Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
Mitochondrial DNA B Resour ; 3(2): 972-973, 2018 Oct 30.
Article in English | MEDLINE | ID: mdl-33474384

ABSTRACT

The complete mitochondrial genome of a freshwater planorbid snail, Planorbella duryi (Mollusca, Gastropoda) was recovered from de novo assembly of genomic sequences generated with the Illumina NextSeq500 platform. The P. duryi mitogenome (14,217 base pairs) is AT rich (72.69%) and comprises 13 protein-coding genes, two ribosomal subunit genes, and 22 transfer RNAs. The gene order is identical to that of Biomphalaria glabrata and other snail species in the family Planorbidae. This is the first full characterization of a mitochondrial genome of the genus Planorbella.

2.
Appl Biochem Biotechnol ; 160(3): 751-63, 2010 Mar.
Article in English | MEDLINE | ID: mdl-19172232

ABSTRACT

Health risks associated with inhalation and deposition of biological materials have been a topic of great concern due to highly publicized cases of inhalation anthrax, of new regulations on the release of particulate matter, and to increased concerns on the hazards of indoor air pollution. Here, we present an evaluation of the sensitivity of two immortal cell lines (A549, human lung carcinoma epithelia) and NR8383 (rat alveolar macrophages) to a variety of bacterial-derived inhalation hazards and simulants including etoposide, gliotoxin, streptolysin O, and warfarin. The cell response is evaluated through quantification of changes in mitochondrial succinate dehydrogenase activity, release of lactate dehydrogenase, initiation of apoptosis, and through changes in morphology as determined by visible light microscopy and scanning electron microscopy. These cells display dose-response relations to each toxin, except for triton which has a step change response. The first observable responses of the epithelial cells to these compounds are changes in metabolism for one toxin (warfarin) and alterations in membrane permeability for another (gliotoxin). The other four toxins display a similar time course in response as gauged by changes in metabolism and loss of membrane integrity. Macrophages are more sensitive to most toxins; however, they display a lower level of stability. This information can be used in the design of cell-based sensors responding to these and similar hazards.


Subject(s)
Bacterial Toxins/toxicity , Epithelial Cells/cytology , Epithelial Cells/drug effects , Lung/cytology , Macrophages/cytology , Macrophages/drug effects , Apoptosis/drug effects , Biomimetic Materials/toxicity , Cell Line , Cell Membrane/drug effects , Cell Membrane/metabolism , Epithelial Cells/metabolism , Epithelial Cells/ultrastructure , Humans , Inhalation , Macrophages/metabolism , Macrophages/ultrastructure , Microscopy, Electron, Scanning , Time Factors
SELECTION OF CITATIONS
SEARCH DETAIL
...