Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2019 May;13(2):238-242.
doi: 10.1055/s-0039-1694697. Epub 2019 Sep 11.

Xerostomia Therapy Due to Ionized Radiation Using Preconditioned Bone Marrow-Derived Mesenchymal Stem Cells

Affiliations

Xerostomia Therapy Due to Ionized Radiation Using Preconditioned Bone Marrow-Derived Mesenchymal Stem Cells

Sri Wigati Mardi Mulyani et al. Eur J Dent. 2019 May.

Abstract

Objectives: The aim of this study was to describe the process of regeneration of damaged salivary glands due to ionizing radiations by bone marrow mesenchymal stem cells (BM-MSCs) transplantation that have been given hypoxic preconditioning with 1% O2 concentration.

Materials and methods: Stem cell culture was performed under normoxic (O2: 21%) and hypoxic conditions by incubating the cells for 48 hours in a low oxygen tension chamber consisting of 95% N2, 5% CO2, and 1% O2. Thirty male Wistar rats were divided into four groups: two groups of control and two groups of treatment. A single dose of 15 Gy radiation was provided to the ventral region of the neck in all treatment groups, damaging the salivary glands. BM-MSCs transplantation was performed in the treatment groups for normoxia and hypoxia 24-hour postradiation.

Statistical analysis: Statistical analysis was done using normality test, followed by MANOVA test (p < 0.05).

Results: There was a significant difference in the expression of binding SDF1-CXCR4, Bcl-2 (p < 0.05) and also the activity of the enzyme α-amylase in all groups of hypoxia.

Conclusion: BM-MSCs transplantation with hypoxic precondition increases the expression of binding SDF1-CXCR4, Bcl-2 that contributes to cell migration, cell survival, and cell differentiation.

PubMed Disclaimer

Conflict of interest statement

None declared.

Figures

Fig. 1
Fig. 1
Comparison of CXCR4 (brown chromogen) expression between treatments. In the slide it appears that hypoxic group in acute conditions showed mainly CXCR4 expression ( A ) that was stronger than that in the normoxic group ( B ). Immunohistochemical staining, 400× magnification; Nikon H600L microscope; 300-megapixel camera DS Fi2.
Fig. 2
Fig. 2
Microscopic images of BM-MSCs labeled using PKH 26. The green light in the image shows the distribution of labeled BM-MSCs. Hypoxic condition ( A ) , normoxic condition ( B ).
Fig. 3
Fig. 3
Comparison of the expression of Bcl-2 (brown chromogen) between treatments. In the slide, it appears that groups with acute hypoxia ( A ) showed stronger Bcl-2 expression compared with those in the acute normoxic group ( B ) . Immunohistochemical staining, 400× magnification; Nikon H600L microscope; 300-megapixel camera DS Fi2.

References

    1. Chambers M S, Garden A S, Kies M S, Martin J W. Radiation-induced xerostomia in patients with head and neck cancer: pathogenesis, impact on quality of life, and management. Head Neck. 2004;26(09):796–807. - PubMed
    1. Lombaert I M, Brunsting J F, Wierenga P K. Rescue of salivary gland function after stem cell transplantation in irradiated glands. PLoS One. 2008;3(04):e2063. - PMC - PubMed
    1. Ponnaiyan D, Jegadeesan V. Comparison of phenotype and differentiation marker gene expression profiles in human dental pulp and bone marrow mesenchymal stem cells. Eur J Dent. 2014;8(03):307–313. - PMC - PubMed
    1. Sohni A, Verfaillie C M. Mesenchymal stem cells migration homing and tracking. Stem Cells Int. 2013;13:1–10. - PMC - PubMed
    1. Estrada J C, Albo C, Benguría A. Culture of human mesenchymal stem cells at low oxygen tension improves growth and genetic stability by activating glycolysis. Cell Death Differ. 2012;19(05):743–755. - PMC - PubMed