The ontogeny of hematopoiesis in zebrafish.

Slides:



Advertisements
Similar presentations
Microglia are tissue-resident macrophages in the CNS.
Advertisements

Chapter 16 Essential Concepts in Molecular Pathology Companion site for Molecular Pathology Author: William B. Coleman and Gregory J. Tsongalis.
Adult Stem Cells Stem Cells, Bone Marrow and Blood
Lineages and Stem Cells: B-cell development. The Circulatory System The circulatory system consists of the heart (to pump blood),the blood vessels (to.
Lecture 1 Hematopoiesis, Abdulkarim Aldosari
DEVELOPMENT OF THE CIRCULATORY SYSTEM
MESODERMAL DERIVATIVES By: Dr. Mujahid Khan. Derivatives  Connective tissue  Cartilage  Bone  Striated & smooth muscles  Heart  Blood & lymphatic.
Haematopoiesis Dr. Khadija  PHASES OF HAEMOPOIESIS  SITES OF HAEMOPOIESIS  BONE MARROW.
Circulatory System Gilbert: Chapter 14, 17. Fetal vs. Newborn Circulation (mammals) Must be specialized depending on whether oxygen comes from placenta.
Manifestation of Novel Social Challenges of the European Union in the Teaching Material of Medical Biotechnology Master’s Programmes at the University.
5. DEVELOPMENT OF BLOOD.
MLAB Hematology Keri Brophy-Martinez
MLAB Hematology Keri Brophy-Martinez Chapter 4 : Hematopoietic Organs.
Cell Differentiation and Regeneration The number of cells from any organism ranges from one to trillions. However, even the most complex organisms have.
The stroke size should be 0.25
Kuby Immunology, 7e: Chapter 2
MLAB Hematology Keri Brophy-Martinez
Hiroo Ueno, Irving L. Weissman  Developmental Cell 
Erythropoiesis Sunita Mittal.
anatomy of the immune system
Pluripotent stem cell based gene therapy for hematological diseases
Al-Mustansiriya University Collage of Pharmacy
HEMATOPOESIS Semmelweis University, Faculty of Medicine
Red bone marrow, erythropoiesis. Formation of leukocytes
Zebrafish homolog of the leukemia gene CBFB: its expression during embryogenesis and its relationship to scland gata-1 in hematopoiesis by Trevor Blake,
A blood flow–dependent klf2a-NO signaling cascade is required for stabilization of hematopoietic stem cell programming in zebrafish embryos by Lu Wang,
Fate Mapping Embryonic Blood in Zebrafish: Multi- and Unipotential Lineages Are Segregated at Gastrulation  Rachel M. Warga, Donald A. Kane, Robert K.
Blood Development: Hematopoietic Stem Cell Dependence and Independence
The embryonic origins of erythropoiesis in mammals
Volume 11, Issue 12, Pages (June 2015)
Hematopoiesis: An Evolving Paradigm for Stem Cell Biology
by Raman Sood, Milton A. English, Christiane L
James B Turpen, Clair M Kelley, Paul E Mead, Leonard I Zon  Immunity 
Cells and organs of Immune system
by Alex Bukrinsky, Kevin J. P
Macrophage-specific gene functions in Spi1-directed innate immunity
Definitive Hematopoiesis Is Autonomously Initiated by the AGM Region
Transcriptional Control of Endothelial Cell Development
Stem-cell trafficking at vascular borders
Hematopoietic stem cell
Martin Gering, Roger Patient  Developmental Cell 
Hiroo Ueno, Irving L. Weissman  Developmental Cell 
Hematopoiesis from embryonic stem cells: lessons from and for ontogeny
Il1b is required for the early and late recruitment of neutrophils but not macrophages. Il1b is required for the early and late recruitment of neutrophils.
Katrin Ottersbach, Elaine Dzierzak  Developmental Cell 
The Placenta Is a Niche for Hematopoietic Stem Cells
Yolk-sac hematopoiesis
Volume 2, Issue 3, Pages (March 2008)
Derek Cain, Motonari Kondo, Huaiyong Chen, Garnett Kelsoe 
Embryonic origins of mammalian hematopoiesis
Arterial identity of hemogenic endothelium: a key to unlock definitive hematopoietic commitment in human pluripotent stem cell cultures  Igor I. Slukvin,
Engineering Hematopoietic Stem Cells: Lessons from Development
A Crucial Interaction between Embryonic Red Blood Cell Progenitors and Paraxial Mesoderm Revealed in spadetail Embryos  Laurel A. Rohde, Andrew C. Oates,
Blood Development: Hematopoietic Stem Cell Dependence and Independence
SCL: From the origin of hematopoiesis to stem cells and leukemia
Volume 17, Issue 9, Pages (November 2016)
Tissue-Resident Macrophage Ontogeny and Homeostasis
Stem Cell Trafficking in Tissue Development, Growth, and Disease
Kiran Batta, Magdalena Florkowska, Valerie Kouskoff, Georges Lacaud 
Microglia: Multitasking Specialists of the Brain
Gfi1aa/1b do not mediate Npas4l/Cloche suppression in primitive red blood cells. Gfi1aa/1b do not mediate Npas4l/Cloche suppression in primitive red blood.
B-1 B Cell Development in the Fetus and Adult
Gfi1aa suppresses the endothelial gene expression program in primitive erythroblasts developing from the posterior lateral mesoderm. Gfi1aa suppresses.
Fig. 4. Abdominal aortic aneurysm formation in zebrafish embryos following treatment with Angiotensin II or snuff extract. Abdominal aortic aneurysm formation.
Volume 8, Issue 6, Pages (June 2017)
Comparison ofMyc-induced zebrafish liver tumors with different stages of human HCC and seven mouse HCC models. Comparison ofMyc-induced zebrafish liver.
Volume 27, Issue 5, Pages e5 (April 2019)
Model of the Ang-1 pathway in early lung development.
Fig. 2. Tbx1 lineage is largely complementary to the NSD
Shifts in site of hematopoiesis during mouse and human development.
Presentation transcript:

The ontogeny of hematopoiesis in zebrafish. The ontogeny of hematopoiesis in zebrafish. (A) Hematopoiesis in zebrafish occurs in consecutive waves. Embryonic primitive hematopoiesis (yellow) starts at around 11 hours post fertilization (hpf) when hemangioblasts (which have the potential to become either endothelial vascular cells or hematopoietic cells, shown in white) appear in the anterior lateral mesoderm (ALM) and posterior lateral mesoderm (PLM), which collectively are analogous to the blood islands in the mammalian yolk sac. Hemangioblasts in the PLM later converge medially to form the intermediate cell mass (ICM; not shown), where primitive erythrocytes (red) predominantly arise. The ALM, which later becomes the rostral blood island (RBI; not shown), is the major site for primitive myeloid cells (blue). At around 24 hpf, embryonic erythrocytes enter circulation. As circulation begins, hematopoiesis within the ICM gradually diminishes. A transient definitive wave (pink) initiates shortly after multi-lineage erythromyeloid progenitors appear in the posterior blood island (PBI). Starting from 26 hpf, definitive HSCs (gray) emerge from hemogenic endothelial cells of the dorsal aorta in the aorta-gonad-mesonephros (AGM) region. Shortly thereafter, HSCs migrate to and seed the caudal hematopoietic tissue at 48 hpf, which is an expansion of the PBI and acts as a transient hematopoietic site that gives rise to erythroid, myeloid and thromboid (yellow) cells. The caudal hematopoietic tissue is equivalent to mouse fetal liver or placenta. HSCs from the AGM region colonize kidney around 48 hpf. Kidney marrow, which is functionally similar to mammalian bone marrow, gives rise to all blood lineages, including erythroid, myeloid, thromboid and lymphoid (green) cells for the larval and adult zebrafish. At around 54 hpf, common lymphoid progenitor (CLP) cells from the AGM region seed the thymus, which is the site for maturation of lymphoid T cells. (B) Crucial genes during different stages of hematopoietic development in zebrafish. The names of corresponding available zebrafish mutants are shown in parenthesis; the mutated genes are unknown for the mutants preceded by ‘?’. Adapted from Chen and Zon (Chen and Zon, 2009) and Paik and Zon (Paik and Zon, 2010), with permission. Lili Jing, and Leonard I. Zon Dis. Model. Mech. 2011;4:433-438 © 2011. Published by The Company of Biologists Ltd