Mouse Periodontal Ligament Fibroblasts

Cat.No.: CSC-C5412S

Species: Mouse

Source: Periodontal Ligament; Periodontium

Cell Type: Fibroblast

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Cat.No.
CSC-C5412S
Description
The periodontal ligament is composed of dense connective tissue and contains nerves, blood vessels, lymphocytes and epithelial cells. Periodontal ligament fibroblasts are the most important cells in the periodontal ligament, and their function is to participate in the synthesis and absorption of collagen, so that the collagen in the periodontal ligament can be continuously renewed.
Mouse periodontal ligament fibroblasts from Creative Bioarray are isolated from the mouse tooth tissue. The method we use to isolate mouse periodontal ligament fibroblasts was developed based on a combination of established and our proprietary methods. The mouse periodontal ligament fibroblasts are characterized by immunofluorescence with antibodies specific to vimentin or fibronectin. Each vial contains 0.5x10^6 cells per ml and is delivered frozen.
Species
Mouse
Source
Periodontal Ligament; Periodontium
Cell Type
Fibroblast
Disease
Normal
Quality Control
Mouse Periodontal Ligament Fibroblasts are negative for HIV-1, HBV, HCV, mycoplasma, bacteria, yeast and fungi.
Storage and Shipping
Creative Bioarray ships frozen cells on dry ice. On receipt, immediately transfer frozen cells to liquid nitrogen (-180 °C) until ready for experimental use. Never can cells be kept at -20 °C.
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.

Mouse Periodontal Ligament Fibroblasts (MPDLFs) are fibroblast-like cells that have been isolated from periodontal ligament (PDL) tissue of mice. The PDL itself is a specialized connective tissue that helps support the tooth from the surrounding alveolar bone and distribute mechanical load during biting and chewing before remodeling tissue components. MPDLFs serve as an in vitro model system for periodontal biology and disease.

Mouse Periodontal Ligament Fibroblasts in culture are spindle-shaped and form adherent monolayers. As expected of fibroblasts, they express vimentin and produce collagen type I, collagen type III and fibronectin. Depending on stimulation conditions, these cells can also express markers associated with osteogenic or cementogenic differentiation, such as alkaline phosphatase (ALP), Runx2, and osteocalcin, reflecting the regenerative potential of periodontal ligament tissue. MPDLFs have been used extensively to study periodontal inflammation and tissue remodeling, orthodontic tooth movement, and alveolar bone regeneration. MPDLFs upregulate proliferation, cytokine secretion, and matrix production when stimulated by mechanical stress, bacterial products (such as lipopolysaccharide), and pro-inflammatory cytokines. Due to these properties they have also been used to study signaling cascades related to inflammation and remodeling such as NF-κB, MAPK and TGF-β.

Migration in mPDLFs is Dependent on P.g-LPS Induced Nlrp3 Inflammasome

Inflammasomes initiate inflammatory responses to danger signals, but their role in chronic periodontitis, particularly in periodontal ligament fibroblasts (PDLFs), remains unclear. Lian's team demonstrated abundant Nlrp3 inflammasome component expression in cultured mouse PDLFs (mPDLFs).

RT-PCR and Western blot confirmed mRNA and protein expression of NLRP3, ASC, and Caspase-1 in mPDLFs (Fig. 1A-F). While Porphyromonas gingivalis LPS (P.g-LPS) is known to compromise PDLF functions including migration, its specific regulatory role was unexplored. They found that P.g-LPS markedly decreased mPDLF migration without causing cytotoxicity (Fig. 2A-C). Importantly, the Nlrp3 inflammasome inhibitor ISO recovered P.g-LPS-induced migration dysfunction (Fig. 2D, E), indicating that the Nlrp3 pathway mediates P.g-LPS-induced migration impairment in mPDLFs.

The mPDLFs express Nlrp3,ASC and pro-Caspase1 mRNA and protein.

Fig. 1. The mPDLFs express Nlrp3,ASC and pro-Caspase1 mRNA and protein (Lian D, Dai L, et al., 2020).

Fibrocytes migrate to wound sites in vivo.

Fig. 2. Fibrocytes migrate to wound sites in vivo (Lian D, Dai L, et al., 2020).

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