Effect of β-aminopropionitrile (BAPN) on matrix formation and collagen components produced by MC3T3-E1 cells.

(a) BAPN treatment did not affect the proliferation of MC cells, as demonstrated by MTS assay. (b) Expression of core-binding factor alpha 1/runt-related transcription factor 2 (Runx2/Cbfa1) and type I collagen α2 chain (Col1a2) did not change, while the levels of lysyl oxidase (Lox) were significantly elevated after BAPN treatment in a dose-dependent manner. (c) Collagen components were analyzed by electrophoresis. In the control, all chains (α, β, and γ) were clearly observable. However, BAPN treatment led to the inhibition of β- and γ-chain formation. Picrosirius Red staining was visualized under bright-field (d) and polarized light (e). Collagen quantity was not affected by BAPN, while the alignment of collagenous fibers and matrix maturation were impaired. Bar: 100 μm. (f) Collagen content was slightly increased following 0.5 mM BAPN treatment, but it decreased after the administration of 2 mM BAPN. Hyl/Hyp × 300 decreased after the treatment with 2 mM BAPN. Divalent DHLNL and HLNL levels decreased with 0.5 mM BAPN treatment and were not detectable following the treatment with 1.0 and 2.0 mM BAPN. Trivalent pyridinoline levels significantly decreased after the application of 0.5 mM BAPN, while they were undetectable following the treatment with 1.0 and 2.0 mM BAPN. *p < 0.05, compared to the control.</p

Morphometric analysis of femur.

Morphometric analysis of femur.</p

Effect of low cross-linked matrices on osteoblast and osteoclast.

(a) The ablation of cellular components by DOC was confirmed by DAPI staining. Bar: 50 μm. (b)The Lox activity of prepared matrices before and after the DOC treatment was analyzed. The Lox activity was significantly decreased in the matrices produced by BAPN-treated cells. DOC treatment did not significantly affect the Lox activity of prepared matrices, regardless of the BAPN concentration. (c) The proliferation of MC cells was significantly increased in the low cross-link density matrices. (d) Alkaline phosphatase (ALP) activity increased in cells seeded on low cross-linked matrices. (e) Gene expression of Cbfa1/Runx2, type I collagen α2 chain (Col1a2), alkaline phosphatase (Alpl), and osteocalcin (Spp1) significantly increased in these matrices at 3 and 7 days of culture. (f) Osteoclasts were cultured on differentially cross-linked matrices for 6 days under the differentiation condition. The number of multi-nuclear tartrate-resistant acid phosphatase (TRAP)-positive cells increased in the low cross-link density matrices. (g) Gene expression of cathepsin K (Ctsk), nuclear factor of activated T-cells cytoplasmic 1 (Nfatc1), and dendritic cell-specific transmembrane protein (DCstamp) increased in low cross-link density matrices. *p < 0.05, compared to the control.</p

Histological and histomorphometric analysis.

(a) Hematoxylin and eosin, and tartrate-resistant acid phosphatase (TRAP)-stained histological sections of the distal femur epiphysis at 0 week (after 8-week of the BAPN consumption). (b) No differences of osteoblast and osteoclasts activities were observed at 0 and 2 weeks after replacing to the control diet. After 4 weeks, number of osteoblasts per bone surface (N.Ob/BS) and osteoblast surface per bone surface (Ob.S/BS), representing osteoblast activity, significantly increased, while number of osteoclasts per bone surface (N.Oc/BS) and osteoclast surface per bone surface (Oc.S/BS), representing osteoclast activity did not change. *p < 0.05, compared to the control. Bar: 50 μm. (c) Picrosirius red-stained samples at 16 weeks of age (after 8-week of the BAPN consumption followed by 4-week of control diet) are analyzed under polarized light. After 4-week of control diet, immature/irregular collagen matrix still detected both in cortical and cancellous bone. Bar: 50 μm. Quantitative data also confirmed that the immature collagens, detected in green, retained high value after 4-week of control diet in cancellous bone.</p

Effect of low cross-linked matrices on osteoblastic differentiation of BMSCs.

(a) BMSCs to the prepared matrices was shown. Cell nuclei were stained using DAPI (blue), and the cytoskeleton was stained with phalloidin (red). Initial adhesion of cells cultured on low cross-link density matrix increased. (b) Proliferation of BMSCs was significantly elevated in low cross-linked matrices. (c) ALP activity of BMSCs increased in low cross-link density matrices. (d) Gene expression of Col1a2, Alpl, and Spp1 was significantly increased, while that of Cbfa1/Runx2 did not change in low cross-link density matrices after 1 and 2 weeks. *p < 0.05, compared to the control. Bars: 20 μm.</p

Effects of β-aminopropionitrile (BAPN)-containing diet on body weight, bone volume, and collagen cross-linking in mice.

(a) The body weight of mice increased steadily throughout the experimental period, and no differences were observed between groups. (b) Histology of Picrosirius Red-stained samples at 12 weeks of age (after 8-week of the BAPN consumption) is shown. Under polarized light, positive pixel ratio of immature matrix (green) increased with BAPN administration, while that of mature matrix (red) did not change Bar: 200 μm. (c) Collagen Cross-links were analyzed at 12 weeks of age (after 8-week of the BAPN consumption). Collagen content and hydroxylysine (Hyl)/hydroxyproline (Hyp) × 300 were not affected by BAPN, but dehydrodihydroxylysinonorleucine (DHLNL) and dehydrohydroxylysinonorleucine (HLNL) levels decreased in a dose-dependent manner. Pyridinoline, deoxypyridinoline, and total aldehyde contents were significantly reduced in mice fed with BAPN-containing diet. *p < 0.05, compared to the control.</p

DataSheet1_Extracellular Matrix-Oriented Proteomic Analysis of Periodontal Ligament Under Mechanical Stress.PDF

The periodontal ligament (PDL) is a specialized connective tissue that provides structural support to the tooth and is crucial for oral functions. The mechanical properties of the PDL are mainly derived from the tissue-specific composition and structural characteristics of the extracellular matrix (ECM). The ECM also plays key roles in determining cell fate in the cellular microenvironment thus crucial in the PDL tissue homeostasis. In the present study, we determined the comprehensive ECM profile of mouse molar PDL using laser microdissection and mass spectrometry-based proteomic analysis with ECM-oriented data curation. Additionally, we evaluated changes in the ECM proteome under mechanical loading using a mouse orthodontic tooth movement (OTM) model and analyzed potential regulatory networks using a bioinformatics approach. Proteomic changes were evaluated in reference to the novel second harmonic generation (SHG)-based fiber characterization. Our ECM-oriented proteomics approach succeeded in illustrating the comprehensive ECM profile of the mouse molar PDL. We revealed the presence of type II collagen in PDL, possibly associated with the load-bearing function upon occlusal force. Mechanical loading induced unique architectural changes in collagen fibers along with dynamic compositional changes in the matrisome profile, particularly involving ECM glycoproteins and matrisome-associated proteins. We identified several unique matrisome proteins which responded to the different modes of mechanical loading in PDL. Notably, the proportion of type VI collagen significantly increased at the mesial side, contributing to collagen fibrogenesis. On the other hand, type XII collagen increased at the PDL-cementum boundary of the distal side. Furthermore, a multifaceted bioinformatics approach illustrated the potential molecular cues, including PDGF signaling, that maintain ECM homeostasis under mechanical loading. Our findings provide fundamental insights into the molecular network underlying ECM homeostasis in PDL, which is vital for clinical diagnosis and development of biomimetic tissue-regeneration strategies.</p