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1.
Toxicol In Vitro ; 16(3): 229-33, 2002 Jun.
Article in English | MEDLINE | ID: mdl-12020595

ABSTRACT

Some protease inhibitors (PI), such as the soybean Bowman-Birk protease inhibitor (SBBI), have been described as anticarcinogenic agents. Although PI are ubiquitous compounds in living organisms, the anticarcinogenic potential of PIs other than SBBI remain poorly explored. We evaluated the antiproliferative effect of a protein fraction from tepary bean (Phaseolus acutifolius) seeds with protease inhibitor activity (TPIF), on normal and on malignant cells. TPIF was obtained after precipitation with ammonium sulfate and gel filtration, and its bioactivity was assayed in vitro on HeLa cells, normal 3T3 fibroblasts and 3T3/v-mos transformed fibroblasts. TPIF showed antiproliferative and cytotoxic effects on 3T3/v-mos transformed fibroblasts in a dose-dependent way. On the contrary, TPIF was only cytostatic for normal 3T3 cells at the highest doses assayed, and had no effect on epithelial HeLa cells proliferation. Sublethal TPIF doses also stimulated cell adhesion of poorly adherent 3T3/v-mos cell line.


Subject(s)
Cell Line, Transformed/drug effects , Cytotoxins/toxicity , Phaseolus , Protease Inhibitors/toxicity , 3T3 Cells , Animals , Cell Adhesion/drug effects , Cell Division/drug effects , Cell Line, Transformed/pathology , Dose-Response Relationship, Drug , Electrophoresis, Polyacrylamide Gel , Fibroblasts/drug effects , Fibroblasts/pathology , HeLa Cells , Humans , Mice , Plant Extracts/chemistry
2.
J Neurosci Res ; 68(1): 46-58, 2002 Apr 01.
Article in English | MEDLINE | ID: mdl-11933048

ABSTRACT

We report the establishment of continuously growing cell lines from spinal cords of normal and trisomy 16 fetal mice. We show that both cell lines, named M4b (derived from a normal animal) and MTh (trisomic) possess neurological markers by immunohistochemistry (neuron specific enolase, synaptophysin, microtubule associated protein-2 [MAP-2], and choline acetyltransferase) and lack glial traits (glial fibrillary acidic protein and S100). MTh cells were shown to overexpress mRNA of Cu/Zn superoxide dismutase, whose gene is present in autosome 16. We also studied intracellular Ca2+ signals ([Ca2+]i) induced by different agonists in Indo-1 loaded cells. Basal [Ca2+]i was significantly higher in MTh cells compared to M4b cells. Glutamate (200 microM) and (1S,3R)-1-aminocyclopentane-1,3-dicarboxylic acid (ACDP) (100 microM) induced rapid, transient increases in [Ca2+]i in M4b and MTh cells, indicating the presence of glutamatergic metabotropic receptors. N-methyl-D-aspartate (NMDA) and kainate, but not alpha-amino-hydroxy-5-methylisoxazole-4-propionic acid (AMPA), produced [Ca2+)]i rises in both cell types. MTh cells exhibited faster time-dependent decay phase kinetics in glutamate-induced responses compared to M4b cells. Nicotine induced a transient increase in [Ca2+]i in M4b and MTh cells, with significantly greater amplitudes in the latter compared to the former. Further, both cell types responded to noradrenaline. Finally, we examined cholinergic function in both cell lines and found no significant differences in the [3H]-choline uptake, but fractional acetylcholine release induced by either K+, glutamate or nicotine was significantly higher in MTh cells. These results show that M4b and MTh cells have neuronal characteristics and the MTh line shows differences which could be related to neuronal pathophysiology in Down's syndrome.


Subject(s)
Cell Line, Transformed , Down Syndrome , Neurons/chemistry , Spinal Cord/cytology , Trisomy , Acetylcholine/metabolism , Animals , Calcium/metabolism , Calcium Signaling , Cell Culture Techniques , Cell Line, Transformed/metabolism , Cell Line, Transformed/pathology , Choline/metabolism , Disease Models, Animal , Down Syndrome/physiopathology , Excitatory Amino Acid Agonists/pharmacology , Immunoblotting , Immunohistochemistry , Mice , Mice, Inbred C57BL , Mice, Mutant Strains , Neurons/pathology , Nicotine/pharmacology , Norepinephrine/pharmacology , Receptors, Glutamate/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Spinal Cord/embryology , Spinal Cord/pathology , Superoxide Dismutase/biosynthesis , Superoxide Dismutase/genetics , Superoxide Dismutase-1
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