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Leucine rich amelogenin peptide alters ameloblast differentiation in vivo

Authors
 Jonathan Stahl  ;  Yukiko Nakano  ;  Seong-Oh Kim  ;  Carolyn W. Gibson  ;  Thuan Le  ;  Pamela DenBesten 
Citation
 MATRIX BIOLOGY, Vol.32(7-8) : 432-442, 2013 
Journal Title
 MATRIX BIOLOGY 
ISSN
 0945-053X 
Issue Date
2013
MeSH
Ameloblasts/drug effects ; Ameloblasts/physiology* ; Amelogenesis/physiology* ; Animals ; Cell Differentiation/drug effects* ; Cell Differentiation/physiology ; DNA Primers/genetics ; Dental Enamel Proteins/pharmacology* ; Gene Expression Regulation/drug effects* ; Gene Expression Regulation/physiology ; Histological Techniques ; Immunohistochemistry ; In Situ Hybridization ; In Situ Nick-End Labeling ; Matrix Attachment Region Binding Proteins/metabolism ; Matrix Metalloproteinase 20/metabolism ; Mice ; Mice, Knockout ; Mice, Transgenic ; Polymerase Chain Reaction ; X-Ray Microtomography
Keywords
Ameloblasts ; Amelogenin ; Enamel ; LRAP ; Leucine rich amelogenin peptide (LRAP) ; MMP20 ; SATB1 ; Transgenic mice ; leucine rich amelogenin peptide ; matrix metalloproteinase 20
Abstract
Highly mineralized tooth enamel develops from an extracellular matrix chiefly comprised of amelogenins formed by splicing of 7 (human) or 9 (rodent) exons secreted from specialized epithelial cells known as ameloblasts. Here we examined the role of the 59 amino acid alternatively spliced amelogenin known as leucine rich amelogenin peptide (LRAP) on enamel formation, using transgenic murine models in which LRAP overexpression is driven by an amelogenin promoter (TgLRAP). Beginning in the secretory stage of mouse amelogenesis, we found a reduced thickness of enamel matrix and a loss of Tomes' processes, followed by upregulated amelogenin mRNA expression, inhibited amelogenin secretion and loss of cell polarity. In the presecretory stage (P0) amelogenin m180 mRNA expression was increased 58 fold along with a 203 fold increase in MMP-20 expression and 3.5 and 3.2 fold increased in respectively enamelin and ameloblastin. When LRAP was overexpressed on an amelogenin knockout mouse model, the ameloblasts were not affected. Further, expression of the global chromatin organizer and transcription factor SATB1 was reduced in secretory stage TgLRAP ameloblasts. These findings identify a cellular role for LRAP in enamel formation that is not directly related to directing enamel crystal formation as is reported to be the primary function of full length amelogenins. The effect of LRAP overexpression in upregulating amelogenins, MMP-20 and SATB1, suggests a role in protein regulation critical to ameloblast secretion and matrix processing, to form a mineralized enamel matrix.
Full Text
http://www.sciencedirect.com/science/article/pii/S0945053X13000905
DOI
10.1016/j.matbio.2013.05.004
Appears in Collections:
2. College of Dentistry (치과대학) > Dept. of Pediatric Dentistry (소아치과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Seong Oh(김성오) ORCID logo https://orcid.org/0000-0002-8620-1377
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/89278
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