The Role of Rac Signaling in The Perivascular Niche

Similar documents
Perivascular deletion of murine Rac reverses the ratio of marrow arterioles and sinusoid vessels and alters hematopoiesis in vivo

Chronic variable stress activates hematopoietic stem cells

Meeting Report. From December 8 to 11, 2012 at Atlanta, GA, U.S.A

Supplementary Figure 1. Successful excision of genes from WBM lysates and

SUPPLEMENTARY INFORMATION

SUPPLEMENTARY INFORMATION

Hematopoiesis. - Process of generation of mature blood cells. - Daily turnover of blood cells (70 kg human)

X P. Supplementary Figure 1. Nature Medicine: doi: /nm Nilotinib LSK LT-HSC. Cytoplasm. Cytoplasm. Nucleus. Nucleus

DISCLOSURE. I have the following financial relationships:

Deficiency of Lipid Phosphatase SHIP Enables Long-Term Reconstitution of Hematopoietic InductiveBoneMarrowMicroenvironment

SUPPLEMENTARY INFORMATION

Nature Immunology: doi: /ni Supplementary Figure 1. Huwe1 has high expression in HSCs and is necessary for quiescence.

Nature Immunology: doi: /ni Supplementary Figure 1. Cellularity of leukocytes and their progenitors in naive wild-type and Spp1 / mice.

The nucleotide sugar UDP-glucose mobilizes long-term repopulating primitive hematopoietic cells

Dickkopf-1 promotes hematopoietic regeneration via direct and niche-mediated mechanisms

THE HYPOXIC HEMATOPOIETIC STEM CELL NICHE Consequences of Hypoxiainduced Transcription on Stem Cell Fate

Bone Marrow Stroma in Myelodysplastic Syndromes

SUPPLEMENTARY INFORMATION

SUPPLEMENTARY INFORMATION doi: /nature12026

Selective Enhancement of Donor Hematopoietic Cell Engraftment by the CXCR4 Antagonist AMD3100 in a Mouse Transplantation Model

CD34+ Cells: A Comparison of Stem and Progenitor Cells in Cord Blood, Peripheral Blood, and the Bone Marrow

sequences of a styx mutant reveals a T to A transversion in the donor splice site of intron 5

Stem Cell Reports Ar ticle

Highly Efficient CRISPR/Cas9 Gene Editing and Long-Term Engraftment of Human Hematopoietic Stem and Progenitor Cells

Current Developments in Mobilization of Hematopoietic Stem and Progenitor Cells and Their Interaction with Niches in Bone Marrow

Haematopoietic stem cell (HSC) niches are present in diverse tissues

TISSUE-SPECIFIC STEM CELLS

Accelerate Your Research with Conversant Bio

Dynamic niches in the origination and differentiation of haematopoietic stem cells

Nature Immunology: doi: /ni.3412

Leukaemogenic effects of Ptpn11 activating mutations in the stem cell microenvironment

BCR-ABL - LSK BCR-ABL + LKS - (%)

Haematopoietic stem cells

Supplementary Information. Tissue-wide immunity against Leishmania. through collective production of nitric oxide

Stem cells: units of development and regeneration. Fernando D. Camargo Ph.D. Whitehead Fellow Whitehead Institute for Biomedical Research.

high percentage of treated patients, and may also stimulate other lineages (2-9). In rodents,

Induction of myocardial regeneration to attenuate cardiotoxicity

HSC Niche Biology and HSC Expansion Ex Vivo

Protein Tyrosine Phosphatase Receptor Type S (PTPRS) Regulates Hematopoietic Stem. Cell Self-Renewal. Mamle Quarmyne

TISSUE-SPECIFIC STEM CELLS

IN VIVO IMAGING OF THE HEMATOPOIETIC STEM CELL ENGRAFTMENT PROCESS IN THE MOUSE TIBIA BONE

Hematopoietic Stem Cell Niches Produce Lineage- Instructive Signals to Control Multipotent Progenitor Differentiation

Molecular Characterization of Leukemia Stem Cell Development. Scott A. Armstrong MD, Ph.D.

Erythropoietin preserves the endothelial differentiation potential of cardiac progenitor cells and attenuates heart failure during anti-cancer therapy

TISSUE-SPECIFIC STEM CELLS

activation with anti-cd3/cd28 beads and 3d following transduction. Supplemental Figure 2 shows

SUPPLEMENTARY FIGURES

Effective Targeting of Quiescent Chronic Myelogenous

Iliac Crest: The Gold Standard

Figure S1. Generation of inducible PTEN deficient mice and the BMMCs (A) B6.129 Pten loxp/loxp mice were mated with B6.

Supplement Material. Spleen weight (mg) LN cells (X106) Acat1-/- Acat1-/- Mouse weight (g)

Supplementary Figure 1. Characterization of basophils after reconstitution of SCID mice

TISSUE-SPECIFIC STEM CELLS

New Frontiers in Atherosclerotic Disease and Myocardial Infarction: From local inflammation to systemic stem and progenitor cell reaction

Tbk1-TKO! DN cells (%)! 15! 10!

Suppression of Cytochrome P450 Reductase Enhances Long-Term Hematopoietic Stem Cell Repopulation Efficiency in Mice

VEGFR2-Mediated Vascular Dilation as a Mechanism of VEGF-Induced Anemia and Bone Marrow Cell Mobilization

and follicular helper T cells is Egr2-dependent. (a) Diagrammatic representation of the

Identification of a Stroma-Mediated Wnt/b-Catenin Signal Promoting Self-Renewal of Hematopoietic Stem Cells in the Stem Cell Niche

Quantitative PPARγ expression affects the balance between tolerance and immunity

SUPPLEMENTARY INFORMATION

BL-8040: BEST-IN-CLASS CXCR4 ANTAGONIST FOR TREATMENT OF ONCOLOGICAL MALIGNANCIES. Overview and Mechanism of Action Dr.

Stem cells are undifferentiated cells which are maintained within a specific niche. A stem cell

Supplemental Figure 1. Signature gene expression in in vitro differentiated Th0, Th1, Th2, Th17 and Treg cells. (A) Naïve CD4 + T cells were cultured

February 14, 2003 Report on preclinical studies in gc-ko mice Fabio Candotti

UMBILICAL CORD BLOOD STEM CELLS EXPANDED IN THE PRESENCE OF NICOTINAMIDE (NICORD) PROVIDE LONG TERM MULITI-LINEAGE ENGRAFTMENT

Supplementary Figure 1. Efficient DC depletion in CD11c.DOG transgenic mice

Supplementary Figure S1. PTPN2 levels are not altered in proliferating CD8+ T cells. Lymph node (LN) CD8+ T cells from C57BL/6 mice were stained with

Supplementary Figure 1: Expression of NFAT proteins in Nfat2-deleted B cells (a+b) Protein expression of NFAT2 (a) and NFAT1 (b) in isolated splenic

Supplementary Figures

Journal Club WS 2012/13 Stefanie Nickl

% of live splenocytes. STAT5 deletion. (open shapes) % ROSA + % floxed

Getting to the root of Cancer

SUPPLEMENTARY FIGURES

SUPPLEMENTARY INFORMATION

Endogenous TNFα orchestrates the trafficking of neutrophils into and within lymphatic vessels during acute inflammation

SUPPLEMENTARY INFORMATION

CRISPR-mediated Editing of Hematopoietic Stem Cells for the Treatment of β-hemoglobinopathies

Normal and Leukemic Stem Cell Niches: Insights and Therapeutic Opportunities

Humanized models to study myeloid malignancies. Prof. Dominique Bonnet Hematopoietic Stem Cell Lab Francis Crick Institute, London, UK

Stem cells and Cancer. John Glod. December 2, 2009

Canberra, Australia). CD11c-DTR-OVA-GFP (B6.CD11c-OVA), B6.luc + and. Cancer Research Center, Germany). B6 or BALB/c.FoxP3-DTR-GFP mice were

Hematopoiesis/Hematopoiesis Physiology

Spleens of myelofibrosis patients contain malignant hematopoietic stem cells

BONE MERROW MESENCHYMAL STEM AND PROGENITOR CELLS IN MYELOID MALIGNANCIES

Eosinophils are required. for the maintenance of plasma cells in the bone marrow

Placental Growth Factor Expression Is Required for Bone Marrow Endothelial Cell Support of Primitive Murine Hematopoietic Cells

Ischemic Stroke Activates Hematopoietic Bone Marrow Stem Cells

Lymphoid architecture & Leukocyte recirculation. Thursday Jan 26th, 2017

TISSUE-SPECIFIC STEM CELLS

Supplemental Figure 1. Activated splenocytes upregulate Serpina3g and Serpina3f expression.

NIH Public Access Author Manuscript Leukemia. Author manuscript; available in PMC 2013 May 01.

Supplementary Information. Paired immunoglobulin-like receptor A is an intrinsic, self-limiting

BCR-ABL uncouples canonical JAK2-STAT5 signaling in chronic myeloid

pro-b large pre-b small pre-b CCCP (µm) Rag1 -/- ;33.C9HCki

TISSUE-SPECIFIC STEM CELLS

Functional ramifications for the loss of P-selectin expression on hematopoietic and leukemic stem cells

Mariusz Z. Ratajczak M.D., Ph.D., d.hc. Stem Cell Institute at the James Graham Brown Cancer Center, University of Louisville.

Schumacher et al. Journal of Hematology & Oncology (2015) 8:64 DOI /s

ECM1 controls T H 2 cell egress from lymph nodes through re-expression of S1P 1

Transcription:

The Role of Rac Signaling in The Perivascular Niche Felicia Ciuculescu Diaspora and Higher Education and Research Perspectives in Personalized Medicine- from Concept to Clinical Application Center for Gene and Cell Therapies of Cancer, Timisoara, Romania 26.4.16

Bone Marrow Stem Cell Niche Mesenchymal Stromal Cells: Nestin + MSCs:.8% of BM nucleated cells Immunopheno type: CD45 - CD31 - Ter119 - PDGFRα + CD51 + Murine: Lepr-Cre Cxcl12-GFP Nes-GFP, etc. Human: CD146 Immunopheno type: CXCL12 SCF Angp-1 VCAM-1 Nestin + cells required for HSCs/ progenitors homing Modified according to Morrison & Scadden. 214

Rac GTPases and their function in nonhematopoietic cells Rac GTPases: members of the Rho GTPase family and act as molecular switches integrating environmental signals. Mammalian Rac GTPases: Rac1, Rac2, Rac3 Rac1 is ubiquitously expressed Rac2 is expressed in hematopoietic cells Rac3 is widely expressed but mainly in CNS In vitro Inhibition of Rac1 promotes BMP2-induced osteoblastic differentiation (Oniashi et al. 213) Critical for OB adhesion, spreading, and proliferation (Jung et al. 211) Critical for MSCs differentiation into chondrocytes (Sosa-García et al. 21) Impaired OB migration (Fukuyama et al. 24) Rac1 function in osteoblasts (OB) WT In vivo OB-Rac del Trabecular microct Rac deletion from osteoblastic niche leads to reduced trabecular bone formation but normal hematopoiesis Lane et al. 211

Hypothesis The deletion of Rac in Nestin + cells will disrupt the perivascular hematopoietic niche and HSC function and hematopoiesis

Rac deletion in perivascular space affects: Vascular architecture Medullary bone formation Hematopoiesis

Isolation of Nestin + cells and confirmation of Rac1 excision in perivascular niche TG Rac1 / Rac3 -/- harvest BM isolate CD45- (MACS) stain CD45 CD31 Ter119 PDGFRα CD51 Rac1 fl/fl Rac1 / Rac1 wt TG WT 1 Nestin + cells 2 TG Rac1 / Rac3 -/- Rac1 fl/fl 3 4 water (-ve) 3 2 1 PDGFRα + Nestin + cells CD51 + Nestin-Cre expression leads to partial deletion of Rac in vivo in perivascular bone marrow cells 7AAD + sort CD45 + CD31 + Ter119 +

Rac1 and Rac3 deficiency in perivascular niche leads to reduced number of Nestin + cells Nestin + cells in BM % of Nestin + cells (of BM).1.5. ** mean+/-sd, n=3,**p<.1

Rac1 and Rac3 excision in perivascular niche leads to reduced proliferative capacity and enhanced apoptosis of Nestin + cells PDGFRα+ Nestin + cells CD51+ # of cells (x1 4 ) % of appoptotic cells 2 TG WT TG Rac1 / Rac3 -/- 1 * day day 8 day 16 mean+/-sd, n=4,*p<.5 Annexin V 4 *** 2 mean+/-sd, n=3,***p<.1 *

Rac1 and Rac3 excision from perivascular niche leads to decrease number of Nestin + cells Nestin + cells participate in direct migration of HSC/progenitors (Mendez-Ferrer et al. 21)

Deficiency of Rac1 and Rac3 in the perivascular space is associated with reduced homing of LDBMs Methods C57BL6 mice DiD + homing effiency (%).2 isolate.1. LDBM stain Vybrant DiD Dye *** inject 2x1 6 LDBM cells/mouse 11.3 Gy 12hrs harvest Homed cells FACS Vybrant DiD BM Dye + cells TG WT TG Rac1 / Rac3 -/- mean+/-sd, n=15,***p<.1 Deletion of Rac genes in Nestin + cells in vivo impairs homing of HSC/progenitors to BM

Deficiency of Rac1 and Rac3 in the perivascular space leads to increase in sinusoidal and decrease in arteriolar distribution Laminin Endoglin Sca-1 Merged TG Rac1 / Rac3 -/- TG WT Laminin- arteries & sinusoids Sca-1- arteries Endoglin- sinusoids Shin-Young Park Kimberly Canty

Deficiency of Rac1 and Rac3 in the perivascular space leads to increased in sinusoidal volume and decreased in arteriolar volume % change in sinusoidal volume 2 * 1 % change in arteriolar volume 15 * 75 mean+/- SEM, n=4, p<.5 mean+/- SEM, n=4, p<.5

Rac1 and Rac3 deficiency in perivascular niche leads to increased and enlarged sinusoids PM Endoglin Laminin DAPI TG WT DIA DM 5µm 2µm 2µm PM Endoglin Laminin DAPI Frequency (%) 1 5 * ** ** TG Rac1 / Rac3 -/- DIA DM 5µm 2µm 2µm <1 µm 1-2 µm >2 µm sinusoid diameters (µm) mean+/-sem, n=3, *p<.5, **p<.1 Shin-Young Park Kimberly Canty

Rac1 and Rac3 deficiency in perivascular niche leads to increased vascular sinusoidal niche area contoured endoglin signal Endoglin DAPI TG WT TG Rac1 / Rac3 -/- 5µm 5µm 2µm 2µm 2µm 2µm 2µm 2µm % change in sinusoidal area 2 * 1 mean+/-sem, n=3, *p<.5 Shin-Young Park Kimberly Canty

Rac1 and Rac3 deficiency in perivascular niche leads to decrease in vascular arteriolar niche area TG WT TG Rac1 Rac3 -/- % change in arteriolar area 2 * 1 mean± SEM, n=3, *p<.5 Sca-1- arteries Shin-Young Park Kimberly Canty

Rac1 and Rac3 deficiency in perivascular space leads to increased trabecular bone formation femur TG WT coronal # of trabecule/ femur transverse sagittal 2 ** 1 TG Rac 1 / Rac3-/- % of trabecular bone volume TG WT TG Rac1 / Rac3-/- *** 6 3 TG WT TG Rac1 / Rac3-/-

Rac1 and Rac 3 deletion in Nestin + cells leads to increased in osteoblast progenitor cells 3 ** % of cells 15 * ALCAM + - - Sca-1 - + + ALCAM+ Osteopontin (% relative to GAPDH) mean+/-sd, n=3,*p<.5, **p<.1 Sca-1+ The deletion of Rac1 and Rac3 in Nestin + cells upregulates osteopontin expression and increases osteoblast progenitors 3 15 **

Deficiency of Rac1 and Rac3 in the perivascular space is associated with decreased HSC and progenitor cell populations 2 Stem cells * BM Progenitors LSK (x1 4 ) LT-HSC (x1 3 ) 1 1 5 ** BM- CFU/ 2.5x1 3 cells 2 ** 1 mean+/-sem, n=6,*p<.5, **p<.1 mean+/-sem, n=8,**p<.1, ***p<.1

Rac deletion in Nestin + cells decreases HSC and affects progenitors competitive repopulation capacity Competitors Rac del (TG Rac1 / Rac3 -/- ) CD45.1 CD45.1/2 CD45.2 Lethally irradiated recipients Donor derived cells in PB (%) 1 5 * * * wks 4 wks 8 wks 12 wks Competitor WT (CD45.1) TG Rac1 / Rac3 -/- (CD45.2) CD45.1 mean+/-sd, n=4, p<.1 CD45.2 Deletion of Rac genes in Nestin + cells impairs the donor-derived reconstitution capacity of HSPC

Deficiency of Rac1 and Rac3 in the perivascular space is associated with increased HSC and progenitor cell populations in spleen 1 ns 1 * LSK (x1 3 ) 5 LT-HSC (x1 3 ) 5 mean+/-sem, n=6,*p<.5, ns- not significant

Bone marrow perivascular stromal cells regulate HSCs maintenance in the hematopoietic microenvironment Nestin + cells, CAR cells and LepR + cells: perivascular stromal cells largely overlap (Mendelson and Frenette, 214) LepR + cells: main source of HSCs maintenance regulators, Scf and Cxcl12 (Zhou et al. 214) LepR + cells overlap with Nestin + GFP cells, contribute to bone and adipocyte regeneration (Mizoguchi et al. 214, Zhou et al. 214)

Rac1 and Rac3 excision in Nestin + cells leads to decrease in expression of HSC maintenance regulators, Scf and CXCL12 Normalized Scf mrna (%) Normalized m22 Scf mrna (%) 15 * 75 15 75 * Normalized Cxcl12 mrna (%) 15 75 * mean+/-sem, n=3,*p<.5

Conclusions Deficiency of Rac1 and Rac3 in the perivascular space is associated with: Decrease in Nestin + cells Decreased homing of WT hematopoietic cells into the medullary space Aberrant microvascular organization and medullary trabecular bone formation with reduced expression of factors supporting HSC Decrease in HSC and progenitor cell populations and their competitive repopulation capacity

Implication of the data Rac signaling is important for the interaction between HM constituents and HSCs and confirms the complexity of the HM with respect to the contribution of different cell types to the HSCs niche

Future aims to address experimental approaches Signaling pathways: AKT, JNK, STAT5, MAPK/PI3K Engraftment studies Nestin + cells: multi-potent capacity SNC interaction with hematopoietic microenvironment

Acknowledgments Williams Lab Prof Dr. David A Williams Serena DeVita Swaroopa Guda Pavan Nagaruri Gonchi Christian Brendel Meaghan McGuinness Chad Harris Silbestein Lab FACS Core Facility Scadden Lab Shin-Young Park Kimberly Canty Mahnaz Paktinat Ronald Mathieu David Scadden Vionne Yu Ebert s Lab Rebekka Schneider- Kramann