Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/238906
Title: Differential immune responses of 3D gingival and periodontal connective tissue equivalents to microbial colonization
Authors: Makkar, Hardik
Atkuru, Srividya
Tang, Yi Ling
Sethi, Tanya
Lim, Chwee Teck 
Tan, Kai Soo 
Sriram, Gopu 
Keywords: Science & Technology
Life Sciences & Biomedicine
Cell & Tissue Engineering
Cell Biology
3D culture
tissue constructs
fibroblast heterogeneity
innate immune response
periodontopathogens
inflammatory cytokines
FUSOBACTERIUM-NUCLEATUM BIOFILM
NF-KAPPA-B
LIGAMENT FIBROBLASTS
INFLAMMATORY RESPONSE
EPITHELIAL-CELLS
EXPRESSION
LIPOPOLYSACCHARIDE
COMMENSAL
IL-6
HETEROGENEITY
Issue Date: 1-Jul-2022
Publisher: SAGE PUBLICATIONS INC
Citation: Makkar, Hardik, Atkuru, Srividya, Tang, Yi Ling, Sethi, Tanya, Lim, Chwee Teck, Tan, Kai Soo, Sriram, Gopu (2022-07-01). Differential immune responses of 3D gingival and periodontal connective tissue equivalents to microbial colonization. JOURNAL OF TISSUE ENGINEERING 13. ScholarBank@NUS Repository.
Abstract: Gingival and periodontal ligament fibroblasts are functionally distinct cell types within the dento-gingival unit that participate in host immune response. Their microenvironment influences the behavior and immune response to microbial challenge. We developed three-dimensional gingival and periodontal connective tissue equivalents (CTEs) using human fibrin-based matrix. The CTEs were characterized, and the heterogeneity in their innate immune response was investigated. The CTEs demonstrated no to minimal response to planktonic Streptococcus mitis and Streptococcus oralis, while their biofilms elicited a moderate increase in IL-6 and IL-8 production. In contrast, Fusobacterium nucleatum provoked a substantial increase in IL-6 and IL-8 production. Interestingly, the gingival CTEs secreted significantly higher IL-6, while periodontal counterparts produced higher IL-8. In conclusion, the gingival and periodontal CTEs exhibited differential responses to various bacterial challenges. This gives insights into the contribution of tissue topography and fibroblast heterogeneity in rendering protective and specific immune responses toward early biofilm colonizers.
Source Title: JOURNAL OF TISSUE ENGINEERING
URI: https://scholarbank.nus.edu.sg/handle/10635/238906
ISSN: 2041-7314
2041-7314
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