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The biological multifunctional therapeutic effect of PFD@NGHP was assessed through a comprehensive evaluation. (A) Establishment schematic of Transwell assay system to evaluate the proliferation inhibition of PFD@NGHP. (B) Cell viability of PSCs determined by Transwell assay system. PFD@NGHP exhibited the most potent inhibitory profile. (C) Cell viability of different cell lines (PANC-1 cells, hPSCs, PANC02 cells, and mPSCs) was assessed via CCK-8 kit after different treatments including combination therapy or monotherapy. (D) Expression levels of collagen I, TGF-β1, α-SMA and α-tubulin in hPSC and mPSC lines treated under different conditions for 48 h, as determined by Western blotting. Con, control. (E) TGF-β1 secretion of hPSC and human cell coculture system (H-Co) under different conditions was evaluated by ELISA. Irradiated (RT+) cells and unirradiated (RT−) cells were both analyzed. (F) TGF-β1 secretion of mPSC and mouse cell coculture system (M-Co) under different conditions was evaluated by ELISA. Irradiated cells and unirradiated cells were both analyzed. (G) FCM analysis of PD-L1-targeting by NGHP in PANC-1 and PAN02 cells. NC, negative control. (H) ADCC assay was used to assess the functional status of αPD-L1 in NGHP. ADCC in PANC-1 and IR-PANC-1 (irradiated PANC-1) cells, mediated by different samples (“mNG” was mPEGS-nanogel), was induced using <t>PBMC.</t> All data are exhibited as the means ± SD ( n = 3), and the inserted asterisks indicate statistically significant differences based on * P < 0.05, ** P < 0.01, and *** P < 0.001.
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The biological multifunctional therapeutic effect of PFD@NGHP was assessed through a comprehensive evaluation. (A) Establishment schematic of Transwell assay system to evaluate the proliferation inhibition of PFD@NGHP. (B) Cell viability of PSCs determined by Transwell assay system. PFD@NGHP exhibited the most potent inhibitory profile. (C) Cell viability of different cell lines (PANC-1 cells, hPSCs, PANC02 cells, and mPSCs) was assessed via CCK-8 kit after different treatments including combination therapy or monotherapy. (D) Expression levels of collagen I, TGF-β1, α-SMA and α-tubulin in hPSC and mPSC lines treated under different conditions for 48 h, as determined by Western blotting. Con, control. (E) TGF-β1 secretion of hPSC and human cell coculture system (H-Co) under different conditions was evaluated by ELISA. Irradiated (RT+) cells and unirradiated (RT−) cells were both analyzed. (F) TGF-β1 secretion of mPSC and mouse cell coculture system (M-Co) under different conditions was evaluated by ELISA. Irradiated cells and unirradiated cells were both analyzed. (G) FCM analysis of PD-L1-targeting by NGHP in PANC-1 and PAN02 cells. NC, negative control. (H) ADCC assay was used to assess the functional status of αPD-L1 in NGHP. ADCC in PANC-1 and IR-PANC-1 (irradiated PANC-1) cells, mediated by different samples (“mNG” was mPEGS-nanogel), was induced using PBMC. All data are exhibited as the means ± SD ( n = 3), and the inserted asterisks indicate statistically significant differences based on * P < 0.05, ** P < 0.01, and *** P < 0.001.

Journal: Biomaterials Research

Article Title: Rescue Radiosensitization of Pancreatic Cancer via PD-L1/TGF-β1 Dual-Blockade Nanotherapy as Evaluated in 3-Dimensional Microtumors

doi: 10.34133/bmr.0335

Figure Lengend Snippet: The biological multifunctional therapeutic effect of PFD@NGHP was assessed through a comprehensive evaluation. (A) Establishment schematic of Transwell assay system to evaluate the proliferation inhibition of PFD@NGHP. (B) Cell viability of PSCs determined by Transwell assay system. PFD@NGHP exhibited the most potent inhibitory profile. (C) Cell viability of different cell lines (PANC-1 cells, hPSCs, PANC02 cells, and mPSCs) was assessed via CCK-8 kit after different treatments including combination therapy or monotherapy. (D) Expression levels of collagen I, TGF-β1, α-SMA and α-tubulin in hPSC and mPSC lines treated under different conditions for 48 h, as determined by Western blotting. Con, control. (E) TGF-β1 secretion of hPSC and human cell coculture system (H-Co) under different conditions was evaluated by ELISA. Irradiated (RT+) cells and unirradiated (RT−) cells were both analyzed. (F) TGF-β1 secretion of mPSC and mouse cell coculture system (M-Co) under different conditions was evaluated by ELISA. Irradiated cells and unirradiated cells were both analyzed. (G) FCM analysis of PD-L1-targeting by NGHP in PANC-1 and PAN02 cells. NC, negative control. (H) ADCC assay was used to assess the functional status of αPD-L1 in NGHP. ADCC in PANC-1 and IR-PANC-1 (irradiated PANC-1) cells, mediated by different samples (“mNG” was mPEGS-nanogel), was induced using PBMC. All data are exhibited as the means ± SD ( n = 3), and the inserted asterisks indicate statistically significant differences based on * P < 0.05, ** P < 0.01, and *** P < 0.001.

Article Snippet: The human peripheral blood mononuclear cells (PBMCs) were purchased from iXCells Biotechnologies (CA, USA).

Techniques: Transwell Assay, Inhibition, CCK-8 Assay, Expressing, Western Blot, Control, Enzyme-linked Immunosorbent Assay, Irradiation, Negative Control, ADCC Assay, Functional Assay