6 research outputs found
Cytoskeleton and major extracellular matrix proteins were analyzed by immunofluorescence.
<p>Actin was observed in DPSC (A), DPSC with BD (B) and in DPSC with BR (C); vimentin and tubulin (D, E and F); and type 1 collagen and fibronectin (G, H and I). The observed decrease in type 1 collagen, when DPSC were in contact with biomaterials, was confirmed using RT-qPCR (5J), whereas protein secretion was not modified by the experimental conditions (Fig 5K). Scale Bar: 100μm.</p
Ameloblastin and amelogenin mRNA expression in murine tissues.
<p>Tissues were dissected from 15 week old WT mice (n = 6 with n = 3 females and n = 3 males) and subjected to RT-PCR (see Materials and methods). Resulting products were resolved on a 2% agarose gel. AMBN positive tissues show one amplicon band at 287 bp and AMELX positive tissues show at least one of the three amplicon bands at 415 bp, 373 bp and 303 bp corresponding to transcript variants encoding different isoforms of AMELX described in the literature; at 415 bp (M217 <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0099626#pone.0099626-Bartlett2" target="_blank">[67]</a>–M194 <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0099626#pone.0099626-Simmer1" target="_blank">[68]</a>), 373 bp (M203 <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0099626#pone.0099626-Li2" target="_blank">[69]</a>–M180 <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0099626#pone.0099626-Lau1" target="_blank">[70]</a>) and 303 bp (M179 <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0099626#pone.0099626-Li2" target="_blank">[69]</a>–M156 <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0099626#pone.0099626-Lau1" target="_blank">[70]</a>). +, PCR products were repeatedly obtained; +/−, not all samples were positive; -, no PCR products were visible. The overall high signal in mRNA levels (++) in mandibular mineralized tissues led to perform additional RT-qPCR analyses.</p
Western blot of AMBN and AMELX in 15 week old WT mice.
<p>Proteins were extracted from dental epithelial cells (EP) (positive control), alveolar bone (AB), basal bone (BB) under dissociative and non-dissociative conditions. Proteins were loaded at 10 µg per lane and blots probed with anti-AMBN and anti-AMELX antibodies. <b>A.</b> Anti-AMBN probing of dissociative extracts show cross reactive species with molecular weights ranging from 20–67 kDa for AMBN (the 67 kDa band corresponds to nascent amelobastin). 67 kDa AMBN is present at similar relative amounts in the EP and AB extracts but far less readily detectable in BB. <b>B.</b> A similar situation exists for non-dissociative extracts. <b>C.</b> Anti-AMELX probing of dissociative extracts show cross reactive species at 26 kDa and below in EP samples (higher molecular weight staining may be due to AMELX aggregation). Feint cross reactivity at ∼25 kDa is visible in AB samples with even less been detected in BB; the relative amount of AMELX present in bone samples is far less than that seen in EP samples. <b>D.</b> A similar situation exists for non-dissociative extracts; AMELX is detectable in AB but it is present in the extract in much lower amounts compared to EP extracts.</p
AMBN and AMELX protein expression in 1 week old WT mice.
<p><b>A.</b> AMBN protein (red signal) is strongly expressed in enamel (En) and in dental follicle (DF) and is detected in cells lining alveolar bone (white arrows). <b>B.</b> On serial sections, AMELX protein (green signal) shows similar localization pattern with expression in enamel, dental follicle and bone-lining cells (white arrows). In addition, a diffuse AMELX signal is also detected in periosteum (Po) and bone (Bo) (in particular in matrix of trabebular spaces (white asterisks)). No protein expression is detected in striated muscle (Myo), a negative control tissue. <b>C.</b> Higher magnification of AMELX protein expression shows AMELX-positive osteoblastic cells lining bone trabeculae (red arrows) (<b>Blue box</b>), strong expression in dental follicle area (<b>Yellow box</b>). Higher magnification shows no signal in striated muscle (<b>Orange box</b>). Ambl  =  ameloblast, Bo  =  bone, De  =  dentin, DF  =  dental follicle, En  =  enamel, Myo  =  striated muscle and Po  =  periosteum.</p
AMELX mRNA and protein distribution in mandible from 8 week old WT and AMELX KO mice.
<p><b>A-B. </b><i>In situ</i> hybridization was performed using AMELX oligonucleotidic probes. <b>B.</b> WT mouse shows strong AMELX mRNA level in ameloblasts (Ambl) and odontoblasts (Odb). AMELX mRNA is also detected in bone-lining cells (red arrows) and, with an apparent lower level, in dental follicle (DF) area. <b>C–D.</b> Immunohistodetection was performed using anti-AMELX antibody. <b>D.</b> AMELX protein expression in WT mouse was detected in ameloblasts, odontoblasts and bone-lining cells (red arrows). Strong and diffuse protein signal was also observed in dental follicle. <b>B–D.</b> No AMELX RNA and protein signal is detected in striated muscle (Myo), a negative control tissue (see <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0099626#pone-0099626-t001" target="_blank">Table 1</a>). <b>A–C.</b> Neither AMELX mRNA nor protein expression is detected in AMELX KO mice.</p