|
|
| (5 intermediate revisions by 2 users not shown) |
| Line 1: |
Line 1: |
| __NOTOC__ | | __NOTOC__ |
| {{SI}} | | {{Hematopoeisis}} |
| {{CMG}} | | {{CMG}} |
|
| |
|
| ==Overview== | | ==[[Hematopoiesis overview|Overview]]== |
|
| |
|
| '''Haematopoiesis''' (from Ancient Greek: ''haima'' blood; ''poiesis'' to make) (or '''hematopoiesis''' in the United States; sometimes also '''haemopoiesis''' or '''hemopoiesis''') is the formation of [[blood]] cellular components. All of the cellular components of the blood are derived from [[haematopoietic stem cell]]s. The term multipotent refers to the ability of a cell to become several different types of cell (but not all types in a germ layer). Multipotent haematopoietic cells can become any type of cell in the blood system. The multipotent cells determine what type of cell to become, or differentiate, in a step-wise fashion. It normally goes at a speed of 10<sup>11</sup>–10<sup>12</sup> cells per day <ref name=T4> Semester 4 medical lectures at Uppsala University 2008 by Leif Jansson</ref>
| | ==[[Hematopoiesis lineages|Lineages]]== |
|
| |
|
| [[Image:Hematopoiesis simple.jpg|thumb|left|400px|Simple diagram that shows the development of different blood cells from hematopoietic stem cell to mature cells]] | | ==[[Hematopoiesis locations|Locations]]== |
| <br clear="left"/>
| |
|
| |
|
| ==Lineages== | | ==[[Hematopoiesis maturation|Maturation]]== |
|
| |
|
| All blood cells are divided into three lineages.
| | ==Related Chapters== |
| * [[erythrocyte|Erythroid]] cells are the [[oxygen]] carrying [[red blood cells]].
| |
| * [[Lymphoid]] cells are the cornerstone of the adaptive immune system. They are derived from common lymphoid progenitors. The lymphoid lineage is primarily composed of [[T-cell]]s and [[B-cell]]s. (white blood cells)
| |
| * [[Myeloid]] cells, which includes [[granulocyte]]s, [[megakaryocyte]]s, and [[macrophage]]s, are derived from common myeloid progenitors, and are involved in such diverse roles as [[innate immunity]], [[adaptive immunity]], and [[blood clotting]].
| |
| | |
| [[Image:Hematopoiesis (human) diagram.png|thumb|left|400px|Comprehensive diagram that shows the development of different blood cells from hematopoietic stem cell to mature cells]]
| |
| <br clear="left"/>
| |
| ===Granulopoiesis=== | |
| Granulopoiesis (or granulocytopoiesis) is hematopoiesis of [[granulocytes]].
| |
| | |
| It occurs primarily within [[bone marrow]].
| |
| | |
| It involves the following stages:
| |
| | |
| * [[Pluripotential hemopoietic stem cell]]
| |
| * [[Myeloblast]]
| |
| * [[Promyelocyte]]
| |
| * [[Eosinophilic myelocyte|Eosino]]/[[neutrophilic myelocyte|neutro]]/[[basophilic myelocyte]]
| |
| * [[Metamyelocyte]]
| |
| * [[Band cell]]
| |
| * [[Granulocytes]] ([[Eosinophil|Eosino]]/[[neutrophil|neutro]]/[[basophil]])
| |
| | |
| ==Locations==
| |
| In developing embryos, blood formation occurs in aggregates of blood cells in the yolk sac, called [[blood islands]]. As development progresses, blood formation occurs in the [[spleen]], [[liver]] and [[lymph node]]s. When [[bone marrow]] develops, it eventually assumes the task of forming most of the blood cells for the entire organism. However, maturation, activation, and some proliferation of lymphoid cells occurs in secondary lymphoid organs ([[spleen]], [[thymus]], and [[lymph node]]s). While most haematopoiesis in adults occurs in the marrow of the long bones such as the [[femur]]s, it also occurs in spongy bone like [[rib]]s and [[sternum]]).
| |
| | |
| ===Extramedullary=== <!--Extramedullary hematopoiesis redirects here-->
| |
| In some cases, the [[liver]], [[thymus]], and [[spleen]] may resume their haematopoietic function, if necessary. This is called ''extramedullary haematopoiesis''. It may cause these organs to increase in size substantially. <ref name=T4> Semester 4 medical lectures at Uppsala University 2008 by Leif Jansson</ref>
| |
| | |
| ===Other vertebrates===
| |
| In some [[vertebrate]]s, haematopoiesis can occur wherever there is a loose [[stroma]] of connective tissue and slow blood supply, such as the [[gut]], [[spleen]], [[kidney]] or [[ovaries]].
| |
| | |
| ==Maturation==
| |
| As a stem cell matures it undergoes changes in gene expression (the extent by which a gene exerts influence on its target changes) that limit the cell types that it can become and move it closer to a specific cell type. These changes can often be tracked by monitoring the presence of proteins on the surface of the cell. Each successive change moves the cell closer to its final choice of cell type and further limits its potential cell type until it is fully differentiated. This process is usually presented as a [[dendrogram]] or decision tree, which starts with a stem cell at the single starting point, and branches for the major lineages that branch into intermediate semi-differentiated cell types, and eventually, to fully differentiated cells.
| |
| | |
| === Determination ===
| |
| It seems like it's the location of blood cells that makes the cell determination and not vice versa (i.e. e.g. that a [[hematopoietic stem cell]] determined to differentiate into a specific cell type would end up at a destined location). For instance, the [[thymus]] provides an environment for thymocytes to differentiate into a variety of different functional T cells.
| |
| | |
| For the stem cells and other undifferentiated blood cells in the [[bone marrow]], the determination is generally explained by the ''determinism'' theory of hematopoiesis, saying that colony stimulating factors and other factors of the hematopoietic microenvironment determine the cells to follow a certain path of cell differentiation. This is the classical way of describing hematopoiesis. In fact, however, it is not really true. The ability of the [[bone marrow]] to regulate the quantity of different cell types to be produced is more accurately explained by a ''stochastic'' theory: Undifferentiated blood cells are determined to specific cell types by randomness. The hematopoietic microenvironment avails some of the cells to survive and some, on the other hand, to perform [[apoptosis]]. By regulating this balance between different cell types, the [[bone marrow]] can alter the quantity of different cells to ultimately be produced.
| |
| | |
| === Haematopoietic growth factors ===
| |
| | |
| Red and white blood cell production is regulated with great precision in healthy humans, and the production of granulocytes is rapidly increased during infection. The proliferation and self-renewal of these cells depend on stem cell factor (SCF).
| |
| Glycoprotein growth factors regulate the proliferation and maturation of the cells that enter the blood from the marrow, and cause cells in one or more committed cell lines to proliferate and mature.
| |
| Three more factors which stimulate the production of committed stem cells are called [[colony-stimulating factors]] (CSFs) and include [[granulocyte-macrophage CSF]] (GM-CSF), [[granulocyte CSF]] (G-CSF) and [[macrophage CSF]] (M-CSF).
| |
| These stimulate a lot of [[granulocyte]] formation. They are active on either [[progenitor cells]] or end product cells.
| |
| | |
| [[Erythropoietin]] is required for a myeloid progenitor cell to become an erythrocyte. <ref name=lodish>Molecular cell biology. Lodish, Harvey F. 5. ed. : - New York : W. H. Freeman and Co., 2003, 973 s. b ill. ISBN 0-7167-4366-3</ref> On the other hand, [[thrombopoietin]] makes myeloid progenitor cells differentiate to [[megakaryocytes]] ([[thrombocyte]]-forming cells).<ref name=lodish/>
| |
| | |
| Examples of cytokines and the blood cells they give rise to, is shown in the picture below.
| |
| | |
| [[Image:Hematopoiesis (human) cytokines.jpg|thumb|500px|left|Diagram including some of the important cytokines that determine which type of blood cell will be created.<ref name=lodish/>
| |
| SCF= [[Stem Cell Factor]]
| |
| Tpo= [[Thrombopoietin]]
| |
| IL= [[Interleukin]]
| |
| GM-CSF= [[Granulocyte Macrophage-colony stimulating factor]]
| |
| Epo= [[Erythropoietin]]
| |
| M-CSF= [[Macrophage-colony stimulating factor]]
| |
| G-CSF= [[Granulocyte-colony stimulating factor]]
| |
| SDF-1= [[Stromal cell-derived factor-1]]
| |
| FLT-3 ligand= FMS-like tyrosine kinase 3 ligand
| |
| TNF-a = [[Tumor necrosis factor-alpha]]
| |
| TGFβ = [[Transforming growth factor]] beta
| |
| ]]
| |
| <br clear="left"/>
| |
| | |
| === Transcription factors ===
| |
| Growth factors initiate [[signal transduction]] pathways, altering [[transcription factors]], that, in turn activate genes that determines the differentiation of blood cells.
| |
| | |
| The early committed progenitors express low levels of transcription factors that may commit them to discrete cell lineages. Which cell lineage is selected for differentiation may depend both on chance and on the external signals received by progenitor cells.
| |
| Several transcription factors have been isolated that regulate differentiation along the major cell lineages. For instance, PU.1 commits cells to the myeloid lineage whereas GATA-1 has an essential role in erythropoietic and megakaryocytic differentiation.
| |
| | |
| '''Extramedullary hematopoiesis in a thalassemia patient'''
| |
| <gallery>
| |
| Image:
| |
| | |
| Extramedullary-hematopoiesis-001.jpg
| |
| | |
| Image:
| |
| | |
| Extramedullary-hematopoiesis-002.jpg
| |
| | |
| Image:
| |
| | |
| Thalassemia-101.jpg
| |
| | |
| Image:
| |
| | |
| Thalassemia-102.jpg
| |
| | |
| </gallery>
| |
| | |
| ==See also==
| |
| *[[Granulopoiesis]], the hematopoiesis of granulocytes. | | *[[Granulopoiesis]], the hematopoiesis of granulocytes. |
|
| |
| ==References==
| |
| {{reflist}}
| |
|
| |
| ==External links==
| |
| * {{eMedicineDictionary|granulopoiesis}}
| |
| * {{GPnotebook|-1838481350}}
| |
| * [http://www.som.tulane.edu/classware/pathology/Krause/Blood/GP.html Overview at tulane.edu]
| |
|
| |
|
| {{Immune system}} | | {{Immune system}} |