left) were identified and defined using Seurat (v3) procedure: HSCs, multipotent progenitors (MPP), lymphoid-primed multipotent progenitors (LMPP), granulo-monocytic progenitors (GMP), megakaryocyte-erythroid progenitors (MEP), common lymphoid progenitors (CLP), pre-dendritic cells (pre-DC), plasmacytoid dendritic cells (pDC), myeloid dendritic cells (mDC), monocytes (Mono), neutrophils (Neut), erythroid progenitors (ERP), megakaryocytes (MK), erythrocytes (Ery), and eosinophils/basophils/mast cells(Eo/Bas/Ma). Unsupervised ordering of the HSCs was done with Seurat 3 integrated results as input to build a tree-like differentiation trajectory using the DDRTree algorithm of the Monocle v3 R package (right). (D) UMAP plot of representative stem cell and lineage associated genes compared with HMGA2 expression (integrated data from fresh and UM171-expanded CB cells, MAGIC imputation). (E) UMAP plot of representative stem cell, lineage, and proliferative genes in fresh CD34+ CB cells vs UM171 ex vivo expanded cells (MAGIC imputation). Red circle: non-proliferative CD34+ cells, orange circle: proliferative CD34+ FLT3+ progenitors. (F) Irradiated NSG mice were transplanted with CD34+ cells infected with short hairpin (sh) RNA green fluorescent protein (GFP) vectors targeting HMGA2 gene or a control locus. Twenty weeks after transplantation, reconstitution was assessed by measuring the percentage of human CD45+ GFP+ cells in BM (n = 6, median is depicted, Mann-Whitney U test). Gran, granulocytes.

HMGA2 is expressed in HSCs, early progenitors, and erythroid lineage. (A) Overview of hematopoietic cell populations identified in human BM from the Human Cell Atlas data set (integrated data from 8 donors, Uniform Manifold Approximation and Projection [UMAP] reduction, preprocessed data, clusters, and labels adopted from Hay et al22 ). CD34+ HSC cluster is indicated by the black arrow. (B) UMAP plot of HMGA2, CD34, and PCNA expression (MAGIC imputation). (C) Single-cell transcriptomic overview of hematopoietic cell populations identified in human CB cells. Fresh and UM171-expanded CD34+ cells (7 days) were integrated and clustered using Seurat 3 (2 samples each condition, 15 921 cells total). Fifteen cell clusters (left) were identified and defined using Seurat (v3) procedure: HSCs, multipotent progenitors (MPP), lymphoid-primed multipotent progenitors (LMPP), granulo-monocytic progenitors (GMP), megakaryocyte-erythroid progenitors (MEP), common lymphoid progenitors (CLP), pre-dendritic cells (pre-DC), plasmacytoid dendritic cells (pDC), myeloid dendritic cells (mDC), monocytes (Mono), neutrophils (Neut), erythroid progenitors (ERP), megakaryocytes (MK), erythrocytes (Ery), and eosinophils/basophils/mast cells(Eo/Bas/Ma). Unsupervised ordering of the HSCs was done with Seurat 3 integrated results as input to build a tree-like differentiation trajectory using the DDRTree algorithm of the Monocle v3 R package (right). (D) UMAP plot of representative stem cell and lineage associated genes compared with HMGA2 expression (integrated data from fresh and UM171-expanded CB cells, MAGIC imputation). (E) UMAP plot of representative stem cell, lineage, and proliferative genes in fresh CD34+ CB cells vs UM171 ex vivo expanded cells (MAGIC imputation). Red circle: non-proliferative CD34+ cells, orange circle: proliferative CD34+ FLT3+ progenitors. (F) Irradiated NSG mice were transplanted with CD34+ cells infected with short hairpin (sh) RNA green fluorescent protein (GFP) vectors targeting HMGA2 gene or a control locus. Twenty weeks after transplantation, reconstitution was assessed by measuring the percentage of human CD45+ GFP+ cells in BM (n = 6, median is depicted, Mann-Whitney U test). Gran, granulocytes.

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