key: cord-0896621-4i2x0hiw
authors: KOIKE, Manabu; YUTOKU, Yasutomo; KOIKE, Aki
title: Inhibition of Crandell-Rees Feline Kidney cell proliferation by X-ray-induced senescence
date: 2021-03-17
journal: J Vet Med Sci
DOI: 10.1292/jvms.20-0679
sha: 674256f7c2777ea71ffbf0be6fff56d85556da48
doc_id: 896621
cord_uid: 4i2x0hiw

Radioresistance and radiotoxicity have been reported following cancer treatments in felines. Optimizing radiation doses to induce cytotoxic effects to only cancer cells and not normal cells is critical in achieving effective radiation therapy; however, the mechanisms of radiation resistance, radiotoxicity, and DNA damage response (DDR) in feline cells have not yet been elucidated. A DNA double-strand break (DSB) is the most toxic type of DNA damage induced by X-rays and heavy ion beams used in treating cancers. Crandell-Rees Feline Kidney (CRFK) cells is one of the most widely used cat cells in life science research. Here, we report that DSB-triggered senescence induced by X-rays is important in inhibiting the proliferation of CRFK cells. We demonstrated through cell proliferation assay that X-rays at doses 2 Gy and 10 Gy are toxic to CRFK cells that irradiating CRFK cells inhibits their proliferation. In X-irradiated CRFK cells, a dose-dependent increase in DSB-triggered senescence was detected according to morphological changes and using senescence-associated β galactosidase staining assay. Moreover, our data indicated that in CRFK cells, the major DDR pathway, which involves the phosphorylation of H2AX at Ser139, was normally activated by ATM kinases. Our findings are useful in the understanding of X-rays-induced cellular senescence and in elucidating biological effects of radiation, e.g., toxicity, in feline cells. Furthermore, our findings suggest that the CRFK cell line is an excellent matrix for elucidating radioresistance and radiotoxicity in cat cells.

research information to elucidate the molecular mechanisms of the biological effects of radiation in cats. However, there currently are no reports on the effects and mechanisms of radiation on the proliferation of CRFK cells.

In this study, we investigated the biological effects of X-rays on the proliferation of CRFK cells. Our findings indicate that X-rays markedly suppressed the proliferation of CRFK cells. Additionally, our results suggested that the suppression of proliferation was due to increased cellular senescence triggered by the DSBs. Furthermore, we confirmed in CRFK cells that the major DDR pathway is activated normally by ATM kinases.

Cell cultures, chemicals, and X-rays CRFK cells (HSRRB, Osaka, Japan) were cultured in Dulbecco's modified Eagle's medium supplemented with 10% fetal bovine serum as previously described [17] . Adherent cells were irradiated with X-rays at 1, 2, or 10 Gy and at a dose rate of 0.71-0.77 Gy/min (200 kVp/20 mA with 0.5-mm Al and 0.5-mm Cu filters) using Pantak HF320S (Shimadzu, Kyoto, Japan) at room temperature, as described in previous studies [17] . KU-55933, an ATM kinase inhibitor, was purchased from Wako Pure Chemical (Osaka, Japan). The KU-55933, were diluted in DMSO (Sigma-Aldrich, St. Louis, MO, USA) and diluted in culture medium immediately before use.

Trypan blue exclusion test was used to determine the number of viable cells. Cells were seeded at a density of 2.2 × 10 4 cells per dish in 60-mm dishes. Next day, the cells were irradiated with X-rays and incubated for 5 days post-irradiation. Subsequently, the cells were washed with phosphate-buffered saline (PBS), suspended in Trypsin-EDTA solution (T3924, Sigma-Aldrich), collected, centrifuged, stained with 0.4 w/v% Trypan Blue Solution (Wako Pure Chemical) or 0.4% Trypan Blue (Bio-Rad, Hercules, CA, USA), and counted using TC10™ Automated Cell Counter (Bio-Rad). All irradiations were performed in triplicate.

Total protein extraction and western blot analysis were performed according to our previously described methods [11, 17] with the following modifications. The total proteins were electrophoresed on Extra PAGE One Precast Gel 5-20% (Nacalai Tesque, Kyoto, Japan) or Super Sep ACE Gel 5-20% (Wako Pure Chemical). The fractionated products were electrophoretically transferred onto Hybond-P membranes (GE Healthcare Bio-Sciences Corp., Piscataway, NJ, USA). Then, the membranes were blocked in Blocking One (Nacalai Tesque) for 60 min at room temperature and incubated with mouse anti-γH2AX monoclonal antibody (JBW301) (Upstate Biotechnology Inc., Charlottesville, VA, USA) or mouse β-actin monoclonal antibody (Sigma-Aldrich). After washing, the membranes were incubated with the anti-mouse IgG HRP-Linked Whole Ab (from sheep) (NA931) (GE Healthcare Bio-Sciences Corp.) for 60 min at room temperature. Immunoblotting was performed using Select Western Blotting Detection System (GE Healthcare Bio-Sciences Corp.). Protein bands were visualized using ChemiDoc XRS system (Bio-Rad).

Immunostaining was performed as previously described [12, 17] with the following modifications. Briefly, cultured cells were fixed in 4% paraformaldehyde for 30 min, permeabilized with 0.5% Triton X-100 in PBS for 5 min, blocked using a blocking solution, and incubated with mouse anti-γH2AX monoclonal antibody (JBW301) (Upstate Biotechnology Inc.) for 60 min at room temperature. After washing the cells with PBS, detection was performed using an Alexa Fluor 568-conjugated secondary antibody (Molecular Probes, Eugene, OR, USA) or a fluorescein isothiocyanate-conjugated secondary antibody (Cappel Laboratories, Durham, NC, USA). Then, nuclei were stained with 0.025 µg/ml of 4,6-diamino-2-phenylindole (DAPI) fluorescent dye (Boehringer Mannheim, Mannheim, Germany). Images of cells were obtained using Olympus Fluorescence Microscope BX51 (Olympus, Tokyo, Japan) equipped with a digital camera (Olympus DP50, Olympus).

For this assay, cells (5 × 10 3 ) were plated in 35-mm plates and stained using Senescence β-Galactosidase Staining Kit (Cell Signaling Technology Inc., Danvers, MA, USA) 5 days after irradiation according to the manufacturer's instructions with the following modifications. Nuclei were stained with 0.025 µg/ml of DAPI fluorescent dye. Images of the stained cells after 18 hr were obtained using Olympus CKX41 Microscope equipped with a digital camera (Olympus DP12, Olympus) or using Olympus Fluorescence Microscope BX51 equipped with a digital camera (Olympus DP50). The percentage of positively stained cells was determined by analyzing three random fields of at least 100 cells each using the Image J software. The size of cell nuclear was determined by analyzing three random fields of 10 cells each using the Image J software. All irradiations were performed in triplicate.

Cells (2.2 × 10 4 ) were plated in 60-mm plates and irradiated with X-rays on the next day. Five days after the irradiation, the cells were harvested and stained with Annexin V Alexa Fluor 488-PI-solution (Tali™ Apoptosis Kit, Invitrogen, Carlsbad, CA, USA) in accordance with the manufacturer's instructions. A 200-fold dilution of the PI staining solution was used for staining. In addition, Annexin V labeled-apoptotic cells were detected using the Tali Image-based Cytometer (Invitrogen). All irradiations were performed in triplicate.

Statistical results are presented as means ± standard deviations (n=3). Statistical analysis excluding nuclear size was performed using ANOVA and Ryan's multiple comparison tests (ANOVA4 on the WEB, https://www.hju.ac.jp/~kiriki/anova4/). Nuclear size was evaluated by Student's t-test. A P-value of less than 0.05 was considered statistically significant.

To investigate the effect of X-rays on the proliferation of CRFK cells, irradiation was performed at 2 and 10 Gy. As shown in Fig. 1 , cell proliferation was significantly inhibited in a dose-dependent manner (P<0.05). These findings indicate that the proliferation was inhibited by X-rays at both doses.

The phosphorylation of H2AX at Ser139 is one of the major and early cellular DDRs to DSBs [8, 20, 28] . γH2AX is a gold standard biomarker for DSBs [8, 20, 28] . Previously, using western blotting, we determined the change in γH2AX expression in CRFK cells between from 1 hr to 24 hr post-irradiation with X-rays at a single dose of 10 Gy [17] . As a result, the expression level of γH2AX was the highest after 1 hr [17] . To examined whether H2AX phosphorylation was induced in a dose-dependent in the total extracts from CRFK cells 1 hr post-irradiation, western blot analysis was performed with the anti-γH2AX antibody. As shown in Fig. 2A , western blot analysis indicated that the expression of γH2AX increased depending on the dose of X-rays. Next, we examined whether γH2AX focus was detected in irradiated cells by immunostaining assay using the anti-γH2AX antibody. Our results indicated that γH2AX foci were formed in the nuclei of CRFK cells at 1 hr post-irradiation (Fig. 2B ).

One of the important roles of ATM kinase or DNA-PK in DDR triggered by X-rays is to phosphorylate H2AX surrounding the DSB sites in various human and rodent cells [18, 29] ; however, such a role has not yet been investigated in cat cells, including CRFK cells. To confirm whether ATM kinase is responsible for X-ray-induced H2AX phosphorylation at Ser139 in CRFK cells, the cells were incubated in a medium containing the ATM kinase inhibitor KU-55933 (10 µM) or solvent (DMSO) for 1 hr prior to irradiation (10 Gy). As shown in Fig. 3 , the formation of γH2AX foci was inhibited in cells irradiated in the presence of KU-55933. These results suggest that ATM is the main kinase for the phosphorylation of H2AX at Ser139 induced by irradiation in CRFK cells.

To investigate whether the inhibition of CRFK cell proliferation in response to irradiation is related to senescence and apoptosis, the cells were irradiated with X-rays at 2 and 10 Gy. Firstly, 5 days after the irradiation, cells were analyzed using SA-β-gal staining, a gold standard assay for senescence. We observed senescence-specific morphologies such as a large and flat cellular shape (Fig. 4A ) and abnormal nuclei, including an enlarged-or multinucleated-nuclei (Fig. 4B) , in irradiated cells. In addition, in irradiated CRFK cells, SA-β-gal-positive cells markedly increased in a dose-dependent manner ( Fig. 4A-C) . We also quantitatively analyzed the enlarge in the size of the cell nucleus, which is another marker for senescent cells. As shown in Fig. 4D , the size of the cell nucleus was significantly larger in irradiated CRFK cells (P<0.05). Altogether, these findings indicate that X-rays highly induce senescence in CRFK cells. Next, to examine whether X-rays induced apoptosis in the irradiated CRFK cells, apoptosis was quantified using Tali™ Image-based Cytometer. Dual staining with fluorescent Annexin V and PI was performed to detect apoptotic cells. Cells stained positive for Annexin V are considered apoptotic cells. As shown in Fig. 5 , the proportion of apoptotic cells was significantly higher in the 10-Gy group than in the non-irradiated group and the 2-Gy group but was lower (approximately 6%) in the 10-Gy group. In addition, no significant increase in apoptosis was observed in the 2-Gy group compared with the non-irradiated group. 

Understanding the biological effect of radiation on cat cells is important elucidating radiotoxicity and for developing novel therapeutic protocols for cancer treatment. In the present study, we found that the proliferation of the cat kidney cell line CRFK was significantly suppressed by X-rays at doses 2 and 10 Gy. These findings reveal that X-rays are toxic to the growth of CRFK cells under the conditions used in this study. Moreover, senescent cells markedly increased in irradiated CRFK cells. Meanwhile, our findings revealed in CRFK cells, ATM kinase induces the phosphorylation of H2AX at Ser139, which is one of the major DDRs to DSBs produced by X-rays. Radiation-induced DSBs reportedly can induce senescence and apoptosis in human and rodent cells [4, 22] . Our findings suggest that the senescence mechanism activated by DSBs contributed in suppressing the proliferation of CRFK cells by X-rays.

The mechanism underlying the difference in radiosensitivity among humans, dogs and cats and the repair mechanism of cat cells have not yet been elucidated. As mentioned above, our data indicated that the ATM kinase-dependent DDR is activated by X-rays in CRFK cells. Additionally, this study and previous studies demonstrate that X-ray-induced DSBs in CRFK cells can be detected by western blot analysis and immunocytochemistry using the commercially available anti-γH2AX antibody [17] . These findings suggest that CRFK cells is useful in clarifying the molecular mechanisms of DDR in cat cells. Moor [24] described that radiation therapy for cats is different from that for dogs in terms of tumor responses and normal tissue toxicity. Fujii et al. [7] showed that the fibroblasts in cats are more radioresistant than those in humans in a colony-forming analysis and radiationinduced γH2AX foci may be repaired faster and more effectively in feline fibroblasts. In addition, they suggested the possibility that DNA and chromosome damage induced by X-rays is more effectively repaired in feline lymphocytes than in human or dog lymphocytes. These findings suggest that the differences in radioresistance among humans, dogs and cats may be is related to the difference in DNA repair ability. Recently, we demonstrated using CRFK cells that the core NHEJ repair proteins, i.e., cat Ku70, Ku80, and XLF, accumulate at DSB sites induced by the 405-nm microlaser [17] . We have also revealed that the recruitment of cat XLF, human XLF, or dog XLF is dependent on the presence of Ku [13, 14, 17] ; these findings strongly support that the spatiotemporal regulation of core NHEJ factors, including Ku70, Ku80, and XLF, is important in the regulation of NHEJ repair [10, 19] . Collectively, CRFK cells may be useful in uncovering the molecular mechanisms underlying not only the differences of radioresistance among cat, dog, and human cells but also DDRs, including Ku-dependent NHEJ repair conserved in them.

The epithelial mesenchymal transition (EMT) is an important mechanism for malignant transformation, e.g., changing the resistance of cancer cells to radiation and anticancer drugs. Recently, CRFK cells have been reported to have the characteristics of fibroblast, particularly regarding morphology, biochemistry, and molecular biology, although CRFK cells have been established as an epithelial cell line [21] . Moreover, van Beusekom et al. [31] reported that TGF-β1 changed the morphology of CRFK cells from an epithelial phenotype to a fibroblastic phenotype and that it significantly induced the expression of some EMT marker genes in CRFK cells, suggesting that CRFK cells can undergo EMT. In the present study, senescence appeared more important than apoptosis for growth suppression in irradiated CRFK cells. Altogether, CRFK cell line may be an excellent modality for not only elucidating the interrelationship between or among X-ray-induced senescence, radioresistance, and/or radiotoxicity in cat kidney epithelial cells but also for elucidating the effects of EMT against radiation and chemotherapeutics.

Pro-senescence therapy is a novel anti-cancer strategy on the basis of inducing cancer cell senescence. In order to apply this strategy to the treatment of cats, it is necessary to elucidate the molecular mechanism of senescence induction in feline cells. On the other hand, Li et al. [22] have described that senolytic agents, a class of small molecules that can selectively kill senescent cells, hold great potential to substantially reduce the side effects caused by radiotherapy while reasonably steer clear of carcinogenesis. Recently, it was shown that a senolytic agent ABT-737 eliminates ionizing radiation induced senescent cells from lung of irradiated mice [35] . As mentioned above, our data showed that senescent cells markedly increased in irradiated CRFK cells. Our findings and further studies using CRFK cells may be available for basic research for development not only of feline prosenescence therapy, but also of senolytic agents in order to reduce the side effects caused by radiotherapy.

CRFK is one of the most important mammalian cell lines and is widely used in experiments including those on viruses, such as severe acute respiratory syndrome coronavirus (SARS-CoV) or SARS-CoV-2; DNA repair and cancer research in cats; chronic kidney disease; and the production of vaccines [1, 2, 17, 30, 33, 34] . CRFK cells can be infected with various viruses, including oncoviruses [1] [2] [3] 34] . Based on these, we speculate that the CRFK cell line may be suitable for basic research on changes in radiosensitivity induced by viral infection and on the effect of radiotherapy on tumors induced by oncoviral infection. CRFK cells can be used to elucidate the mechanisms underlying radioresistance and radiotoxicity in cat kidney epithelial cells and the effect of viral infection on radiosensitivity. Conclusively, CRFK cells may be excellent cell lines for conducting research on radiotoxicity in cats and basic research for developing new cancer treatment methods.

Comparative tropism, replication kinetics, and cell damage profiling of SARS-CoV-2 and SARS-CoV with implications for clinical manifestations, transmissibility, and laboratory studies of COVID-19: an observational study

Development, characterization, and viral susceptibility of a feline (Felis catus) renal cell line (CRFK)

Living on a break: cellular senescence as a DNA-damage response

DNA-PK, ATM and ATR as sensors of DNA damage: variations on a theme?

H2AX phosphorylation at the sites of DNA double-strand breaks in cultivated mammalian cells and tissues

Comparative study of radioresistance between feline cells and human cells

DNA damage response signaling pathways and targets for radiotherapy sensitization in cancer

Sensing and repairing DNA double-strand breaks

Dimerization, translocation and localization of Ku70 and Ku80 proteins

Accumulation of Ku80 proteins at DNA double-strand breaks in living cells

Dimerization and nuclear localization of ku proteins

Accumulation of Ku70 at DNA double-strand breaks in living epithelial cells

Cloning, localization and focus formation at DNA damage sites of canine XLF

Cloning, localization and focus formation at DNA damage sites of canine Ku70

Cloning of canine Ku80 and its localization and accumulation at DNA damage sites

Feline XLF accumulates at DNA damage sites in a Ku-dependent manner

Tissue-specific DNA-PK-dependent H2AX phosphorylation and gamma-H2AX elimination after X-irradiation in vivo

Differential subcellular localization of DNAdependent protein kinase components Ku and DNA-PKcs during mitosis

Validation of the γH2AX biomarker for genotoxicity assessment: a review

Characterisation of Crandell-Rees Feline Kidney (CRFK) cells as mesenchymal in phenotype

Ionizing radiation-induced cellular senescence in normal, non-transformed cells and the involved DNA damage response: a mini review

Repair of ionizing radiation-induced DNA double-strand breaks by non-homologous endjoining

Radiation therapy for the treatment of tumours in small companion animals

Translational research in radiation-induced DNA damage signaling and repair

Emerging translational opportunities in comparative oncology with companion canine cancers: radiation oncology

Pet animals with cancer help advance human cancer research: similarities help to explore future human treatments

DNA damage foci: Meaning and significance

ATM and DNA-PK function redundantly to phosphorylate H2AX after exposure to ionizing radiation

Production of polyclonal antibody against kidney antigens: a model for studying autoantibody in feline chronic kidney diseases

Profibrotic effects of angiotensin II and transforming growth factor beta on feline kidney epithelial cells

Do DNA double-strand breaks drive aging?

Antibodies against Crandell Rees feline kidney (CRFK) cell line antigens, alpha-enolase, and annexin A2 in vaccinated and CRFK hyperinoculated cats

Common mechanism of infection by lentiviruses

Directed elimination of senescent cells by inhibition of BCL-W and BCL-XL

CONFLICT OF INTEREST. The authors declare no conflict of interest.ACKNOWLEDGMENTS. This work was carried out with the support of National Institutes for Quantum and Radiological Science and Technology, and Department of Regulatory Biology, Faculty of Science, Saitama University.