Latent mermbrane protein 1(LMP1)is known as an oncoprotein in nasopharyngeal carcinoma(NPC)cells,which is considered to have a strong association with growth,invasion and metastasis of NPC cells through lipid rafts.Me...Latent mermbrane protein 1(LMP1)is known as an oncoprotein in nasopharyngeal carcinoma(NPC)cells,which is considered to have a strong association with growth,invasion and metastasis of NPC cells through lipid rafts.Met hy-A-cyclodextrin(M3CD)can disrupt lipid rafts through cholesterol depletion.In this study,we revealed that MICD induced apoptosis in two kinds of NPC cells including CNE1 cells,a LMP1 negative nasopharyngeal squamous carcinoma cell line,and CNE1-LMP1 cells,a LMP1-positive nasopharyngeal squamous carcinoma cell line.Furthermore,the impact of MBCD on LMP1 was investigated by fuorescence resonance energy transfer(FRET)method in NPC cells.Synchronized tempo spatial and spectral detection of LMP1/LMP1 interaction were performed using fluorescence microscope and spectrograph.FRET efficiency indicated that LMP1/LMP1 interaction gradully enhanced after M9CD treatment.MTT assays showed that M8CD caused strong cytotoxicity in CNE1 cells,but cauused relatively weaker cytotoxicity in CNE1-LMP1 cells,which indicated that LMP1 may regulate sensitivity of NPC cells to MBCD.Then,detection of cleaved caspase-3 in two kinds of NPC cells indicated that LMP1 may inhibit activation of caspase 3.These results strongly suggested that MBCD can induce apoptosis of NPC cells,but enhancing of LMP1/LMP1 interaction may likely resist apoptosis through inhibiting cleavage of caspase-3.展开更多
Glycat ed hemoglobin(HbAlc)has been increasingly accepted as the gold standard for diabetesmonit oring.In this study,Raman spect roso was tentatively emplo yed for human hemoglobin(b)bioc hemical analysis aimed at de ...Glycat ed hemoglobin(HbAlc)has been increasingly accepted as the gold standard for diabetesmonit oring.In this study,Raman spect roso was tentatively emplo yed for human hemoglobin(b)bioc hemical analysis aimed at de veloping a a simple blood test for diabetes monitoring.Ramanspectroscopy measurementsperformed oWereglobimples of patients(n=39)withconfirmed diabetes and healthyvolulhetentatiassignments of the measuredRaman bands were perfortwogegroups.Meanwhile,principal componentaminant analysis(LDA)wereemployed to develop effective weell1ormal controls andpatients with diabetes.Asat wo groups demonstrated twodistinct clust ers with a sensitivity and specificity d 73%,respectively.Then the effectiveness of the diagnostic algorithm based onechnique was confirmed by receiveroperating characteristic(ROC)curve.The area under the ROC curve was 0.92,indicating a good diagnostic result.In summary,our preliminary results demonstrate that proposing Raman spectroscopy can provide a significant potential for the noninvasive detection of diabetes.展开更多
基金supported by the National Key Basic Research Program of China(No.2015CB352006)the National Natural Science Foundation of China(Nos.61335011,61775037 and 61475036)+2 种基金Program for Changjiang Scholars and Innovative Research Team in University(No.IRT 15R10)Natural Science Foundation of Fujian Province of China(Nos.2019J01270 and 2017J01844)the High level Joint Research and Construction Program of Fujian Provincial Hospital,and Special Funds of the Central Government Guiding Local Science and Technology Development(2017L3009),China.
文摘Latent mermbrane protein 1(LMP1)is known as an oncoprotein in nasopharyngeal carcinoma(NPC)cells,which is considered to have a strong association with growth,invasion and metastasis of NPC cells through lipid rafts.Met hy-A-cyclodextrin(M3CD)can disrupt lipid rafts through cholesterol depletion.In this study,we revealed that MICD induced apoptosis in two kinds of NPC cells including CNE1 cells,a LMP1 negative nasopharyngeal squamous carcinoma cell line,and CNE1-LMP1 cells,a LMP1-positive nasopharyngeal squamous carcinoma cell line.Furthermore,the impact of MBCD on LMP1 was investigated by fuorescence resonance energy transfer(FRET)method in NPC cells.Synchronized tempo spatial and spectral detection of LMP1/LMP1 interaction were performed using fluorescence microscope and spectrograph.FRET efficiency indicated that LMP1/LMP1 interaction gradully enhanced after M9CD treatment.MTT assays showed that M8CD caused strong cytotoxicity in CNE1 cells,but cauused relatively weaker cytotoxicity in CNE1-LMP1 cells,which indicated that LMP1 may regulate sensitivity of NPC cells to MBCD.Then,detection of cleaved caspase-3 in two kinds of NPC cells indicated that LMP1 may inhibit activation of caspase 3.These results strongly suggested that MBCD can induce apoptosis of NPC cells,but enhancing of LMP1/LMP1 interaction may likely resist apoptosis through inhibiting cleavage of caspase-3.
基金supported by the National NaturalScience Foundation of China(Nos.11274065,61210016,61308113,61178090 and 81101110)theScience and Technology Project of Fujian Province(No.2012.J01254 and 2013J01225)Program for ChangjiangScholars and Innovative ResearchTeam in University(No.IR T1115).
文摘Glycat ed hemoglobin(HbAlc)has been increasingly accepted as the gold standard for diabetesmonit oring.In this study,Raman spect roso was tentatively emplo yed for human hemoglobin(b)bioc hemical analysis aimed at de veloping a a simple blood test for diabetes monitoring.Ramanspectroscopy measurementsperformed oWereglobimples of patients(n=39)withconfirmed diabetes and healthyvolulhetentatiassignments of the measuredRaman bands were perfortwogegroups.Meanwhile,principal componentaminant analysis(LDA)wereemployed to develop effective weell1ormal controls andpatients with diabetes.Asat wo groups demonstrated twodistinct clust ers with a sensitivity and specificity d 73%,respectively.Then the effectiveness of the diagnostic algorithm based onechnique was confirmed by receiveroperating characteristic(ROC)curve.The area under the ROC curve was 0.92,indicating a good diagnostic result.In summary,our preliminary results demonstrate that proposing Raman spectroscopy can provide a significant potential for the noninvasive detection of diabetes.