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1.
J Dent Res ; 91(2): 197-202, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22095070

ABSTRACT

Branching morphogenesis is essential for the formation of salivary glands, kidneys, lungs, and many other organs during development, but the mechanisms underlying this process are not adequately understood. Microarray and other gene expression methods have been powerful approaches for identifying candidate genes that potentially regulate branching morphogenesis. However, functional validation of the proposed roles for these genes has been severely hampered by the absence of efficient techniques to genetically manipulate cells within embryonic organs. Using ex vivo cultured embryonic mouse submandibular glands (SMGs) as models to study branching morphogenesis, we have identified new vectors for viral gene transfer with high efficiency and cell-type specificity to developing SMGs. We screened adenovirus, lentivirus, and 11 types of adeno-associated viruses (AAV) for their ability to transduce embryonic day 12 or 13 SMGs. We identified two AAV types, AAV2 and bovine AAV (BAAV), that are selective in targeting expression differentially to SMG epithelial and mesenchymal cell populations, respectively. Transduction of SMG epithelia with self-complementary (sc) AAV2 expressing fibroblast growth factor 7 (Fgf7) supported gland survival and enhanced SMG branching morphogenesis. Our findings represent, to our knowledge, the first successful selective gene targeting to epithelial vs. mesenchymal cells in an organ undergoing branching morphogenesis.


Subject(s)
Genes, Viral/genetics , Salivary Glands/embryology , Adenoviridae/genetics , Animals , Cattle , Cell Culture Techniques , Cell Line , Dependovirus/genetics , Epithelial Cells/physiology , Feasibility Studies , Fibroblast Growth Factor 7/genetics , Gene Expression Regulation, Developmental/genetics , Gene Transfer Techniques , Genes, Reporter/genetics , Genetic Vectors/genetics , Green Fluorescent Proteins/genetics , HEK293 Cells , Humans , Lentivirus/genetics , Luminescent Agents , Mesoderm/cytology , Mice , Morphogenesis/genetics , Organ Culture Techniques , Plasmids/genetics , Tissue Survival/genetics , Transduction, Genetic/methods , Transfection
2.
J Dent Res ; 90(9): 1078-84, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21709141

ABSTRACT

During organ development, local changes in gene expression govern morphogenesis and cell fate. We have generated a microanatomical atlas of epithelial gene expression of embryonic salivary glands. The mouse submandibular salivary gland first appears as a single mass of epithelial cells surrounded by mesenchyme, and it undergoes rapid branching morphogenesis to form a complex secretory organ with acini connected to an extensive ductal system. Using laser capture microdissection, we collected samples from 14 distinct epithelial locations at embryonic days 12.5, 13.5, 14, and 15, and characterized their gene expression by microarray analysis. These microarray results were evaluated by qPCR of biological replicates and by comparisons of the gene expression dataset with published expression data. Using this gene expression atlas to search for novel regulators of branching morphogenesis, we found a substantial reduction in mRNA levels of GSK3ß at the base of forming clefts. This unexpected finding was confirmed by immunostaining, and inhibition of GSK3ß activity enhanced salivary gland branching. This first microanatomical expression atlas of a developing gland characterizes changes in local gene expression during salivary gland development and differentiation, which should facilitate the identification of key genes involved in tissue morphogenesis.


Subject(s)
Databases, Genetic , Gene Expression Regulation, Developmental , Glycogen Synthase Kinase 3/physiology , Organogenesis/genetics , Submandibular Gland/embryology , Animals , Chromosome Mapping , Down-Regulation , Epithelial Cells/physiology , Gene Expression Profiling , Glycogen Synthase Kinase 3/genetics , Glycogen Synthase Kinase 3 beta , Mice , Mice, Inbred ICR , Microdissection/methods , Oligonucleotide Array Sequence Analysis , Organ Culture Techniques , Signal Transduction
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