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:

474
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

251
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

MESENCHYMAL STEM CELLS FROM MURINE AMNIOTIC FLUID AS A MODEL FOR PRECLINICAL INVESTIGATION

Author(s)

 BAGHABAN ESLAMINEJAD MOHAMADREZA | JAHANGIR SHAHRBANOO | AGHDAMI NASSER | Issue Writer Certificate 

Pages

  96-103

Abstract

 Background: Despite the suitability of a mouse model for preclinical investigations; little is known regarding MESENCHYMAL STEM CELLS derived from murine amniotic fluid. This is the subject of the present study.Methods: Amniotic fluid was collected from NMRI mice during the second weeks of pregnancy and plated. The cells that adhered to the culture surfaces were propagated with three successive subcultures and then characterized. To determine the differentiation potential, the cells were cultivated under osteogenic, adipogenic, and chondrogenic conditions, and followed by specific staining and RT-PCR analysis for differentiation. The proliferative potential of the cells were measured with clonogenic assays, population doubling time and number and by growth curve plotting. Cellular aging was investigated with the senescenceassociated  b-galactosidase staining method.Results: The AMNIOTIC UID primary cell culture was composed of round attened and fibroblastic cells. The latter dominated the culture after several passages. Successful tripotent differentiation of the isolated cells into BONE, cartilage and adipose cells were indicative of their MESENCHYMAL STEM CELLS nature. The isolated cells appeared to be relatively proliferative cells as confirmed by the population doubling time value which was equal to about 69 hours. Furthermore, the cells were relatively clonogenic and they tended to initiate PROLIFERATION immediately after plating (there was no lag phase in their growth curve) . b-galactosidase positive cells were first observed at passage 3 and increased in number with subsequent passages.Conclusions: Collectively it was concluded that murine amniotic fluid contained MESENCHYMAL STEM CELLS with relatively high PROLIFERATION property and typical tripotent differentiation potential.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    BAGHABAN ESLAMINEJAD, MOHAMADREZA, JAHANGIR, SHAHRBANOO, & AGHDAMI, NASSER. (2011). MESENCHYMAL STEM CELLS FROM MURINE AMNIOTIC FLUID AS A MODEL FOR PRECLINICAL INVESTIGATION. ARCHIVES OF IRANIAN MEDICINE, 14(2), 96-103. SID. https://sid.ir/paper/280654/en

    Vancouver: Copy

    BAGHABAN ESLAMINEJAD MOHAMADREZA, JAHANGIR SHAHRBANOO, AGHDAMI NASSER. MESENCHYMAL STEM CELLS FROM MURINE AMNIOTIC FLUID AS A MODEL FOR PRECLINICAL INVESTIGATION. ARCHIVES OF IRANIAN MEDICINE[Internet]. 2011;14(2):96-103. Available from: https://sid.ir/paper/280654/en

    IEEE: Copy

    MOHAMADREZA BAGHABAN ESLAMINEJAD, SHAHRBANOO JAHANGIR, and NASSER AGHDAMI, “MESENCHYMAL STEM CELLS FROM MURINE AMNIOTIC FLUID AS A MODEL FOR PRECLINICAL INVESTIGATION,” ARCHIVES OF IRANIAN MEDICINE, vol. 14, no. 2, pp. 96–103, 2011, [Online]. Available: https://sid.ir/paper/280654/en

    Related Journal Papers

  • No record.
  • 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