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1.
Journal of Experimental Hematology ; (6): 490-494, 2015.
Article in Chinese | WPRIM | ID: wpr-259559

ABSTRACT

<p><b>OBJECTIVE</b>This study was to construct the lentivirus vector carrying hepatocyte growth factor (HGF) gene and to explore the condition for transfecting the adipocyte-derived mesenchymal stem cells (ADSC) by HGF lentivirus.</p><p><b>METHODS</b>The target gene was obtained from plasmid carrying HGF gene by PCR and was cloned into GV287 vector. The recombinant GV287-HGF vector plasmid and lentivirus-packing plasmid were co-transfected into 293 T cells to generate HGF lentivirus, and the virus titer was assayed, then the ADSC were transfected by using recombinant HGF lentivirus, and the optimal multplicity of infection (MOI) was detected.</p><p><b>RESULTS</b>The PCR product of HGF gene was consistent with expectant sizes, suggesting that the electrophoretic result of recombinant GV287-HGF plasmid PCR product was correct. The sequencing analysis of cleaved product showed consistance of obtained results with the sequences of target gene, suggesting correct construction of recombinant lentivirus carrying HGF gene. The ELISA showed that the virus tilter was 5×10(8) TU/ml. The optimal MOI for transfecting ADSC with recombinant lentivirus carrying HGF gene was 50.</p><p><b>CONCLUSION</b>The lentivirus vector expressing human HGF gene has been constructed, and transfected the ADSC succesfully. This study lays a foundation for further stadying the ADSC over-expressioning HGF, treating the radiation damage of bone marrow and impartant internal organs.</p>


Subject(s)
Animals , Humans , Rats , Adipocytes , Cell Line , Gene Expression , Genetic Vectors , Hepatocyte Growth Factor , Lentivirus , Mesenchymal Stem Cells , Plasmids , Transfection
2.
Journal of Experimental Hematology ; (6): 1774-1779, 2015.
Article in Chinese | WPRIM | ID: wpr-272523

ABSTRACT

Transfusion-associated graft-versus-host disease (TA-GVHD) is a rare complication of blood transfusion. The disease is fulminant and fatal in most patients. TA-GVHD is caused by transfused alloreactive donor T lymphocytes that attack host tissue, including skin, liver, gastrointestinal tract and bone marrow. Most patients are immunocompromised, but immunocompetent patients can also be involved. Irradiation of blood components is generally recommended to prevent the onset of TA-GVHD for susceptible recipients. This review focus on pathogenesis and prevention of TA-GVHD.


Subject(s)
Humans , Blood Transfusion , Bone Marrow , Gastrointestinal Tract , Graft vs Host Disease , Liver , T-Lymphocytes , Tissue Donors
3.
Journal of Experimental Hematology ; (6): 1142-1147, 2014.
Article in Chinese | WPRIM | ID: wpr-302331

ABSTRACT

A disintegrin-metalloproteinase 28 (ADAM28) is one of important members of ADAM family, that is involved in various biological events including cell adhesion, proteolysis, growth and metastasis of solid tumors and hematological malignancies. Studies have shown that ADAM28 is highly expressed in several human tumors, such as lung, breast and bladder cancers, and chronic lymphocytic leukemia, and its tissue expression levels correlate with cancer metastasis. ADAM28-mediated cancer cell metastasis may be related with the cleavage of von Willebrand's factor (vWF), insulin-like growth factor binding protein-3 (IGFBP-3) and connective tissue growth factor (CTGF), as well as the promoting PSGL-1/P-selectin-mediated cell adhesion. This review summarizes the basic and translational aspects of ADAM28 biology that might stimulate the interest in ADAM28 research and discovery of novel ADAM28 targets, providing potential novel therapies for metastatic cancers.


Subject(s)
Humans , ADAM Proteins , Metabolism , Cell Adhesion , Connective Tissue Growth Factor , Metabolism , Insulin-Like Growth Factor Binding Protein 3 , Metabolism , Neoplasm Metastasis , Neoplasms , Pathology , von Willebrand Factor , Metabolism
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