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Full-Text Articles in Life Sciences

Toxicity Of Cdse Nanoparticles In Caco-2 Cell Cultures, Lin Wang, Dattatri K. Nagesha, Selvapraba Selvarasah, Mehmet R. Dokmeci, Rebecca L. Carrier Jun 2011

Toxicity Of Cdse Nanoparticles In Caco-2 Cell Cultures, Lin Wang, Dattatri K. Nagesha, Selvapraba Selvarasah, Mehmet R. Dokmeci, Rebecca L. Carrier

Dattatri K. Nagesha

BackgroundPotential routes of nanomaterial exposure include inhalation, dermal contact, and ingestion. Toxicology of inhalation of ultra-fine particles has been extensively studied; however, risks of nanomaterial exposure via ingestion are currently almost unknown. Using enterocyte-like Caco-2 cells as a small intestine epithelial model, the possible toxicity of CdSe quantum dot (QD) exposure via ingestion was investigated. Effect of simulated gastric fluid treatment on CdSe QD cytotoxicity was also studied. ResultsCommercially available CdSe QDs, which have a ZnS shell and poly-ethylene glycol (PEG) coating, and in-house prepared surfactant coated CdSe QDs were dosed to Caco-2 cells. Cell viability and attachment were studied …


Toxicity Of Cdse Nanoparticles In Caco-2 Cell Cultures, Lin Wang, Dattatri K. Nagesha, Selvapraba Selvarasah, Mehmet R. Dokmeci, Rebecca L. Carrier May 2011

Toxicity Of Cdse Nanoparticles In Caco-2 Cell Cultures, Lin Wang, Dattatri K. Nagesha, Selvapraba Selvarasah, Mehmet R. Dokmeci, Rebecca L. Carrier

Rebecca L. Carrier

BackgroundPotential routes of nanomaterial exposure include inhalation, dermal contact, and ingestion. Toxicology of inhalation of ultra-fine particles has been extensively studied; however, risks of nanomaterial exposure via ingestion are currently almost unknown. Using enterocyte-like Caco-2 cells as a small intestine epithelial model, the possible toxicity of CdSe quantum dot (QD) exposure via ingestion was investigated. Effect of simulated gastric fluid treatment on CdSe QD cytotoxicity was also studied. ResultsCommercially available CdSe QDs, which have a ZnS shell and poly-ethylene glycol (PEG) coating, and in-house prepared surfactant coated CdSe QDs were dosed to Caco-2 cells. Cell viability and attachment were studied …


Toxicity Of Cdse Nanoparticles In Caco-2 Cell Cultures, Lin Wang, Dattatri Nagesha, Selvapraba Selvarasah, Mehmet Dokmeci, Rebecca Carrier May 2011

Toxicity Of Cdse Nanoparticles In Caco-2 Cell Cultures, Lin Wang, Dattatri Nagesha, Selvapraba Selvarasah, Mehmet Dokmeci, Rebecca Carrier

Mehmet R. Dokmeci

Background
Potential routes of nanomaterial exposure include inhalation, dermal contact, and ingestion. Toxicology of inhalation of ultra-fine particles has been extensively studied; however, risks of nanomaterial exposure via ingestion are currently almost unknown. Using enterocyte-like Caco-2 cells as a small intestine epithelial model, the possible toxicity of CdSe quantum dot (QD) exposure via ingestion was investigated. Effect of simulated gastric fluid treatment on CdSe QD cytotoxicity was also studied.


Results
Commercially available CdSe QDs, which have a ZnS shell and poly-ethylene glycol (PEG) coating, and in-house prepared surfactant coated CdSe QDs were dosed to Caco-2 cells. Cell viability and attachment …


Causes, Extent, And Consequences Of Lead-Pellet Ingestion By Chukars (Alectoris Chukar) In Western Utah: Examining Habitat, Search Images, And Toxicology, R. Justin Bingham May 2011

Causes, Extent, And Consequences Of Lead-Pellet Ingestion By Chukars (Alectoris Chukar) In Western Utah: Examining Habitat, Search Images, And Toxicology, R. Justin Bingham

All Graduate Theses and Dissertations, Spring 1920 to Summer 2023

Lead ingestion adversely affects humans and over 130 species of wildlife. Wild chukars (Alectoris chukar) are documented to ingest lead, but the causes and consequences of this ingestion are poorly understood. The objectives of this research were to 1) examine the influence of habitat use, the hunting season, and seasonal climate on the extent and severity of lead ingestion by chukars in western Utah, 2) assess the effects of habitat use, feeding behaviors, and lead density on the causes of lead-pellet ingestion in captive and wild chukars, and 3) investigate the consequences of lead-pellet ingestion in captive chukars as a …


Response Of Monovalent Cation Transporters To Pro-Apoptotic Protein Kinase C Modulators In Human Lens Epithelial Cells, Michael Anthony Lepera Jan 2011

Response Of Monovalent Cation Transporters To Pro-Apoptotic Protein Kinase C Modulators In Human Lens Epithelial Cells, Michael Anthony Lepera

Browse all Theses and Dissertations

Protein kinase inhibition by staurosporine causes apoptotic volume decrease involving potassium (K) channels in immortalized human B3 lens epithelial cells (LECs). Here, the effect of two pro-apoptotic protein kinase C (PKC) inhibitors [12-O-tetradecanoyl-phorbol-13-acetate (TPA) and chelerythrine (CET)] were studied on membrane K transport in a fetal human LEC line (FHL124) by western blotting, immunofluorescence, ion flux, ATP, apoptosis, and biotinylation assays. Long term TPA exposure (0-6 h) inhibited 75% of Na-K-2Cl cotransport (NKCC). In contrast, short term (0-20 min) exposure to 50 μM CET reduced Na/K pump and NKCC by >90% and >70%, respectively, without retrieval from the membrane into …


Differentiation Of Megakaryocytes/Platelets And Neurons From Human Endometrial Stromal Progenitor Cells, Jinju Wang Jan 2011

Differentiation Of Megakaryocytes/Platelets And Neurons From Human Endometrial Stromal Progenitor Cells, Jinju Wang

Browse all Theses and Dissertations

Human endometrium is a high dynamic tissue that contains stem/progenitor cells. These endometrial stromal progenitor cells (hESCs) have been differentiated into a number of mesodermal lineages. There is limited information on differentiating hESCs into neurons, and no information on differentiating hESCs into megakaryocytes (MKs) and platelets (PLTs). The aim of this work was to investigate the possibility of differentiating hESCs into two distinct lineages: MKs, with subsequent PLT formation, and neurons.

We isolated hESCs from human endometrial tissue and cultured the cells for 4-6 passages. Before each differentiation experiment, the purity of hESCs was confirmed by flow cytometry analysis which …