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1.
Biomed Res Int ; 2018: 1082961, 2018.
Article in English | MEDLINE | ID: mdl-30622953

ABSTRACT

[This corrects the article DOI: 10.1155/2017/2597256.].

2.
Biomed Res Int ; 2017: 4284156, 2017.
Article in English | MEDLINE | ID: mdl-29209629

ABSTRACT

[This corrects the article DOI: 10.1155/2017/2597256.].

3.
Biomed Res Int ; 2017: 2597256, 2017.
Article in English | MEDLINE | ID: mdl-28791301

ABSTRACT

OBJECTIVE: To study the expressions of VEGF and VEGFR2 at protein level in the epididymis of rats with arsenism. METHODS: Forty male Sprague-Dawley rats were randomly divided into four groups: the high dose arsenic infected group (60.0 mg/L in water), the middle dose arsenic infected group (12.0 mg/L in water), the low dose arsenic infected group (2.4 mg/L in water), and the control group (distilled water). Rats were treated with arsenic through drinking water for 6 consecutive months. At the end of the experiment, the average densitometry values of apoptotic cells in epididymis tubules were determined by TUNEL method; the protein and mRNA levels of VEGF and VEGFR2 were observed by immunohistochemistry, Western blot, and real time fluorescent quantitative PCR, respectively. RESULTS: Compared with the control group, in each infected group, the average densitometry values of apoptotic cells in the epididymis tubules were significantly lower. Compared with control group, protein and mRNA levels of VEGF and VEGFR2 in each infected group were obviously declined. The correlations between protein and mRNA levels of VEGF and VEGFR2 were positively exhibited (r = 0.843, 0.869, p < 0.05). CONCLUSIONS: Arsenism affects the expressions of VEGF and VEGFR2 in the epididymis of rats and results in apoptosis of pathophysiology of male infertility.


Subject(s)
Arsenites/toxicity , Epididymis/metabolism , Sodium Compounds/toxicity , Vascular Endothelial Growth Factor A/metabolism , Vascular Endothelial Growth Factor Receptor-2/metabolism , Animals , Apoptosis/drug effects , Arsenites/poisoning , Cell Nucleus/drug effects , Cell Nucleus/metabolism , Epididymis/cytology , Epididymis/drug effects , Immunohistochemistry , Male , RNA, Messenger/genetics , RNA, Messenger/metabolism , Rats, Sprague-Dawley , Sodium Compounds/poisoning , Vascular Endothelial Growth Factor A/genetics , Vascular Endothelial Growth Factor Receptor-2/genetics
4.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-300205

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effects of total saponins from Sanguisorba officinalis (DYS) on hematopoietic cell proliferation, differentiation and the expression level of IL-3R and c-kit.</p><p><b>METHOD</b>Baf3 and 32D cells were cultured with or without IL-3, then the cells were exposed to DYS in different concentrations of 5, 10, 20, 30 and 40 mg x L(-1) for 24, 48, 72 and 96 hours separately. After that, the cell proliferation and differentiation capacity were determinated by the methods of CCK8 and Giemsa staining separately. The effects of DYS on the expression level of IL-3 receptor in Baf3 cells and the expression level of c-kit in 32D cells were determinated using RT-PCR.</p><p><b>RESULT</b>DYS promotes alone proliferation of Baf3 cells and 32D cells after 48 h. In contrast to control cells, 32D cells containing DYS without IL-3 form many large clusters. DYS also increases the proliferation when cultured with IL-3. High concentration of DYS induce alone the differentiation of 32D cells and increase alone the number of the polyploidy megakaryocyte. Moreover, DYS increases alone the expression level of IL-3R in Baf3 cells and the expression level of c-kit in 32D cells separately.</p><p><b>CONCLUSION</b>Our data shows DYS can promote alone proliferation and differentiation of megakaryocyte progenitor cells. The proliferative and differentiative effect of DYS on megakaryocyte progenitor cells is correlated to the up-regulation of IL-3 receptor and c-kit expression.</p>


Subject(s)
Animals , Mice , Cell Differentiation , Genetics , Cell Line , Cell Proliferation , Dose-Response Relationship, Drug , Gene Expression , Interleukin-3 , Pharmacology , Megakaryocyte Progenitor Cells , Metabolism , Proto-Oncogene Proteins c-kit , Genetics , Receptors, Interleukin-3 , Genetics , Reverse Transcriptase Polymerase Chain Reaction , Sanguisorba , Chemistry , Saponins , Pharmacology , Time Factors
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