Author/Authors :
Tahmasbi، Mohammad Hossein نويسنده Cellular and Molecular Research Centre, Tehran University of Medical sciences (TUMS), Tehran, Iran. Tahmasbi, Mohammad Hossein , Shafiee، Mohammad نويسنده Omics Research Center, Golestan University of Medical Sciences, Gorgan, Iran. Shafiee, Mohammad , Joghataei، Mohammad Taghi نويسنده Department of Anatomy, Cellular and Molecular Research Center, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran , , Yazdanparast، Seyed Amir نويسنده Cellular and Molecular Research Centre, Tehran University of Medical sciences (TUMS), Tehran, Iran. Yazdanparast, Seyed Amir , Moosavi، Seyed Akbar نويسنده Department of Allied Health, Tehran University of Medical Sciences (TUMS), Tehran, Iran. Moosavi, Seyed Akbar , Jafarabadi، Mina نويسنده , , Soleimani، Masoud نويسنده ,
Abstract :
Background and Aim: The key role of chemokine receptor CXCR4 in the
maintenance of stemness property of stem cells has been shown recently. The low
level laser irradiation (LLLI) is being used currently in a wide variety of clinical
cases as a therapeutic tool for wound healing, relieving pain and destroying tumor
cells. The aim of this study was to evaluate the effect of LLLI mimicking low
level laser therapy (LLLT) on the expression level of CXCR4 gene a few hours
after irradiation on human blastocysts.
Methods: After the development of human embryos to the first grade blastocyst
stage, they were irradiated with a low power Ga-Al-As laser at a continuous
wavelength of 650 nm and a power output of 30 mW. Total RNA of the irradiated
blastocysts and control groups was isolated in groups of 1x2 J/cm2, 2x2 J/cm2, 1x4
J/cm2 and 2x4 J/cm2 LLLI. Specific real-time PCR primers were designed to
amplify all the two CXCR4 isoforms yet identified. RNA amplifications were
done for all groups.
Results: We showed for the first time that LLLI makes the human blastocysts to
increase the expression level of CXCR4 a few hours after irradiation. Moreover, it
was shown that two irradiation doses with one day interval can cause a significant
increase in CXCR4 expression level in human blastocysts.
Conclusion: This study revealed that LLLI could be a proliferation motivator for
embryonic cell divisions through enhanced over-expression of CXCR4 level.