Figure 4
Figure 4. Cellular effects of ER stress induced by TM and TG, Hsp90, and proteasome inhibitors. (A) Transcriptional upregulation of EDEM-1, known to accelerate the degradation of misfolded proteins, demonstrated by real-time Taqman PCR. (B) The extent of cytoplasmic inclusions exhibited by U266 in response to treatments (24 hours, IC50 doses: TM, 100 μM; TG, 10 μM; 17-AGG, 5 μM; Bortezomib, 8 nM) was determined using May-Grunwald-Giemsa (MGG) staining and light microscopy (Olympus BH-2 microscope [Olympus, London, United Kingdom] 100×/1.40 oil; images acquired using JVC KY-F1030 digital camera and JVC Scan Rate Converter [Victor, Tokyo, Japan]). (C) Immunoglobulin light chain staining demonstrates a build-up of λ light chain within the inclusions. Representative cell line data on U266 are shown. All experiments were repeated in triplicate.

Cellular effects of ER stress induced by TM and TG, Hsp90, and proteasome inhibitors. (A) Transcriptional upregulation of EDEM-1, known to accelerate the degradation of misfolded proteins, demonstrated by real-time Taqman PCR. (B) The extent of cytoplasmic inclusions exhibited by U266 in response to treatments (24 hours, IC50 doses: TM, 100 μM; TG, 10 μM; 17-AGG, 5 μM; Bortezomib, 8 nM) was determined using May-Grunwald-Giemsa (MGG) staining and light microscopy (Olympus BH-2 microscope [Olympus, London, United Kingdom] 100×/1.40 oil; images acquired using JVC KY-F1030 digital camera and JVC Scan Rate Converter [Victor, Tokyo, Japan]). (C) Immunoglobulin light chain staining demonstrates a build-up of λ light chain within the inclusions. Representative cell line data on U266 are shown. All experiments were repeated in triplicate.

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