Presentation is loading. Please wait.

Presentation is loading. Please wait.

Fig. 7. SCF and IGF-1 accelerate fetal spleen erythropoiesis in vivo.

Published byGözde Uzunlar Modified over 5 years ago

Similar presentations

Presentation on theme: "Fig. 7. SCF and IGF-1 accelerate fetal spleen erythropoiesis in vivo."— Presentation transcript:

1 Fig. 7. SCF and IGF-1 accelerate fetal spleen erythropoiesis in vivo.
SCF and IGF-1 accelerate fetal spleen erythropoiesis in vivo. (A) Gating strategy of flow cytometric analysis. CD45−c-Kit−CD71+/−Ter119+ defines terminally-differentiating erythroid cells and mature red blood cells. (B) Graph showing the number of terminally-differentiating erythroid cells and mature red blood cells in mice treated with DMSO, the SCF inhibitor, the IGF-1R inhibitor or both, two hours after injection (n = 3). (C) Relative expression (RQ) of erythroid genes such as Gata1, Klf1 and β-major globin mRNAs in CD45− cells was examined by real-time PCR. CD45− cells from mice injected with DMSO served as controls (n = 3). Data are means±standard deviation (SD). *P<0.05. Keai Sinn Tan et al. Biology Open 2015;bio © Published by The Company of Biologists Ltd

Download ppt "Fig. 7. SCF and IGF-1 accelerate fetal spleen erythropoiesis in vivo."

Similar presentations

Quantitative analysis of murine terminal erythroid differentiation in vivo: novel method to study normal and disordered erythropoiesis by Jing Liu, Jianhua.

Quantitative analysis of murine terminal erythroid differentiation in vivo: novel method to study normal and disordered erythropoiesis by Jing Liu, Jianhua.
by Jessica M. Salmon, Nicholas J. Slater, Mark A. Hall, Matthew P

by Jessica M. Salmon, Nicholas J. Slater, Mark A. Hall, Matthew P
Differentiation of AZD4785 from MAPK pathway inhibitors in vitro

Differentiation of AZD4785 from MAPK pathway inhibitors in vitro
Developmental- and differentiation-specific patterns of human γ- and β-globin promoter DNA methylation by Rodwell Mabaera, Christine A. Richardson, Kristin.

Developmental- and differentiation-specific patterns of human γ- and β-globin promoter DNA methylation by Rodwell Mabaera, Christine A. Richardson, Kristin.
Cooperative signaling between cytokine receptors and the glucocorticoid receptor in the expansion of erythroid progenitors: molecular analysis by expression.

Cooperative signaling between cytokine receptors and the glucocorticoid receptor in the expansion of erythroid progenitors: molecular analysis by expression.
Identification and characterization of 2 types of erythroid progenitors that express GATA-1 at distinct levels by Norio Suzuki, Naruyoshi Suwabe, Osamu.

Identification and characterization of 2 types of erythroid progenitors that express GATA-1 at distinct levels by Norio Suzuki, Naruyoshi Suwabe, Osamu.
The exosome complex establishes a barricade to erythroid maturation

The exosome complex establishes a barricade to erythroid maturation
MEK kinase 1 activity is required for definitive erythropoiesis in the mouse fetal liver by Barbara Bonnesen, Cathrine Orskov, Susanne Rasmussen, Peter.

MEK kinase 1 activity is required for definitive erythropoiesis in the mouse fetal liver by Barbara Bonnesen, Cathrine Orskov, Susanne Rasmussen, Peter.
Leukemia involves the accumulation of ISP CD8+T-cells and blockages in B-cell development. Leukemia involves the accumulation of ISP CD8+T-cells and blockages.

Leukemia involves the accumulation of ISP CD8+T-cells and blockages in B-cell development. Leukemia involves the accumulation of ISP CD8+T-cells and blockages.
Twist1 regulates embryonic hematopoietic differentiation through binding to Myb and Gata2 promoter regions by Kasem Kulkeaw, Tomoko Inoue, Tadafumi Iino,

Twist1 regulates embryonic hematopoietic differentiation through binding to Myb and Gata2 promoter regions by Kasem Kulkeaw, Tomoko Inoue, Tadafumi Iino,
Fig. 1. Heme and globin during normal erythropoiesis, hypothesis, and DBA patient 1’s marrow aspirate. Heme and globin during normal erythropoiesis, hypothesis,

Fig. 1. Heme and globin during normal erythropoiesis, hypothesis, and DBA patient 1’s marrow aspirate. Heme and globin during normal erythropoiesis, hypothesis,
Fig. 2. Effect of endurance training on gene expression, and protein content and activity in heart muscle. Effect of endurance training on gene expression,

Fig. 2. Effect of endurance training on gene expression, and protein content and activity in heart muscle. Effect of endurance training on gene expression,
Fig. 5. Prip silencing enhances the co-localization of GABARAP with insulin vesicles and β-tubulin.Co-localization of GABARAP (green) with insulin (red)

Fig. 5. Prip silencing enhances the co-localization of GABARAP with insulin vesicles and β-tubulin.Co-localization of GABARAP (green) with insulin (red)
Fig. 2. Outline of the two types of stimulus sequences employed in the analysis.(A) Environment information stimuli; (B) adaptation stimuli. Outline of.

Fig. 2. Outline of the two types of stimulus sequences employed in the analysis.(A) Environment information stimuli; (B) adaptation stimuli. Outline of.
Fig. 5. Effect of gravity and stage on relative expression levels of molecular core clock and clock regulatory genes.Total RNA was isolated from (A) mammary.

Fig. 5. Effect of gravity and stage on relative expression levels of molecular core clock and clock regulatory genes.Total RNA was isolated from (A) mammary.
Representative flow cytometric analysis of bone marrow, spleen and whole blood from EpoWT/WT, EpoΔ/Δ and EpoWT/Δ mice. Representative flow cytometric analysis.

Representative flow cytometric analysis of bone marrow, spleen and whole blood from EpoWT/WT, EpoΔ/Δ and EpoWT/Δ mice. Representative flow cytometric analysis.
Fig. 7. Motion adaptation increases time-dependent response modulations (TDRM) relatively to the average cell response.TDRM normalized to the value obtained.

Fig. 7. Motion adaptation increases time-dependent response modulations (TDRM) relatively to the average cell response.TDRM normalized to the value obtained.
Fig. 1. Muscle-specific PITX1 over-expression in the Pitx1 transgenic mice.(A) Detection of Pitx1 mRNA expression in muscles of the Pitx1 transgenic mice.

Fig. 1. Muscle-specific PITX1 over-expression in the Pitx1 transgenic mice.(A) Detection of Pitx1 mRNA expression in muscles of the Pitx1 transgenic mice.
Fig. 2. abu/pqn genes are expressed in the pharyngeal cuticle

Fig. 2. abu/pqn genes are expressed in the pharyngeal cuticle
Fig. 4. A primary screen based on scrape closure

Fig. 4. A primary screen based on scrape closure

Similar presentations

Ads by Google