Haematopoiesis is the formation of blood cellular components. All cellular blood components During fetal development, since bones and thus the bone marrow develop later, the liver functions as the main haematopoetic organ. Therefore. hematopoyesis fetal pdf. Quote. Postby Just» Tue Aug 28, am. Looking for hematopoyesis fetal pdf. Will be grateful for any help! Top. EnglishEspañol한국어日本語DeutschPortuguêsFrançaisMagyarItaliano. Present. Create your own · Report. Hematopoyesis fetal y primitiva. LT.
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Normal development of fetal hepatic haematopoiesis during the second trimester of gestation is upregulated by fibronectin expression in the stromal cells of the portal triads. Venizelos 1S. General Hospital of Chania. Democritus University of Thrace. In hematopoietic organs, stromal cells such as fibroblasts, epithelial cells, and macrophage-like cells develop networks to maintain hematopiyesis, i.
HEMATOPOYESIS – Definition and synonyms of hematopoyesis in the Spanish dictionary
ECM glycoproteins produced by the stromal cells are hematopoyessi to play a critical role in the regulation of cell growth and differentiation. Numerous soluble and membrane-bound factors directly regulating haematopoiesis have been documented, but little is known about fetal hepatic stromal cell activity and stromal extracellular matrix protein-fibronectin, on fetal hepatic haematopoiesis.
The binding of late stage erythroid cells to fibronectin has been well characterized and is believed to be critical for the terminal stages of erythroid differentiation. The intention of this article is to determine the role of fibronectin in fetal hepatic hematopoietic proliferation and differentiation in different stages of development.
Seconda trimester of gestation. Fibronectin FN is a multidomain adhesive glycoprotein found in blood and hematppoyesis connective tissue. It interacts with multiple cell surface receptors and plays an important role in the regulation of anchorage-dependent cell growth, cell migration, differentiation, gene expression, tumor development and metastasis, embryogenesis, angiogenesis, and wound healing Feta reason why the liver is the major haematopoietic site during fetal life is not clear.
That the bone marrow is not yet mature this period and that fetal hematopoietic stem cells HSCs present specific characteristics do not explain the specific HSC homing to the fetal liver tissue. Stromal cells of the hepatic stromal triads synthesize growth factors, cell adhesion molecules, and extracellular matrix ECM molecules which are essential for the establishment of a microenvironment supportive of haematopoietic cell growth and differentiation 6.
Fibronectin, a multifunctional ECM glycoprotein found in the fetal hepatic parenchyme hepatic stromal cellshas been shown to influence the adhesion, migration, growth, and differentiation of many cell types, including hematopoietic cells 7.
Interactions of erythroid cells with FN are believed to hemstopoyesis essential for erythropoiesis, particularly for the terminal stages of erythroid differentiation 8. Human haematopoiesis is initiated in the yolk sac during fstal 3rd week of development 9.
These cells form compact clusters in close association with the ventral wall of the dorsal aorta 9,10 and then eventually seed in the fetal liver and spleen In contrast, haematopoiesis in the bone marrow commences only about the 12th week of gestation 9. The liver becomes the predominant haematopoietic site from the 6th week of gestation.
Bone marrow takes over after birth. Erythropoiesis comprises hsmatopoyesis major part of fetal liver hemopoieisis. Most studies performed by light and electron microscopy have shown early development of erythropoiesis in hepatocyte “niches”, with continuing maturation within the sinusoids.
Cells of erythroid lineage are present in circumscribed clusters in the hepatic parenchyma, which is the place of early erythropoietic development and along the sinusoids where further maturation takes place. Myelomonocytic cells, during the first trimester of gestation, are located mostly in the mesenchymal tissue of the portal triads.
In the second trimester the distribution pattern is somewhat different. No main localization is seen in portal spaces, but scattered cells in liver parenchyma and sinusoids are visible. Lymphoid cells are present in small numbers in all stages. These cells are partly scattered throughout the sinuses but, surprisingly, from 16 week onwards, a considerable number of lymphoid cells are also observed in the perivascular connective tissue in the portal triads and around the central veins, which is similar to the localization of myelopoiesis.
The availability of a broad range of monoclonal antibodies Mabs recognizing antigens present on cells of different haemopoietic lineages has extended the possibilities for an accurate description of the cells present in these separate lineages and their precursors during different stages of human embryonic and fetal development.
CD34 antigen is a single chain transmembrane glycoprotein with a molecular weight of KD. The CD34 protein is selectively expressed on human lymphoid and myeloid haematopoietic progenitor cells.
The CD34 protein is also expressed on vascular endothelium. Our study gives insight into mechanisms of augmentation of hepatic hematopoiesis with fibronectin expression during the second trimester of development.
We studied 15 cases of hepatic fetal specimens in different stages of development 1 st2 ndand 3 rd trimester obtained after voluntary abortion due to leiomyoma five samplesto implantation of the fetus in the region of the internal os resulting in placenta previa six samplesand to endometriosis-adenomyosis four samples.
All cases were chosen from specific time of development 2 nd month: The study was executed in harmony with the guidelines for the analysis of fetal cells and tissues and approved by the Ethics Committee of the General Hospital of Alexandroupolis. Detection of the antigens in formalin-fixed tissue specimens required antigen-demasking protocols prior to application of antibodies. In most instances this was accomplished using high-pressure cooking 11 in 10 mM citrate buffer at pH 6.
Specifically bound antibodies were made visible with the alkaline phospatase-anti-alkaline phosphatase APAAP technique 12 using FastRed as chromogen. The immunostained sections were examined with a X 40 objective and the distribution of fibronectin and NCL-END within the cell was recorded.
hematopoyesis fetal pdf
Every stained cell was scored as positive regardless of staining intensity. To count the number of cells with fibronectin and CD34 stainings, a 10 X 10 square calibrated grid was inserted into the eyepiece of an Olympus BX40 binocular microscope. Five-to-ten fields were examined for each section, and at least 1, cells were scored, depending on cellularity.
The percentage of positive cells was recorded as the relevant indices. The mean index was evaluated in three ranges: Hepatic portal triad stromal cells expressed fibronectin in 7 of 15 fetuses-cases during the first trimester Progenitor hematopoietic cells, stromal progenitor cells, and vascular endothelial cells expressed CD34 in 10 of 15 fetuses-cases during the first trimester Of 7 fetuse-cases with positive fibronectin expression during the first trimester, 5 were scored as grade I, and 2 as grade III.
Of 15 fetuse-cases with positive fibronectin expression during the second trimester, 4 were scored as grade I, 9 as grade II, and 2 as grade III. Immunohistochemical control for fibronectin is shown in figure 1; there is a strong reactivity with the stromal cells of the hepatic portal triads. Of 8 fetuse-cases with positive fibronectin expression during the third trimester, 4 were scored as grade I, 2 as grade II, and 2 as grade III. Immunohistochemical control for CD34 is shown in figure 2: Over the years, several models have been advanced proposing that haematopoietic lineage determination is driven extrinsically through growth factors, stroma or other external influences 13intrinsically as described in stochastic models 14,15or both 16, Within the haematopoietic microenvironment, early progenitors are maintained in specific compartmentalized niches, where they interact with other cell types and components of the extracellular matrix 18, The microenvironment has been reported to influence survival, proliferation, and differentiation 20, More recently, it has been suggested that the primary function of these extrinsic signals, including growth factors, is to support the survival and development of committed cells, whereas lineage commitment can be attributed to cell intrinsic mechanisms 14,15,17, Overall, it appears that the regulation of haematopoiesis is the result of multiple processes involving cell-cell and cell-extracellular matrix interactions, the action of specific growth factors and other cytokines, as well as intrinsic modulators of haematopoietic development.
In most cells, adhesion is an essential process in the control of growth and differentiation and, although hematopoietic progenitor cells can grow in suspension and therefore can bypass this requirement, they have a close association with their stromal extracellular matrix which, under physiological conditions, may regulate interactions with locally available growth factors.
Blood cell formation is controlled by a complex set of events, including interactions between ECM and hematopoietic cells Multiple cell types interact within a confined space in hematopoietic organs to deliver and receive critical signals for proliferation and differentiation.
Therefore, FN seemed to promote colony formation of both committed and uncommitted progenitors, and these effects of FN were seen on a wider stage of differentiation than that reported by Weinstein et al.
Several studies have shown that ligation of FN to integrins stimulate a variety of signaling events, including tyrosine phosphorylation, cytoplasmic alkalization, calcium influx, accumulation of cytoskeletal molecules at sites of hematopoyesjs adhesion, and altered gene expression Attachment of epithelial and endothelial cells to ECM is essential for their survival both in vitro and in vivo because they undergo apoptosis by the inhibition of these interactions In addition, several lines of evidence suggest that signal transduction events through integrin ligand engagement are involved in the suppression of apoptosis in anchored cells.
For example, attachment of fetla to ECM via integrins regulated expression of interleukin 1 beta IL-1b converting enzyme, a protein associated with apoptosis Apoptosis of detached endothelial cells was suppressed by the addition of sodium vanadate, a protein tyrosine phosphatase inhibitor Moreover, injection of an anti-ppFAK antibody into rounded fibroblasts resulted in the rapid onset of apoptosis.
It is also known that ppFAK directly associates with b subunit of integrins, and its tyrosine phosphorylation and kinase activity are upregulated by the binding of FN to integrins Further analysis will be necessary to reveal the signal transduction pathway and structural basis of FN for promoting cell survival and growth. All types of hemopoietic cells derive from a small pool of immature uncommitted progenitor cells. During the past few decades the phenotype of the hemopoietic progenitors has been analyzed in detail.
This antigen is expressed on almost all types of hemopoietic progenitors. However, CD34 is also expressed on stromal cell progenitors and even on vascular endothelium. Fibronectin, one of vetal components of ECM molecules, plays an important role in the regulation of hematopoietic differentiation. The mechanism s of action of fibronectin on hematopoietic stem cell and microenvironment remain to be determined; however, fibronectin may possibly act by increasing binding of hematopoietic cells to stromal cells and by increasing the utilization feyal hematopoietic growth factors by the stem cells cooperating with other ECM molecules.
Our results imply that the expression of fibronectin in higher amounts during the second trimester of gestation provides evidence that this specific extracellular matrix glycoprotein induces the hemopoietic progenitor cell proliferation and differentiation in the fetal liver.
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