Abstract

Biomedical use of radiation is utilized in effective diagnostic and treatment tools, yet can introduce risks to healthy tissues. High energy photons used for diagnostic purposes have high penetration depth and can discriminate multiple tissues based on attenuation properties of different materials. Likewise, the ability to deposit energy at various targets within tumors make the use of photons effective treatment for cancer. Radiation focused on a tumor will deposit energy when it interacts with a biological structure (e.g. DNA), which will result in cell kill should repair capacity of the tissue be overwhelmed. Likewise, damage to normal, non-cancerous tissues is a consequence of radiation that can lead to acute or late, chronic toxicity profiles. Adipose derived stem cells (ADSCs) are mesenchymal stem cells that have been proven to have similar characteristics to bone marrow derived stem cells, except that they are much easier to obtain. Within the body, ADSCs act as immunomodulators and assist with the maintenance and repair of tissues. They have been shown to have excellent differentiation capability, making them an extremely viable option for stem cell therapies and regenerative medicine applications. Due to the tissue ADSCs are derived from, they are highly likely to be affected by radiation therapy, especially when treating tumors localized to structures with relatively high ADSC content (eg., breast cancer). For this reason, the purpose behind this research is to better understand how ADSCs are affected by doses of radiation comparable to a single fraction of radiation therapy. We also measured the response of ADSCs to exposure at different dose rates to determine if there is a significant difference in the response of ADSCs to radiation therapy relevant doses of ionizing radiation. Our findings indicate that ADSCs exposed to Cesium (Cs 137)-gamma rays at a moderate dose of 2Gy and either a low dose rate (1.40Gy/min) or a high dose rate (7.31Gy/min) slow proliferation rate, and with cell cycle arrest in some populations. These responses ADSCs were not as marked as previously measured in other stem cell types. In addition, our results indicate that differences in dose rate in the Gy/min range typically utilized in small animal or cell irradiation platforms have a minimal effect on the function of ADSCs. The potential ADSCs have in the space of regenerative medicine makes them an ideal candidate for study with ionizing radiation, as they are one of the main cell types to promote tissue healing.

Highlights

  • Exposure to ionizing radiation is unavoidable as there are plenty of natural background radiation sources and exposure through imaging sources is a standard part of modern medical practice

  • There is no statistical difference in the number of cells in culture expect for lower dose rate (LDR) at day 5 where it is significantly different from control, but not higher dose rate (HDR) irradiated samples (Fig 1)

  • At all the time points, HDR samples in G0/G1 were significantly different than both control and LDR samples, while LDR was significantly different than control at day 3 only (Fig 3b)

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Summary

Introduction

Exposure to ionizing radiation is unavoidable as there are plenty of natural background radiation sources and exposure through imaging sources is a standard part of modern medical practice. Dose rate has been directly linked to elevated lifetime risk of cancer and non-cancer disease formation [1,2]. These observations are, in part, based off the Lifespan Study (LSS) of atomic bomb survivors who were exposed to various total doses of radiation (depending on the distance from the bomb) at a very high dose rate. Depending on the location of the scan, a patient can receive between 2-20mSv over a period of several minutes [5,6], which is a considerably greater rate than observed from background radiation and has been shown to be associated with elevated cancer risk [7,8]

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