Scorpion venom peptide SPVII promotes irradiated cells proliferation and increases the expression of the IL-3 receptor

Background The previous investigation demonstrated the radioprotective efficacy of peptides isolated from the venom of Buthus Martti Karsch. In this study, the effect of isolated scorpion venom peptide II (SVPII) on irradiated M-NFS-60 cells and mouse bone marrow mononuclear cells (BM-MNCs) was observed. The AlamarBlue cell viability assay, a colony-forming unit (CFU) assay, flow cytometry (FCM), immunofluorescence, and Western blotting were used to evaluate cell proliferation, cell cycle progression, and the expression of the IL-3 receptor (IL-3R) protein in non-irradiated and irradiated cells. Results Proliferation of irradiated M-NFS-60 cells was significantly accelerated by SPVII, and this effect was further enhanced by co-application of IL-3. Similarly, SPVII increased the number of BM-MNC CFUs and this proliferative effect was greater in the presence of SVPII plus IL-3. In addition, SPVII significantly altered cell cycle progression; SVPII enhanced the fraction of unirradiated M-NFS-60 cells in S phase and the fraction of irradiated M-NFS-60 cells arrested in G2/M. The expression of IL-3R protein by unirradiated M-NFS-60 cells was enhanced significantly by SVPII, and SVPII-induced IL-3R overexpression was 10-fold greater in irradiated M-NFS-60 cells. Conclusions These results indicated the hematopoietic growth factor (HGF)-like effects of SVPII on irradiated cells, possibly mediated by upregulation of IL-3R.


Background
Irradiation therapy serves as one of the main treatments for malignant carcinoma. Radiotherapy kills cancer cells, but also injures actively proliferating healthy cells. Bone marrow is among the most vulnerable tissues to radiotherapy-induced damage. Irradiation may lead to hematopoietic failure, significantly decreasing the efficacy of cancer treatment and negatively impacting patient quality of life. The recovery of hematopoiesis relies on the proliferation and differentiation of undamaged hematopoietic stem cells (HSCs) under the regulation of a specific group of cytokines. Hence, recombinant cytokine treatment is the traditional therapy for mitigating the inhibitory effect of irradiation on hematopoiesis [1]. The most common drugs used to reverse hematopoietic suppression are colony stimulating factors (CFSs), including granulocyte CSF (G-CSF), granulocyte-macrophage CSF (GM-CSF) [2], and monocyte-macrophage CSF (M-CSF). However, the efficacy of these CSFs is limited and cytokine treatment also causes additional adverse events [3,4].
Agents that confer radiation-resistance have been studied for over 40 years. Thousands of potential agents have been investigated, including sulfur compounds and vitamins [5], plant-derived drugs [6,7] and cytokines [8]. However, most of these agents are unable to satisfy the requirements of effectiveness, low toxicity and specificity. Our previous research indicated that scorpion venom peptides (SVPs) protected against radiation-induced bone marrow injury, accelerated the formation of hematopoietic cell colonies following irradiation, and increased the levels of several cytokines in bone marrow and blood, resulting in enhanced recovery of hematopoiesis in irradiated mice [9][10][11]. Based on the outcomes of our preliminary investigation, the proliferation accelerating effect and mechanisms of SVPs on the cytokine-dependent M-NFS-60 cell line (ATCC: CRL-1838™), un-irradiated or irradiated, and primary mouse bone marrow mononuclear cells (BM-MNCs) were observed.
The proliferation of M-NFS-60 cells depends on both M-CSF and IL-3. Under cytokine treatment, M-NFS-60 cells rapidly proliferate but maintain the characteristics of immature bone marrow cells [12]. Therefore, M-NFS-60 cells are commonly used for studies on hematopoiesis. IL-3 promotes pleuripotent hematopoiesis by stimulating the self-renewal of early pleuripotent stem cells and the proliferation and differentiation of marrow-derived progenitor cells, resulting in the continued production and survival of mature blood cells [13,14]. Previous studies confirmed that IL-3 can protect bone marrow cells against radiationinduced apoptosis and regulate the expression of certain oncogenes such as c-myc. In addition, IL-3 protects bone marrow cells against DNA damaging agents [15]. In this study, M-NFS-60 and BM-MNCs cells were treated with either SVPII alone or in combination with IL-3. SVPII promoted the proliferation of irradiated M-NFS-60 cells and stimulated the colony formation of non-irradiated bone marrow cells. These effects were further increased when SVPII was combined with IL-3. Furthermore, SVPII significantly altered M-NFS-60 cells cycle progression, increasing the fraction of unirradiated cells in S phase and irradiated cells in G2/M. In addition, SVPII upregulated the expression of the IL-3 receptor (IL-3R), especially following irradiation, suggesting that the proliferation accelerating effect of SVPII on irradiated cells depends on activation of IL-3R-mediated signaling pathways.

Effect of SVP on the proliferation of irradiation or nonirradiation M-NFS-60 cells
The proliferation of non-irradiated M-NFS-60 cells was markedly enhanced by treatment with scorpion venom proteins SVPII and SVPIII (1-3 mg/L for 24 or 48 h). Proliferation was greater at 3 mg/L than at 4 mg/L (data not show), so all subsequent experiments were conducted using the optimal concentration range of 1-3 mg/L. The proliferation of irradiated M-NFS-60 cells was accelerated by SVPII and SVPIII (3 mg/L for 48 h) as revealed by the AlamarBlue cell viability assay (P < 0.01; Figure 1). Proliferation was also enhanced by IL-3 alone (10 μg/L for 48 h). The combination of SVP (SVPII or SVPIII at 3 mg/L) plus IL-3 for 48 h exerted the greatest effect on cell proliferation (P < 0.01 vs. control; P < 0.05 vs. SVP alone; Figure 1). Thus, both SVPs and IL-3 promoted the proliferation of irradiated M-NFS-60 cells and the effect of combined SVP + IL-3 treatment was more obvious. As SVPII + IL-3 exerted a larger proliferative effect than SVPIII + IL-3, SVPII was used in all the subsequent experiments.
Effect of SVP on mouse hematopoietic cell CFU count BM-MNCs were isolated from BALB/C mice and used to examine the effect of SVPII on primary hematopoietic cell proliferation and survival. Isolated BM-MNCs were cultured for up to 14 days in methyl cellulose medium with SVPII (1 mg/L or 3 mg/L) or SVPll plus the cytokines IL-3 (10 μg/L) and rhM-CSF (62 μg/L). Treatment with SVPII alone increased the CFU count; the CFU count in 1 mg/L SVPII alone peaked on the 7 th day after administration and then declined (P < 0.05 on day 7 vs. controls), while the CFU count in 3 mg/L SVPII was higher on the 11 th and 14 th day compared to the 7 th day and significantly greater than PBS-treated controls on all measurement days (P < 0.05) (Table 1, Figure 2). The CFU number in cytokine-treated groups peaked on day 7 and remained significantly higher than controls on all subsequent days (P < 0.05). At all measured time points, the CFUs were higher in the 1 mg/L SVPII + cytokines group and the 3 mg/L SVPII + cytokine group compared to all other treatment groups, consistent with the synergistic effect of SPVII plus cytokines observed in M-NFS-60 cells. The CFU count in the 1 mg/L SVPII + cytokines group peaked on the 7 th day (P < 0.05) and then declined, while the CFU count in the 3 mg/L SVPII + cytokines group was higher on the 11 th and 14 th day compared to day 7 and significantly higher than all other groups on day 14 (P < 0.05).  (Table 3).
After irradiation by 60 Coγ-ray, M-NFS-60 cells were incubated in culture medium containing 10% FCS, 15.5 μg/L rhM-CSF (25% of the normal dose), and 3 mg/L SVPII for 48 h and cell cycle progression compared to   unirradiated cells, irradiated cells without SPVII, and irradiated cells treated with 10 μg/L IL-3 (Table 4). After irradiation and 48 h incubation in media with 25% rhM-CSF (15.5 μg/L), 32.21% of M-NFS-60 cells were in S phase and 31.71% were in G2-M phase. For irradiated cells treated with IL-3 for 48 h, the proportion of cells in G2-M phase was significantly higher (65.38%), as were the percentage of apoptotic cells (31.95%). For the irradiated cells treated with SVPII for 48 h, 46.27% were arrested at G2-M phase, significantly higher than in irradiated group (drug-free). However, the percentage of cells in S phase was significantly decreased and the fraction of apoptotic cells was lower than in the IL-3 treatment group.

Effect of SVP on the expression of IL-3R
Effect of SVP on the expression of IL-3R in M-NFS-60 cells Following 48 h SVPII treatment, the expression level of IL-3R in M-NFS-60 cells was detected by FCM and cell immunoflurorescence. Flow cytometry indicated that the expression of IL-3R was upregulated after SVPII treatment and further enahanced by SVPII plus IL-3 ( Figure 3). Immunofluorescence yielded similar results ( Figure 4). The highest fluorescence intensity was observed in the SVPII + IL-3 group, followed by the IL-3 group, SVPII group, and normal controls (lowest), suggesting that the enhancement of M-NFS-60 cell proliferation by SVP may be associated with upregulation of IL-3R.
The growth of M-NFS-60 cells depends on the cytokine M-CSF. As the expression of IL-3R will be induced by M-CSF, IL-3R expression in response to IL-3 or SVPII was measured at normal M-CSF dose (62.5 μg/L) and 25% of the normal M-CSF dose (15.5 μg/L). Western blotting results revealed that SVPII significantly upregulated the expression of IL-3R at both M-CSF doses, while SPVII plus IL-3 exhibited a strengthening effect on IL-3R expression ( Figure 5).

Effect of SVP on the expression of IL-3R in irradiated M-NFS-60 cells
Westerm blot and immunofluorescence results strongly suggested an association between the proliferationpromoting effect of SVPII (and SVPII plus IL-3) and upregulated expression of IL-3R, at least in unirradiated M-NFS-60 cells. In irradiated M-NFS-60 cells, the expression level of IL-3R was also significantly upregulated by 48 h of SVPII treatment and further enhanced by combining SVPII and IL-3 ( Figure 6). Indeed, expression was approximately 10-fold higher than in SVPII-or SVPII + IL-3-treated unirradiated cells, underscoring the possible role of IL-3R overexpression in SVPII-mediated hematopoietic cell proliferation after radiation.

Discussion
Hematopoietic injury is a common and severe complication of radiation treatment for malignant carcinoma, and can lead to anemia, infection, and hemorrhage. Cytokines serve as one of the most effective drugs for the treatment of hematopoietic dysfunction. However, irradiated hematopoietic cells exhibit a decreased proliferative response toward cytokines. Furthermore,    multiple cytokines must be administered to promote the recovery of hematopoiesis, increasing the risk of adverse events and the patients' financial burden [3,4].
Seeking an efficacious irradiation-resistance agent that promotes hematopoiesis with less severe adverse events could greatly improve the therapeutic efficacy of radiation treatment for malignant carcinoma patients.
Preliminary studies indicated that the peptide isolated from Buthus martensii scorpion venom could inhibited the growth of H 22 tumor. When the venom peptide was administered simultaneously with radiation, the inhibiting effect on H 22 was enhanced and radiation injury on H 22 -bearing mice could be antagonized by peptide too [9]. The further study showed that SVPs stimulated the secretion of multiple cytokines (IL-1 α, SCF, IL-6, and GM-CSF) in irradiated mice and increased the count of peripheral leucocytes, bone marrow karyocytes, and the number of CFUs formed by isolated bone marrow cells [10,11]. These results suggested that scorpion venom peptides possess the effect of radiation injury mitigation and tumor suppression. At present study we choose M-NFS-60 cells, which were routinely and widely used for modeling hematopoietic events, as the target cells. Our study demonstrated that the isolated peptides SVPII enhanced the proliferation of M-NFS-60 cells, especially after irradiation. The CFU count of bone marrow cells from BALB/C mice was significantly increased after 7, 11, and 14 days of SVPII treatment. This effect was further enhanced when SVP was combined with IL-3.
The reversal of radiation-induced hematopoietic suppression relies on the survival of hematopoietic stem/ progenitor cells and reactivated proliferation and differentiation. A variety of cytokines are required during the  early-stages of these processes. Alternatively, single and multiple cytokine therapy at advanced-stages of radiationinduced hematopoietic suppression exerted no restorative effect [16]. Hérodin F et al. found that many cytokines, including SCF, FLT-3, TPO, IL-3, and SDF-1 can protect animals from irradiation when administered before the onset of severe damage [16]. Thus, short-and long-term survival after irradiation depends on timely treatment with the appropriate combination of cytokines at optimal concentrations. We observed an enhancing efficacy of SVPII and IL-3 on proliferation in both irradiated and unirradiated M-NFS-60 cells, suggesting that SVPII possesses cytokinelike functions. This combination cytokine therapy not only stimulated cell proliferation, but enabled surviving cells to enter the cell cycle after irradiation. Seven days after irradiation, 35% of cells were arrested in S phase. By contrast, a previous study found that 80% of irradiated cells not treated with IL-3 and stem cell factor failed to enter the cell cycle and a significant fraction became apoptotic [17], indicating that cytokines enhance the recovery of hematopoiesis after irradiation possibly by promoting cell cycle re-entry of HSCs and/or hematopoietic progenitor cells (HPCs). In the current study, the proportion of M-NFS-60 cells at S phase was significantly increased after 24 h of SVPII treatment under serumfree conditions, and the number of cells in S phase was even greater after 96 h treatment. This prolonged SVPII treatment induced more M-NFS-60 cells to enter S phase than IL-3 treatment alone.
Cell cycle arrest and apoptosis are the major mechanisms of radiation-induced bone marrow damage. Damage to DNA activates cell cycle checkpoint proteins and cell cycle arrest at G1 or G2. BAF3 cells resisted X-ray-and cytotoxin-induced injury when the culture media was supplemented with IL-3. Treatment with IL-3 exerted no apparent effect on early-stage DNA damage and repair, but played an essential role in preventing the acceleration of DNA fragmentation at the G2 phase block point [15]. In addition, IL-3 can accelerate G2/M phase arrest and prevent apoptosis of mouse hematopoietic progenitor 32D and human UT7 cell lines in response to etoposide, a type II topoisomerase inhibitor [18]. We found that the proportion of IL-3-treated M-NFS-60 cells arrested at G2/M phase was 65.38%, significantly higher than the 31.71% measured in the control group after irradiation, while the percentage of apoptotic cells (31.95%) was higher than in the control group (15.81%). Gottlieb E et al. [19] observed that IL-3 prevented the apoptosis of DA-1 lymphoma cells at a low irradiation dose. However, p53-dependent DA-1 cell apoptosis occurred at a higher radiation dose even in the presence of IL-3. In our investigation, the relatively high radiation dose used may have overcome the effect of IL-3 so that apoptosis still occurred. However, the number of apoptotic M-NFS-60 cells after SVPII treatment was not significantly different from the irradiated control group. In addition, SVPII had a regulatory effect on cell cycle progression similar to IL-3, significantly increasing the proportion of cells at G2-M phase (to 46.27%) and decreasing the number of cells at S phase. Thus, SVPII has advantages over IL-3 for protecting M-NFS-60 cells in response to a relatively high radiation dose. SVP II may prevent DNA fragmentation and apoptosis at G2 checkpoints after irradiation, although additional studies are necessary to test this possibility.
SVPII promoted the proliferation of IL-3-dependent M-NFS-60 cells, while the combined application of SVPII and IL-3 strengthened the proliferation-promoting effect of either agent alone, suggesting that activation of IL-3R pathways may have contributed to the enhanced proliferation of M-NFS-60 cells. Whether the effects of SVPII and IL-3 were functioned via IL-3Rs was studied by measuring IL-3R expression in M-NFS-60 cells. Both FCM and immunofluorescence results indicated that the expression level of IL-3R was upregulated in M-NFS-60 cells after SVPII treatment. A greater increase in IL-3R expression was measured when M-NFS-60 cells were treated with both SVPII and IL-3, and this enhanced expression was observed under both normal M-CSF and low (25%) M-CSF concentrations. Western blotting also indicated that SVPII significantly upregulated the expression of IL-3R, and exhibited a strengthening effect with IL-3, indicating that the proliferation-enhancing effect of SVPII on M-NFS-60 cells is likely due to IL-3R upregulation. The mutated fibroblast cytokine receptor F36VFGFR1 facilitated the expansion of HSCs in vivo and in vitro, while F36VMpl, a mutant thromboietin receptor, promoted the recovery of myeloid hematopoiesis after irradiation. Other receptors serve as novel regulators of hematopoiesis [20]. Monzen S et al. [21] recently reported that the cytokine receptor genes KIT and IL-3R, as well as genes related to early hematopoiesis and oxidation stress, were all upregulated 7 days after irradiation. Streeter PR et al. [22] indicated that the activation of Flt-3 and G-CSF receptors protected HSCs/HPCs from radiation damage. These studies reveal that cytokine receptors play a vital role in regulating and promoting hematopoiesis after irradiation. The current study demonstrated that IL-3R expression in irradiated M-NFS-60 cells was significantly upregulated 48 h after SVPII treatment. This upregulation was further strengthened by addition of IL-3, indicating that the proliferation promoting effect of SVPII on irradiated cells is closely correlated with upregulation of IL-3R. Hence, IL-3R is a potential therapeutic target for maintaining hematopoietic function following irradiation.

Conclusion
Radiotherapy for cancer patient may lead to hematopoietic failure. Recombinant cytokine treatment is the traditional therapy for mitigating the inhibitory effect of irradiation on hematopoiesis, but cytokine treatment also causes additional adverse events. Thousands of potential agents that confer radiation-resistance have been investigated. The previous investigation demonstrated the radioprotective efficacy and tumor-inhibiting effect of peptides isolated from the scorpion venom of Buthus Martti Karsch. In this paper, we have demonstrated that the proliferation of irradiated M-NFS-60 cells was significantly accelerated by scorpion venom peptide II (SPVII) and induced 10-fold greater overexpression of IL-3R in irradiated M-NFS-60 cells than unirradiated cells. All these effects were further enhanced by co-application of IL-3. Similarly, SPVII increased the number of BM-MNC CFUs and this proliferative effect was greater in the presence of SVPII plus IL-3. SPVII can also alter the cell cycle fractions of M-NFS-60 cells (unirradiated and irradiated). The significance of these results is that SVPII possesses the hematopoietic growth factor (HGF)like effects on irradiated cells and the effect possibly mediated by upregulation of IL-3R. The cytokines similar functions of SVPII and its mechanisms deserve further study.

Agents and materials
The peptides SVPII and SVPIII (used only in AlamarBlue™ assay) were isolated from the venom of Buthus Martti Karsch as described [11]. Recombinant human macrophage colony stimulating factor (rhM-CSF) and recombinant mouse (rm) IL-3 were purchased from PeproTech Co. AlamarBlue™ was purchased from AbD Serotec (Great Britain), and membrane protein isolation kits were from Bio-Rad. An IL-3R antibody was purchased from Abcam Co. Methyl cellulose for CFU assay was from Sigma-Aldrich Co.

Experimental procedures M-NFS-60 cell culture and treatment groups
The M-NFS-60 cell line was cultured in PRMI 1640 culture media supplemented with 10% fetal calf serum (FCS), 100 U/ml penicillin, 100 U/ml streptomycin, 5.958 g/L HEPES, and 62 μg/L rhM-CSF. Cells were maintained at 37°C under a 5% CO 2 atmosphere. The media was changed every other day. Cells were used for experiments in the exponential growth phase. Unirradiated or 60 Coγ-irradiated M-NFS-60 cells were treated with PBS (control), SVPII or SVPIII alone, IL-3 alone, or SVP plus IL-3 for various durations.
Special cell culture methods M-NFS-60 cells were cultured in serum-free media supplemented with 62 μg/L rhM-CSF for 24 h (serum-free) or treated with 3 mg/L SVP II (SVP II) or 10 μg/L IL-3 (IL-3). The control cells were cultured 24 h in normal medium (24 h control). After 24 h, the cell cycle was analyzed by FCM. After cultured in serum-free media plus rhM-CSF for 24 h, the cells were cultured in normal midium (mentioned above) for an additional 72 h (serum-free) or treated with SVPII 3 mg/L or IL-3 10 μg/L in the same media. The control cells were cultured 96 h in normal medium (96 h control). After 96 h, the cell cycle was analyzed by FCM. Serum-free medium will lessen the influence factors on the cell cycle progression.
After irradiation by 60 Coγ-ray M-NFS-60 cells were cultured in PRMI 1640 culture media supplemented with 10% FCS, 100 U/ml penicillin, 100 U/ml streptomycin, 5.958 g/L HEPES, and 15.5 μg/L rhM-CSF (25% of the normal M-CSF dose) for 48 h (irradiated control) or treated with 3 mg/L SVPII or 10 μg/L IL-3 for 48 h. Unirradiated cells were cultured 48 h in the same medium were served as control. After 48 h, the cell cycle was analyzed by FCM.

Cell irradiation
M-NFS-60 cells were irradiated by 60 Coγ-ray at 5 Gy using a Gammacell 3000 Elan installation (Nordion Intern. Inc., Canada). Proliferation and cell cycle progression were then analyzed as described below.

Preparation of mouse BM-MNCs
All animal experiments in this study were approved by the Institutional Animal Care and Use Committee of Guangzhou Medical University. The BALB/C mice were euthanized with CO 2 and the femoral bones removed. The femoral bone cavity was washed with low-sugar DMEM medium to harvest bone marrow cells. The cells in DMEM were then slowly added onto the surface of a lymph cell isolation solution and centrifuged at 2000 rpm for 20 min. The annular white layer consisting of monocytes was collected, washed three times in PBS, and resuspended in DMEM at the optimal concentration for each experiment.

AlamarBlue™ cell viability assay
The AlamarBlue assay was used to measure the effect of SVP on the proliferation of non-irradiated and irradiated M-NFS-60 cells cultured in suspension. After irradiation or sham treatment, M-NFS-60 cells were washed three times in PRMI 1640 culture media, and the live cells counted using Trypan Blue vital staining. The cell concentration was adjusted to 5 × 10 4 cells/mL using PRMI 1640 culture media containing 10% FCS and 62 μg/L rhM-CSF, and aliquoted at 80 μL/well in 96-well plates. After 24 h incubation at 37°C, 10 μL PBS (control), SVP (1, 3, or 4 mg/L), IL-3 (10 μg/L), or SVP + IL-3 was added to each well. Each treatment was performed in triplicate in the same 96-well plate. Following control or drug treatment, 10 μL AlamarBlue™ was added to each well and plates incubated at 37°C for 48 h. Optical density (OD) values were measured and the cell proliferation rate calculated.

Colony forming unit (CFU) assay
A methyl cellulose half-solid colony formation method was adopted to measure the number of bone marrow mononuclear cell CFUs under different treatment conditions. Treated BM-MNCs (1 × 10 6 cells/mL) were added into methyl cellulose half-solid medium composed of DMEM, 0.8% methyl cellulose, 30% FCS, 2 mmol/L L-glutamine, and the recombinant cytokines (10 μg/L IL-3 and 62 μg/L rhM-CSF). The CFU number was counted under a microscope after 7, 11, and 14 days of incubation at 37°C in a 5% CO 2 atmosphere. A mass consisting of more than 50 cells was defined as 1 CFU.

Analysis of the cell cycle using FCM
The M-NFS-60 cells (non-irradiated or irradiated) were treated as described. A 0.5 mL cell suspension (1 − 5 × 10 6 / mL) from each treatment group was combined with 2 ml of cooled 70% ethanol and kept overnight at 4°C, centrifuged at 1000 rpm/min, washed in PBS, and incubated in the dark room at 4°C for 30 min with 50 μL RNAse and 450 μL propidium iodide (PI) staining solution. The proportion of cells in each phase of the cell cycle was then determined by PI staining intensity using FACScalibur flow cytometer (Becton Dickinson).

Detection of IL-3R expression
Cell immunofluorescence Cultured M-NFS-60 cells on glass slides were washed twice in PBS, fixed in −20°C pre-cooled 100% methanol for 5 min, dried, and then blocked in 5% BSA solution for 1 h at room temperature or overnight in BSA at 4°C. The blocking solution was removed and anti-IL-3R antibody (Abcam, USA) (1:200) added for 1 h at 37°C or overnight at 4°C. After washing in PBS, an FITC-labeled secondary antibody (F-0382; Sigma) was applied at 1:500 in PBS. Slides were then washed in PBS and sealed in glycerol. The expression of IL-3R was detected by immunofluorescence under a laser scanning confocal microscope (Leica DM1 4000B).
FCM analysis of IL-3R expression Cells were treated as described, harvested, and the concentration of M-NFS-60 cells adjusted to between 5 × 10 6 and 1 × 10 7 cells/mL in PRMI 1640 culture medium. To this cell suspension were added a monoclonal antibody (5-50 μL) and 50 μL inactivated rabbit serum. Cell suspensions were incubated at 4°C for 30 min, washed in PBS, and centrifuged. The supernatants were removed, and the pellets treated with 50 μL of a FITC-conjugated goat anti-mouse antibody, shaken at 4°C for 30 min, washed twice in PBS, centrifuged, and fixed as described in section 3.7.1.
Western blotting Membrane proteins from the different treatment groups were extracted using a Bio-Rad membrane protein extract kit. Total protein concentrations were measured by the Lowry assay and extracts run on 12% SDS-PAGE gels. Separated proteins were electrotransferred to polyvinyl membranes. Membranes were probed with an IL-3R antibody and visualized using chemiluminescence.