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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Microproteome of dentoalveolar tissues

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Author(s):
Salmon, Cristiane R. ; Giorgetti, Ana Paula O. ; Paes Leme, Adriana F. ; Domingues, Romenia R. ; Kolli, Tamara N. ; Foster, Brian L. ; Nociti, Jr., Francisco H.
Total Authors: 7
Document type: Journal article
Source: BONE; v. 101, p. 219-229, AUG 2017.
Web of Science Citations: 7
Abstract

Proteomic analysis of extracellular matrices (ECM) of dentoalveolar tissues can provide insights into developmental, pathological, and reparative processes. However, targeted dissection of mineralized tissues, dental cementum (DC), alveolar bone (AB), and dentin (DE), presents technical difficulties. We demonstrate an approach combining EDTA decalcification and laser capture microdissection (LCM), followed by liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS), to analyze proteome profiles of these tissues. Using the LCM-LC-MS/MS approach, a total of 243 proteins was identified from all tissues, 193 proteins in DC, 147 in AB, and 135 proteins DE. Ninety proteins (37% of total) were common to all tissues, whereas 52 proteins (21%) were overlapping in only two. Also, 101 (42%) proteins were exclusively detected in DC (60), AB (15), or DE (26). Identification in all tissues of expected ECM proteins including collagen alpha-1(I) chain (COL1A1), collagen alpha-1 (XII) chain (COL12A1), biglycan (BGN), asporin (ASPN), lumican (LUM), and fibromodulin (FMOD), served to validate the approach. Principal component analysis (PCA) and hierarchical clustering identified a high degree of similarity in DC and AB proteomes, whereas DE presented a distinct dataset. Exclusively and differentially identified proteins were detected from all three tissues. The protein-protein interaction network (interactome) of DC was notable for its inclusion of several indicators of metabolic function (e.g. mitochondria] proteins, protein synthesis, and calcium transport), possibly reflecting cementocyte activity. The DE proteome included known and novel mineralization regulators, including matrix metalloproteinase 20 (MMP-20), 5' nucleotidase (NT5E), and secreted phosphoprotein 24 (SPP-24 or SPP-2). Application of the LCM-LC-MS/MS approach to dentoalveolar tissues would be of value in many experimental designs, including developmental studies of trans genic animals, investigation of treatment effects, and identification of novel regenerative factors. (C) 2017 Elsevier Inc. All rights reserved. (AU)

FAPESP's process: 10/12486-7 - Proteomic and gene expression comparative analysis of human dental cementum and alveolar bone.
Grantee:Cristiane Ribeiro Salmon
Support Opportunities: Scholarships in Brazil - Post-Doctoral