Cell Proliferation Analysis Research Articles

CircRNA8924-Transfected Bone Marrow Mesenchymal Stem Cells (BMSCs) Affects the Biological Behaviors of Hela Cells

This study investigated the effect of BMSCs transfected with CircRNA8924 on biological behaviors of Hela cells. The transfected BMSCs was then co-cultured with Hela cells and divided into CircRNA8924 mimic group, CircRNA8924 inhibitor group, and CircRNA8924 NC group followed by analysis of cell proliferation, apoptosis, migrated and invaded capacity as well as CirRNA8924 and CBX8 expression. CircRNA8924 mimic group showed highest CircRNA8924 expression followed by NC group and Inhibitor group. CircRNA8924 Inhibitor group presented significantly reduced cell proliferation and cells at S stage, decreased cell migrated and invaded capacity and elevated cell apoptotic activity (P < 0.05) compared to other two groups. In addition, significantly downregulated CircRNA8924 and CBX8 was also found in CircRNA8924 Inhibitor group (P < 0.05). In conclusion, BMSCs transfected with CircRNA8924 could down-regulate CBX8 and CircRNA8924 so as to exert regulatory action on the biological behaviors of Hela cells, indicating that CBX8 might be a therapeutic target for treating cervical cancer.

Effect of Krüppel-Like Factor 7 (KLF7) on High Sugar Induced Retinal Ganglion Cell Biological Activity and Oxidative Stress

This study investigated KLF7’s effect on sugar induced retinal ganglion cells (RGCs) biological activity. The RGCs cells divided into blank group (RA), high sugar group (RB), high sugar+NC group (RC) and high sugar+KLF7 group (RD) (transfected with KLF7 mimic) followed by analysis cell proliferation by MTT, cell apoptosis by flow cytometry and protein expression by western blot and ROS level. RB and RC group showed significantly reduced KLF7 mRNA and protein level compared to RA group (P < 0.05) without different between RB and RC group (P > 0.05). RD group had significantly increased LKF7 and Sirt1 protein expression (F = 113.3, P < 0.0, 01), reduced cell proliferation (P < 0.05) and increased RGCs apoptosis rate (P < 0.05) compared with RB and RC group. After 24 h, RB and RC group presented significantly higher ROS level (P < 0.05) which was reduced in RD group (P < 0.05). In conclusion, KLF7 can change sugar induced retinal ganglion cell biological activity and reduce the oxidative stress level.

MiR-653 Induces Bone Marrow Mesenchymal Stem Cells Proliferation via Activating Epithelial-Mesenchymal Transition in Oral Squamous Cell Carcinoma

This study intends to assess miR-653’s expression in MSCs and OSCC and discuss molecular biological mechanism of changes of EMT in MSCs through activating miR-653 in OSCC. miR-653 expression in MSCs and OSCC was detected. si-miR-653 was transfected into MSCs followed by analysis of cell proliferation by CCK-8 and clone formation assay, cell apoptosis and cycle by FCM, and the changes of transcription factor as ZEB1 and Snail by qRT-PCR. miR-653 expression in OSCC cell was up-regulated significantly from the result of q-RT-PCR detection. The proliferation of MSCs induced by miR-653 was restrained and apoptotic rate was increased after treatment with si-miR-653 along with stagnated cycle of G1/G0 staging cell. The expression of transcription factor of EMT type as ZEB1 and Snail was elevated significantly after intervention using si-miR-653. In conclusion, the proliferation of OSCC could be induced by MSCs through activation with miR-653 which might be through regulation of EMT process.

Morphological and histological changes in the genital ducts of the male Atlantic stingray, Dasyatis sabina, during the seasonal reproductive cycle

Changes inthe morphology and histologyofthe epididymis and seminal vesicle in male Atlantic stingrays (Dasyatis sabina) were examined in relation tothe seasonal reproductive cycle. Observations onthe size and structureofthese organs were accompanied by analysisof cell proliferation in genital duct epithelia using proliferating cell nuclear antigen (PCNA) as a marker for mitotic activity. No signsof reproductive tract growth or histological alteration were apparent duringthe initial stagesof spermatogenesis. However, increased PCNA expression inthe seminal vesicle epithelium was observed during this period, suggesting that this organ begins to undergo preparatory changes at an early stage inthe reproductive cycle. During late spermatogenesis, heightened expressionof PCNA in epithelial cellsofthe epididymis and seminal vesicle was observed in conjunction with dramatic increases in size and semen contentofthese organs. Extensive changes inthe histological architectureofthe genital ducts also were evident at this time, including regressionofthe stroma and an increase in size and secretory activityofthe epithelium. Althoughthe epididymis regressed in size and structure shortly after sperm production was completed,the seminal vesicle retained its appearance and activity forthe durationofthe 7-month copulatory period. Afterwards, immune cell content increased considerably in both ducts, likely reflecting clearanceof residual spermatozoa in preparation forthe subsequent reproductive season.the present study provides a basis for future reports onthe physiological regulationof reproductive tract function in elasmobranchs, and establishes PCNA immunocytochemistry as a novel tool for such investigations.