مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Verion

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

497
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

0
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

Investigation of rat bone marrow mesenchymal stem cells effect on apoptosis and cell surface markers expression of CD33 and CD34 as an approach to treatment of chronic myeloid leukemia

Pages

  210-225

Abstract

 Background and Objectives Drug resistance is one of the main challenges in the treatment of chronic myeloid leukemia (CML). In this study, with the aim of inducing Apoptosis in K562 cell line (CML), this cell line was Co-cultured with rat bone marrow mesenchymal stem cells (rBMSCs). Then, the rate of Apoptosis as well as cell surface markers expression of CD33 and CD34 in the K562 cells line was evaluated. Materials and Methods In this experimental study, after isolating rBMSCs, the multilineag differentiation capacity of rBMSCs as well as the mesenchymal stemness of these cells was identified by evaluation of CD90, CD105, CD45, and CD56 cell surface. Then, the K562 cells were subjected for evaluation of CD33 and CD34 cell surface markers and Apoptosis using a flow cytometry technique. Results Immunophenotyping of the cells indicated positive expression of CD90 and CD105 and negative expression of CD45 and CD56. The expression of CD33 and CD34 cell markers in the K562 cell line was increased 45. 2% and 76. 5%, respectively. Also, induction of Apoptosis in the K562 cell line significantly increased (56. 6%) compared to the control (p < 0. 05). Conclusions Briefly, this study showed that the co-culturing of the K562 cells line with rBMSCs causes significant increase in the expression of CD33 and CD34 cell surface markers as well as induction of Apoptosis in the K562 cells (p < 0. 05). This effect can be through the secreted factors and cytokines of rBMSCs; however, better evaluation in terms of type of cytokines is recommended in the future studies.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    NAJAFI, D., FATHI, E., & FARAHZADI, R.. (2018). Investigation of rat bone marrow mesenchymal stem cells effect on apoptosis and cell surface markers expression of CD33 and CD34 as an approach to treatment of chronic myeloid leukemia. THE SCIENTIFIC JOURNAL OF IRANIAN BLOOD TRANSFUSION ORGANIZATION (KHOON), 15(3 ), 210-225. SID. https://sid.ir/paper/78783/en

    Vancouver: Copy

    NAJAFI D., FATHI E., FARAHZADI R.. Investigation of rat bone marrow mesenchymal stem cells effect on apoptosis and cell surface markers expression of CD33 and CD34 as an approach to treatment of chronic myeloid leukemia. THE SCIENTIFIC JOURNAL OF IRANIAN BLOOD TRANSFUSION ORGANIZATION (KHOON)[Internet]. 2018;15(3 ):210-225. Available from: https://sid.ir/paper/78783/en

    IEEE: Copy

    D. NAJAFI, E. FATHI, and R. FARAHZADI, “Investigation of rat bone marrow mesenchymal stem cells effect on apoptosis and cell surface markers expression of CD33 and CD34 as an approach to treatment of chronic myeloid leukemia,” THE SCIENTIFIC JOURNAL OF IRANIAN BLOOD TRANSFUSION ORGANIZATION (KHOON), vol. 15, no. 3 , pp. 210–225, 2018, [Online]. Available: https://sid.ir/paper/78783/en

    Related Journal Papers

    Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button