Construction of a cDNA library for miniature pig mandibular deciduous molars
- Tieli Song†1, 2,
- Tingting Wu†1,
- Fulan Wei1,
- Ang Li1,
- Fu Wang1,
- Yilin Xie1,
- Dayong Liu1,
- Zhipeng Fan1,
- Xuejiu Wang1,
- Shan Cheng3,
- Chunmei Zhang1,
- Junqi He3 and
- Songlin Wang1, 3Email author
© Song et al.; licensee BioMed Central Ltd. 2014
Received: 20 August 2013
Accepted: 9 April 2014
Published: 21 April 2014
The miniature pig provides an excellent experimental model for tooth morphogenesis because its diphyodont and heterodont dentition resembles that of humans. However, little information is available on the process of tooth development or the exact molecular mechanisms controlling tooth development in miniature pigs or humans. Thus, the analysis of gene expression related to each stage of tooth development is very important.
In our study, after serial sections were made, the development of the crown of the miniature pigs’ mandibular deciduous molar could be divided into five main phases: dental lamina stage (E33-E35), bud stage (E35-E40), cap stage (E40-E50), early bell stage (E50-E60), and late bell stage (E60-E65). Total RNA was isolated from the tooth germ of miniature pig embryos at E35, E45, E50, and E60, and a cDNA library was constructed. Then, we identified cDNA sequences on a large scale screen for cDNA profiles in the developing mandibular deciduous molars (E35, E45, E50, and E60) of miniature pigs using Illumina Solexa deep sequencing. Microarray assay was used to detect the expression of genes. Lastly, through Unigene sequence analysis and cDNA expression pattern analysis at E45 and E60, we found that 12 up-regulated and 15 down-regulated genes during the four periods are highly conserved genes homologous with known Homo sapiens genes. Furthermore, there were 6 down-regulated and 2 up-regulated genes in the miniature pig that were highly homologous to Homo sapiens genes compared with those in the mouse.
Our results not only identify the specific transcriptome and cDNA profile in developing mandibular deciduous molars of the miniature pig, but also provide useful information for investigating the molecular mechanism of tooth development in the miniature pig.
KeywordsTooth Development Histology Unigene Sequence Miniature pig
The pig is a large animal species suitable not only for meat production, but also as a model organism for comparative genomics and biomedical studies [1–6]. Due to the similarity of the dental and jaw bone system between human and pigs [7–9], using swine in dental biomedical research has increased in recent years, including research into dental implants, irradiation damage to parotid glands, bio-root regeneration, osteoradionecrosis, and bisphosphonate-related osteonecrosis, etc. [10–16].
The mouse is the most widely used animal model for studying tooth development. Almost all known molecular mechanisms of tooth formation and mineralization are derived indirectly or directly from studies of murine models [17–19]. However, mouse teeth are different from those of humans in both number and morphology, with only one dentition present throughout the mouse life cycle and a complete absence of canines and premolars . Miniature pigs have both deciduous and permanent dentition, and all tooth types found in humans are present in pigs. However, detailed descriptive information concerning tooth development in the pig is lacking. Recently, our group has been dedicated to investigating the complicated mechanism of tooth development in miniature pigs, including the mRNA expression profiles of developing deciduous molar tooth , and the timing and sequencing of tooth replacement . Other groups also reported that early morphogenesis of heterodont dentition can be divided into four significant stages in miniature pigs . The purpose of the present study was to identify and classify the early stages of odontogenesis in miniature pig’s deciduous molar teeth, focusing on the differential expression of cDNAs during typical periods of tooth development. We also compared the genes from the E45 to E60 time course during tooth development with those of known Homo sapiens genes, and aimed to obtain basic information about their development for further molecular studies. We found that 12 up-regulated and 15 down-regulated genes may be involved in the miniature pig’s tooth development. We also found there were 6 down-regulated and 2 up-regulated genes with high homology to those in Homo sapiens, and compared these with those in mouse.
Pregnant Wuzhishan miniature pigs were obtained from the Institute of Animal Science of the Chinese Agriculture University. Experiments were performed according to the Regulations for the Administration of Affairs Concerning Experimental Animals (Ministry of Science and Technology, China, revised in June 2004), and approved by the Animal Care and Use Committees of Capital Medical University, Beijing, China under permit No. CMU-B20100106. Animals were allowed access to food and water ad libitum under normal conditions and humanely sacrificed as necessary to ameliorate suffering. In brief, pregnant sows were anesthetized with a combination of 6 mg/kg ketamine chloride and 0.6 mg/kg xylazine, and pregnancy and the fetal state roughly determined by B-mode ultrasonography. After removing the fetuses by cesarean section, the pregnant sows were sacrificed by over-anesthetization.
Preparation of tissues and histological staining
Developing miniature pig embryos were obtained by hysterectomy at embryonic days 30 (E30), E35, E40, E45, E50, E55, E60, and E65 according to the developmental progression of deciduous dentition in pigs . After surgically removing the fetuses, germ tissue samples from deciduous molar teeth were removed from the mandibles under a microscope. The first mandibular molar could be obtained from E30. The second mandibular molar could be obtained from E35. The third mandibular molar could be obtained from E45. So the first deciduous mandibular molars were used in all studies. The samples were immediately frozen in liquid nitrogen and stored separately at -80°C until used for analysis. At least five miniature pig embryos were used for each evaluation. Specimens for the histological study were chosen by random selection from each specific age group litter. Embryo mandibles were separated and preserved in 4% paraformaldehyde. Mandible specimens from E30 were placed in EDTA bone decalcifying agent. Serial sections were made of the mandibular deciduous molar region. The tissues were mounted and stained with hematoxylin and eosin.
RNA sample preparation and cDNA library establishment
Mandibular deciduous molar germs from E35, E45, E50, and E60 miniature pig embryos were excised and total RNA was extracted with an RNA purification kit (QIAGEN, Germany). RNA was then mixed in equal amounts from four different developmental time points. Oligo dT cellulose (MicroFast Track, Invitrogen, CA) was used as a template to synthesize first-strand cDNA. The cDNA library was constructed using the SMART cDNA Library Construction Kit (Clontech, CA). The obtained double-stranded (ds)-cDNA was purified using the QIAquick PCR Purification Kit (QIAGEN, Germany), then normalized with the DSN (duplex-specific nuclease) using the Trimmer-Direct Kit (Evrogen, Moscow, Russia). The normalized cDNAs were digested with Sfi I restriction enzyme, size fractionated (1–3 kb), directionally ligated into pDNR-LIB, and transformed into E. coli DH10B by electroporation. The cDNA library was plated on LB plates with X-gal, isopropyl-D-thiogalactopyranoside, and ampicillin. Thirty white colonies were randomly selected for identification of cDNA inserts in the recombinants to estimate the recombination efficiency. Exact same samples were used for both microarray and qRT-PCR.
Microarray targets were prepared from each stage. RNA labelling, hybridization and scanning were conducted by a commercial Affymetrix array service (Institut de Recerca Hospital Universitari Vall d’Hebron, Barcelona, Spain). Reverse transcription of RNA and synthesis of biotin-labelled cRNA with one round of amplification were carried out following the standard Affymetrix one-cycle protocol according to the manufacturer's instructions. Samples were hybridized to the Affymetrix 24 K Genechip® Porcine Genome Array (Affymetrix, Santa Clara, CA, USA). Data analysis was performed with Bioconductor implemented in R 2.6.0 (http://cran.r-project.org/).
Quantitative real-time RT-PCR
Total RNA reversely transcribed into cDNA using the PrimeScriptTM PT Reagent Kit (TaKaRa, Dalian, China). Amplifications of target genes were performed by real-time quantitative PCR (qPCR) using the cDNA as template, the specific primers and the SYBR® PrimeScript® RT–PCR Kit (Takara) on an ABI PRISM 7900 Real Time PCR System (Applied Biosystems, Carlsbad, USA). PCR amplifications were performed in duplicate at 95°C for 15 sec, and subjected to 40 cycles of 95°C for 5 sec 60°C for 30 sec, and 95°C for 15 sec 60°C for 15 sec 95°C for 15 sec. The primers used are shown in Additional file 1. The relative levels of target genes expression to the control of E45 were quantified. The relative levels of target gene mRNA transcripts to control β-actin were determined by 2-ΔΔCt.
cDNA library sequencing, data processing, sequence analysis
After cDNA library identification, large-scale plasmid extraction and sequencing were performed for generation of expressed sequence tags (ESTs). High-quality ESTs were assembled into unigenes by phrap_0.990329 software. The unigene sequences were performed with E-values of less than 10-5 on the GenBank database according to the BLAST Search program (ftp://ftp.ncbi.nih.gov/blast/db/FASTA/). The unigenes were compared with annotations through the Gene Ontology Consortium using Interpro2GO. All ESTs were sequenced and analyzed at a commercial facility (BGI LifeTech Co. Ltd, Beijing, China). If the unigene sequence was more than 100 bp and its homology greater than 90% with a known functional pig gene, this gene was annotated in the pig genes. Then, if the sequence had high homology to a known gene in other species (E-values < 10-5), it was assumed that the gene is an orthologue of the comparator gene.
Data of qRT-PCR are expressed as mean ± SEM. Data were analyzed by one-way analysis of variance. Multiple comparison between the groups was performed by using Bonferroni post-tests method. A p value of less than 0.05 was considered statistically significant. Statistical analysis was carried out using StatView 5.0 software (SAS Institute, Cary, NC) and GraphPad Prism 4.0 software.
Development stages and histological characterization of miniature pig mandibular deciduous molars
E30: In the E30 embryonic mandible, the oral epithelium thickened and extended to form the dental lamina (Figure 1C, G). E35: E35 samples showed hyperplasia of the lamina epithelium cells to form the primary enamel organ, meaning that the typical bud stage was observed (Figure 1D, H). The mesenchymal cells surrounding the bud clearly gathered. The placode was identified between the epithelium and the mesenchyme. E40: In the E40 mandibular region, the molar remained in the bud stage, but minor changes were seen at this time (Figure 1E, I). The peripheral cells of the enamel organ had now extended outside of the bud. E45: The typical cap stage for this molar did not appear until E45. At this time, the entire enamel looked like a cap (Figure 1F, J). More notable cell differentiation was present than at E40. Four cell types were identified; outer enamel epithelium, inner enamel epithelium, stellate reticulum, and dental papilla. The dental sac could also be observed. E50: E50 embryos showed the typical appearance of the early bell stage of this molar (Figure 1K, O). The dental papilla was larger than during the cap stage, whereas there were no morphological changes of dental papilla cells. The cusp morphology could be seen at the junction of the inner enamel epithelium and dental papilla. Inner enamel epithelial cells near the cusp region became stylolitic in shape, with the nucleolus far from the basalis. The stellate reticulum had sufficiently developed and the stratum intermedium appeared between the inner enamel epithelium and the stellate reticulum. E55: At this stage, there were no further changes except the adoption of a highly stylolitic shape by the inner enamel epithelial cells near the cusp region (Figure 1L, P). E60: By E60, the deciduous molar had reached the late bell stage of development (Figure 1M, Q). In the cusp region, dental epithelial cells and mesenchymal cells were polarized, and the cells lengthened to become pre-ameloblast and pre-odontoblast. At the same time, the pink matrix was seen in the cusp region. E65: At E65, continuous and intact ameloblasts, enamel, dentin, and odontoblasts were observed in the molar cusp (Figure 1N, R).
Taken together, the crown development of miniature pigs’ mandibular deciduous molar were divided into five main periods as follows (Figure 1B): the dental lamina stage (E33-E35), bud stage (E35-E40), cap stage (E40-E50), early bell stage (E50-E60), and late bell stage (E60-E65). The relatively typical time points are E35 (bud), E45 (cap), E50 (early bell), and E60 (late bell).
Verification of gene expression
cDNA library overview
Crown development in the miniature pig’s mandibular deciduous molars could be divided into four relatively typical periods as noted above. The mandibular deciduous molar germ cells were excised from miniature pig embryos at the E35, E45, E50, and E60 time points.
A summary of ESTs and unigene analysis
Total number of EST sequences
Number of high quality sequences
Number of singletons
Number of contigs
Number of unigenes
Number of unigenes with BLAST hits
Number of unknown unigenes
Unigene sequence analysis
Based on BLAST results, 78.3% (10,883) of the unigenes were annotated to known genes, and 62.2% (6,772) had a BLAST score greater than 200. There were 3,024 unknown unigenes (21.7%) in the cDNA library. Unigenes whose sequences were markedly similar to known important proteins associated with dental development were found in this library, including ameloblastin, amelogenin, enamelin, dspp, and dmp1 (Additional file 6). What’s more, expression of known specific transcription factors (Additional file 7), growth factors (Additional file 8), and related receptors (Additional file 9) during murine tooth development also can be searched in the cDNA library. These results indicated that the cDNA library will be useful in facilitating further dental experiments in the miniature pig model.
Partial unigenes with high homology to Homo sapiens known genes
Homo sapiens cytoplasmic polyadenylation element binding protein 2 (CPEB2), transcript variant F, mRNA
Homo sapiens zinc finger E-box binding homeobox 2 (ZEB2) on chromosome 2
Homo sapiens TGF-beta activated kinase 1/MAP3K7 binding protein 3 (TAB3), mRNA
Homo sapiens splicing factor, arginine/serine-rich 12 (SFRS12), transcript variant 2, mRNA
Homo sapiens zinc finger protein 407 (ZNF407) on chromosome 18
Homo sapiens SATB homebox 2 (SATB2) on chromosome 2
Homo sapiens SAPS domain family, member 3 (SAPS3), transcript variant 3, mRNA
Homo sapiens LUC7-like 3 (S. cerevisiae) (LUC7L3), transcript variant 1, mRNA
Homo sapiens fibronectin type III and SPRY domain containing 1-like (FSD1L), transcript variant 3, mRNA
Homo sapiens nebulette (NEBL), transcript variant 3, mRNA
Homo sapiens formin-like 3 (FMNL3), transcript variant 2, mRNA
Homo sapiens fat mass and obesity associated (FTO) on chromosome 16
Homo sapiens Rho GTPase activating protein 19, mRNA (cDNA clone MGC:138804IMAGE:40082327) complete cds
Homo sapiens zinc finger CCCH-type containing 6 (ZC3H6), mRNA
Homo sapiens TEA domain family member 1 (SV40 transcriptional enhancer factor) (TEAD1), mRNA
Homo sapiens zinc finger and BTB domain containing 34 (ZBTB34), mRNA
Homo sapiens neuronal PAS domain protein 3 (NPAS3) on chromosome 14
Homo sapiens SIX homeobox 1 (SIX1) on chromosome 14
Homo sapiens B-cell CLL/lymphoma 11A (zinc finger protein) (BCL11A) on chromosome2
Homo sapiens TAR DNA binding protein (TARDPB) on chromosome 1
Homo sapiens protease, serine, 12 (neurotrupsin, motopsin) (PRSS12), mRNA
Homo sapiens fibroblast growth factor 14 (FGF14) on chromosome 13
Homo sapiens forkhead box D3 (FOX3D) on chromosome 1
cDNA expression patterns during tooth development
Up-regulated genes from E45 to E60 highly conserved homologous with known Homo sapiens genes
gi|119599067|schwannomin interacting protein 1, isoform CRA_c [Homo sapiens]
gi|169161838|similar to hCG2040565 [Homo sapiens]
gi|254911081|SH3 and multiple ankyrin repeat domains 2 (SHANK2), transcript variant 2, mRNAC1 [Homo sapiens]
gi|119604964|hypothetical protein MGC2747, isoform CRA_c [Homo sapiens]
gi|119588946|hCG1992991, isoform CRA_a [Homo sapiens]
gi|119574191|hCG1983891 [Homo sapiens]
gi|10834656|PP2281 [Homo sapiens]
gi|7959776|PRO1489 [Homo sapiens]
gi|221046286|unnamed protein product [Homo sapiens]
gi|226528280|short coiled-coil protein isoform 1 [Homo sapiens]
gi|187957136|LOC730130 protein [Homo sapiens]
gi|6653742|7h3 protein [Homo sapiens]
Down-regulated genes from E45 to E60 highly conserved homologous with known Homo sapiens genes
gi|37953286| transforming growth factor, beta 2 (TGFB2) [Homo sapiens]
gi|62897645|eukaryotic translation elongation factor 1 alpha 1 variant [Homo sapiens]
gi|119625564|hCG1820575 [Homo sapiens]
gi|168984469|retinoblastoma binding protein 7 [Homo sapiens]
gi|14211889|protein dpy-30 homolog [Homo sapiens]
gi|119627667|poly(A) binding protein, cytoplasmic 4 (inducible form), isoform CRA_b [Homo sapiens]
gi|4507797|ubiquitin-conjugating enzyme E2v2 [Homo sapiens]
gi|242380880|hypothetical protein [Homo sapiens]
gi|34533983|unnamed protein product [Homo sapiens]
gi|166014265|enabled-like protein variant hMenaDv6 [Homo sapiens]
gi|158256424|unnamed protein product [Homo sapiens]
gi|4929627|CGI-79 protein [Homo sapiens]
gi|211904140|DAZ-associated protein 2 isoform c [Homo sapiens]
gi|119578911|nuclear transcription factor, X-box binding 1, isoform CRA_a [Homo sapiens]
gi|119609186|nucleolar protein 1, 120kDa [Homo sapiens]
Genes only expressed in Homo sapiens during the tooth development course of miniature pigs
In the present study, we constructed a cDNA library from miniature pig molar tissue over the period of tooth development. We then confirmed the fold change of gene expression using qRT-PCR. Using large-scale sequencing and ESTs assemblage, a large pool of unigenes were found in this library. A total of 13,907 unigenes were assembled from 17,520 ESTs, indicating that redundancy was only 20.6%. Furthermore, 95% of these Unigenes contain only one or two ESTs, indicating the positive effect of cDNA library normalization, which can be used to identify expressed genes in the future.
Great progress has been made in the study of molecular mechanisms during tooth morphogenesis in the past 20 years, and most data were derived from studies on rodent embryos . However, owing to its similarity to human anatomy and physiology, pig models are superior in many aspects for the study of human development, diseases, and pre-clinical therapies [4–6]. Both domestic pigs and miniature pigs can be used in medical experimentation, but miniature pigs have many advantages, including an inherently small size, early sexual maturity, rapid breeding, and ease of management [25, 26]. The deciduous molar in the Chinese experimental miniature pig is oblong in shape and has five or six main cusps. It is bigger and has different morphology compared with all other deciduous teeth in the mandible, and it lies on the end of mandible body. All these characteristics contribute to being able to easily and accurately distinguish and isolate the tooth germ. There are high correlations between the deciduous and permanent teeth . Therefore, the deciduous molar was chosen as the first model tooth to evaluate in miniature pig tooth development.
There is little information concerning tooth development in large animal models [23, 24]. Some sequences in this cDNA library had high similarity with proteins associated with dental development such as ameloblastin, amelogenin, enamelin, dspp, and dmp1 [28–31]. Many genes involved in tooth development remain to be identified. For example, unigenes with high homology to known Homo sapiens genes in this library included FOXD3, SATB2, ZEB2 (Zinc finger E-box-binding homeobox 2 gene), etc. FOXD3, a member of the forkhead family of transcriptional regulations, plays a role in maintaining the epiblast and its derivatives and in establishing pluripotent ESC lines . SATB2 is a recently cloned member of the family of special AT-rich binding proteins. Satb2-/-mice exhibit both craniofacial abnormalities that resemble those observed in humans carrying a SATB2 translocation and defects in osteoblast differentiation and function . ZEB2 has been involved in Mowat-Wilson syndrome (MWS), a multiple congenital anomaly syndrome characterized by a distinct facial phenotype. MWS is caused by heterozygous mutations or deletions in ZEB2 .
Data from this study will facilitate further dental experiments in the miniature pig model. In the present study, we found that 12 up-regulated and 15 down-regulated genes may be involved in the miniature pig’s tooth development. We also found 6 down-regulated (DPY30, ENAH, BORA, DAZAP2, NOP2, and DDX24) and 2 up-regulated genes (SHANK2 and CAMK2N1) in miniature pigs with higher homology to Homo sapiens genes compared with those in the mouse. SHANK2 is a member of the Shank family of synaptic proteins that function as molecular scaffolds in the postsynaptic density . CAMK2N1 (calcium/calmodulin-dependent protein kinase II) expresses at high levels in osteogenic cells, and may be a good marker of osteogenic differentiation in mesenchymal stem cells . There is very little known about these genes and their roles in tooth development. Investigating the functions of these genes in tooth development in a swine model and humans will be of great interest.
In summary, we evaluated the histological features of miniature pigs’ deciduous molar development and identified five primary phases. A miniature pig embryo tooth cDNA library was constructed, which contains approximately 3.0 × 105 cfu with 17,520 high quality EST sequences and 13,907 unigenes. The established cDNA library provides the basis for further tooth development studies using this animal model.
Our results not only identify the specific transcriptome and cDNA profile in developing mandibular deciduous molars of the miniature pig, but also provide useful information for investigating the molecular mechanism of tooth development in the miniature pig.
Availability of supporting data
The supporting data is available in the Genebank. The library accession numbers is LIBEST_028375. And the Library name is developing mandibular deciduous molars of the miniature pig cDNA library.
This work was supported by Ministry of Science and Technology of China, and was funded by the National Program on Key Basic Research Project of China No. 2007CB947304 and 2010CB944801. The authors declare that they have no competing interest.
- Larsen MO, Rolin B: Use of the Gottingen miniature as a model of diabetes, with special focus on type 1 diabetes research. ILAR J. 2004, 45 (3): 303-313. 10.1093/ilar.45.3.303.View ArticlePubMedGoogle Scholar
- Schultze-Mosgau S, Schliephake H, Radespiel-Troger M, Neukam FW: Osseointegration of endodontic end-osseous cones: zirconium oxide vs titanurm. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2000, 89 (1): 91-98. 10.1016/S1079-2104(00)80022-0.View ArticlePubMedGoogle Scholar
- Chen L, Shi Q, Scharf SM: Hemodynamic effects of periodic obstructive apneas in sedated pigs with congestive heart failure. J Appl Physiol. 2000, 88 (3): 1051-1060.PubMedGoogle Scholar
- Dixon JA, Spinale FG: Large animal models of heart failure: a critical link in the translation of basic science to clinical practice. Circ Heart Fail. 2009, 2 (3): 262-271. 10.1161/CIRCHEARTFAILURE.108.814459.PubMed CentralView ArticlePubMedGoogle Scholar
- Markert M, Koschany A, Lueth T: Tracking of the liver for navigation in open surgery. Int J Comput Assist Radiol Surg. 2010, 5 (3): 229-235. 10.1007/s11548-009-0395-x.View ArticlePubMedGoogle Scholar
- van der Spoel TI, Agostoni P, van Belle E, Gyöngyösi M, Sluijter JP, Cramer MJ, Doevendans PA, Chamuleau SA, Jansen of Lorkeers SJ: Human relevance of pre-clinical studies in stem cell therapy: systematic review and meta-analysis of large animal models of ischaemic heart disease. Cardiovasc Res. 2011, 91 (4): 649-658. 10.1093/cvr/cvr113.View ArticlePubMedGoogle Scholar
- Bermejo A, Gonzalez O, Gonzalez JM: The pig as an animal model for experimentation on the temporomandibular articular complex. Oral Surg Oral Med Oral Pathol. 1993, 75 (1): 18-23. 10.1016/0030-4220(93)90399-O.View ArticlePubMedGoogle Scholar
- Ruehe B, Niehues S, Heberer S, Nelson K: Miniature pigs as an animal model for implant research: bone regeneration in critical-size defects. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2009, 108 (5): 699-706. 10.1016/j.tripleo.2009.06.037.View ArticlePubMedGoogle Scholar
- Wang SL, Liu Y, Fang D, Shi S: The miniature pig: a useful large animal model for dental and orofacial research. Oral Dis. 2007, 13 (6): 530-537. 10.1111/j.1601-0825.2006.01337.x.View ArticlePubMedGoogle Scholar
- Büchter A, Kleinheinz J, Wiesmann HP, Kersken J, Nienkemper M, Weyhrother H, Joos U, Meyer U: Biological and biomechanical evaluation of bone remodelling and implant stability after using an osteotome technique. Clin Oral Implants Res. 2005, 16 (1): 1-8.View ArticlePubMedGoogle Scholar
- Nkenke E, Lehner B, Fenner M, Roman FS, Thams U, Neukam FW, Radespiel-Tröger M: Immediate versus delayed loading of dental implants in the maxillae of miniatures: follow-up of implant stability and implant failures. Int J Oral Maxillofac Implants. 2005, 20 (1): 39-47.PubMedGoogle Scholar
- Sonoyama W, Liu Y, Fang D, Yamaza T, Seo BM, Zhang C, Liu H, Stan G, Wang CY, Shi S, Wang S: Mesenchymal stem cell-mediated functional tooth regeneration in Swine. PLoS One. 2012, 1 (1): 79-92.View ArticleGoogle Scholar
- Gao RT, Yan X, Zheng CY, Goldsmith CM, Afione A, Hai B, Xu JJ, Zhou J, Zhang CM, Chiorini JA, Baum BJ, Wang SL: AAV2-mediated transfer of the human aquaporin-1 cDNA restores fluid secretion from irradiated miniature pig parotid glands. Gene Ther. 2011, 18 (1): 38-42. 10.1038/gt.2010.128.PubMed CentralView ArticlePubMedGoogle Scholar
- Xu JJ, Zheng ZM, Fang DJ, Gao RT, Liu Y, Fan ZP, Zhang CM, Shi ST, Wang SL: Mesenchymal stromal cell-based treatment of jaw osteoradionecrosis in swine. Cell Transplant. 2012, 21 (8): 1679-1686. 10.3727/096368911X637434.View ArticlePubMedGoogle Scholar
- Li YS, Xu JJ, Mao LS, Liu Y, Gao RT, Zheng ZM, Chen WJ, Le A, Shi ST, Wang SL: Allogeneic mesenchymal stem cell-based therapy for bisphosphonate-related osteonecrosis of the jaw in swine. Stem Cells Dev. 2013, 22 (14): 2047-2056. 10.1089/scd.2012.0615.PubMed CentralView ArticlePubMedGoogle Scholar
- Wei F, Song T, Ding G, Xu J, Liu Y, Liu D, Fan Z, Zhang C, Shi S, Wang S: Functional tooth restoration by allogeneic mesenchymal stem cell-based bio-root regeneration in Swine. Stem Cells Dev. 2013, 22 (12): 1752-1762. 10.1089/scd.2012.0688.PubMed CentralView ArticlePubMedGoogle Scholar
- Thesleff I, Sharpe P: Signalling networks regulating dental development. Mech Dev. 1997, 67 (2): 111-123. 10.1016/S0925-4773(97)00115-9.View ArticlePubMedGoogle Scholar
- Thesleff I: Epithelial-mesenchymal signalling regulating tooth morphogenesis. J Cell Sci. 2003, 116: 1647-1648. 10.1242/jcs.00410.View ArticlePubMedGoogle Scholar
- Tucker A, Sharpe P: The cutting-edge of mammalian development; how the embryo makes teeth. Nat Rev Genet. 2004, 5 (7): 499-508. 10.1038/nrg1380.View ArticlePubMedGoogle Scholar
- Fleischmannova J, Matalova E, Tucker AS, Sharpe P: Mouse models of tooth abnormalities. Eur J Oral Sci. 2008, 116 (1): 1-10. 10.1111/j.1600-0722.2007.00504.x.View ArticlePubMedGoogle Scholar
- Li A, Song TL, Wang F, Liu DY, Fan ZP, Cheng S, Zhang CM, He JQ, Wang SL: MicroRNAome and expression profile of developing tooth germ in miniature pigs. PLoS One. 2012, 7 (12): e52256-10.1371/journal.pone.0052256.PubMed CentralView ArticlePubMedGoogle Scholar
- Wang F, Xiao J, Cong W, Li A, Song T, Wei F, Xu J, Zhang C, Fan Z, Wang S: Morphology and chronology of diphyodont dentition in miniature pigs, Sus Scrofa. Oral Oral Dis. 2014, 20 (4): 367-379. 10.1111/odi.12126.View ArticlePubMedGoogle Scholar
- Stembírek J, Buchtová M, Král T, Matalová E, Lozanoff S, Míšek I: Early morpho-genesis of heterodont dentition in miniature gigs. Eur J Oral Sci. 2010, 118 (6): 547-558. 10.1111/j.1600-0722.2010.00772.x.View ArticlePubMedGoogle Scholar
- Bivin WS, McClure RC: Deciduous tooth chronology in the mandible of the domestic pig. J Dent Res. 1976, 55 (4): 591-597. 10.1177/00220345760550040701.View ArticlePubMedGoogle Scholar
- England DC, Winters LM, Carpenter LE: The development of a breed of miniature swine; a preliminary report. Growth. 1954, 18 (4): 207-214.PubMedGoogle Scholar
- Weaver ME, Jump EB, McKean CF: The eruption pattern of permanent teeth in miniature swine. Arch Oral Biol. 1969, 14 (3): 323-331. 10.1016/0003-9969(69)90235-0.View ArticlePubMedGoogle Scholar
- Burdi AR, Superstine J: Developmental correlations of the deciduous and permanent teeth during the human fetal period. J Dent Res. 1977, 56 (12): 1468-10.1177/00220345770560120501.View ArticlePubMedGoogle Scholar
- Hirst KL, Simmons D, Feng J, Aplin H, Dixon MJ, MacDougall M: Elucidation of the sequence and the genomic organization of the human dentin matrix acidic phosphoprotein 1 (DMP1) gene: exclusion of the locus from a causative role in the pathogenesis of dentinogenesis imperfecta type II. Genomics. 1997, 42 (1): 38-45. 10.1006/geno.1997.4700.View ArticlePubMedGoogle Scholar
- Krebsbach PH, Lee SK, Matsuki Y, Kozak CA, Yamada KM, Yamada Y: Full-length sequence, localization, and chromosomal mapping of ameloblastin: a novel tooth-specific gene. J Biol Chem. 1996, 271 (8): 4431-4435. 10.1074/jbc.271.8.4431.View ArticlePubMedGoogle Scholar
- MacDougall M, Simmons D, Luan X, Nydegger J, Feng J, Gu TT: Dentin phosphoprotein and dentin sialoprotein are cleavage products expressed from a single transcript coded by a gene on human chromosome 4: dentin phosphoprotein DNA sequence determination. J Biol Chem. 1997, 272 (2): 835-842. 10.1074/jbc.272.2.835.View ArticlePubMedGoogle Scholar
- Iijima M, Fan D, Bromley KM, Sun Z, Moradian-Oldak J: Tooth enamel proteins enamelin and amelogenin cooperate to regulate the growth morphology of octacalcium phosphate crystals. Cryst Growth Des. 2010, 10 (11): 4815-4822. 10.1021/cg100696r.PubMed CentralView ArticlePubMedGoogle Scholar
- Pohl BS, Knöchel W, Of Fox and Frogs: Fox (fork head/winged helix) transcription factors in Xenopus development. Gene. 2005, 344: 21-32.View ArticlePubMedGoogle Scholar
- Dobreva G, Chahrour M, Dautzenberg M, Chirivella L, Kanzler B, Fariñas I, Karsenty G, Grosschedl R: SATB2 is a multifunctional determinant of craniofacial patterning and osteoblast differentiation. Cell. 2006, 125 (5): 971-986. 10.1016/j.cell.2006.05.012.View ArticlePubMedGoogle Scholar
- Garavelli L, Mainardi PC: Mowat-Wilson syndrome. Orphanet J Rare Dis. 2007, 2: 42-10.1186/1750-1172-2-42.PubMed CentralView ArticlePubMedGoogle Scholar
- Lim S, Naisbitt S, Yoon J, Hwang JI, Suh PG, Sheng M, Kim E: Characterization of the Shank family of synaptic proteins. Multiple genes, alternative splicing, and differential expression in brain and development. J Biol Chem. 1999, 74 (41): 29510-29518.View ArticleGoogle Scholar
- Ng F, Boucher S, Koh S, Sastry KS, Chase L, Lakshmipathy U, Choong C, Yang Z, Vemuri MC, Rao MS, Tanavde V: PDGF, TGF-beta, and FGF signaling is important for differentiation and growth of mesenchymal stem cells (MSCs): transcriptional profiling can identify markers and signaling pathways important in differentiation of MSCs into adipogenic, chondrogenic, and osteogenic lineages. Blood. 2008, 112 (2): 295-307. 10.1182/blood-2007-07-103697.View ArticlePubMedGoogle Scholar
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