Please use this identifier to cite or link to this item: https://doi.org/10.1002/adhm.202202376
Title: Modeling Crevicular Fluid Flow and Host-Oral Microbiome Interactions in a Gingival Crevice-on-Chip
Authors: Makkar, Hardik
Zhou, Ying
Tan, Kai Soo 
Lim, Chwee Teck 
Sriram, Gopu 
Keywords: Science & Technology
Technology
Engineering, Biomedical
Nanoscience & Nanotechnology
Materials Science, Biomaterials
Engineering
Science & Technology - Other Topics
Materials Science
gingival crevices
gingival crevicular fluids
host-microbe interactions
microfluidics
organs-on-a-chip
periodontal disease
FUSOBACTERIUM-NUCLEATUM BIOFILM
INTERSTITIAL FLOW
A-CHIP
STAPHYLOCOCCUS-AUREUS
MORPHOGEN GRADIENTS
GLOBAL BURDEN
PERIODONTITIS
INFLAMMATION
PATHOGENESIS
DIFFERENTIATION
Issue Date: 28-Nov-2022
Publisher: WILEY
Citation: Makkar, Hardik, Zhou, Ying, Tan, Kai Soo, Lim, Chwee Teck, Sriram, Gopu (2022-11-28). Modeling Crevicular Fluid Flow and Host-Oral Microbiome Interactions in a Gingival Crevice-on-Chip. ADVANCED HEALTHCARE MATERIALS 12 (6). ScholarBank@NUS Repository. https://doi.org/10.1002/adhm.202202376
Abstract: Gingival crevice and gingival crevicular fluid (GCF) flow play a crucial role at the gingiva-oral microbiome interface which contributes toward maintaining the balance between gingival health and periodontal disease. Interstitial flow of GCF strongly impacts the host-microbiome interactions and tissue responses. However, currently available in vitro preclinical models largely disregard the dynamic nature of gingival crevicular microenvironment, thus limiting the progress in the development of periodontal therapeutics. Here, a proof-of-principle “gingival crevice-on-chip” microfluidic platform to culture gingival connective tissue equivalent (CTE) under dynamic interstitial fluid flow mimicking the GCF is described. On-chip co-culture using oral symbiont (Streptococcus oralis) shows the potential to recapitulate microbial colonization, formation of biofilm-like structures at the tissue-microbiome interface, long-term co-culture, and bacterial clearance secondary to simulated GCF (s-GCF) flow. Further, on-chip exposure of the gingival CTEs to the toll-like receptor-2 (TLR-2) agonist or periodontal pathogen Fusobacterium nucleatum demonstrates the potential to mimic early gingival inflammation. In contrast to direct exposure, the induction of s-GCF flow toward the bacterial front attenuates the secretion of inflammatory mediators demonstrating the protective effect of GCF flow. This proposed in vitro platform offers the potential to study complex host-microbe interactions in periodontal disease and the development of periodontal therapeutics under near-microphysiological conditions.
Source Title: ADVANCED HEALTHCARE MATERIALS
URI: https://scholarbank.nus.edu.sg/handle/10635/238905
ISSN: 2192-2640
2192-2659
DOI: 10.1002/adhm.202202376
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