Year: 2017
Type: article
Abstract: Preterm birth is the leading cause of neonatal mortality, and is frequently associated with intra-amniotic infection hypothesized to arise from bacterial ascension across a dysfunctional cervical mucus plug. To study this dysfunction, we assessed the permeability of cervical mucus from non-pregnant ovulating (n = 20) and high- (n = 9) and low-risk (n = 16) pregnant women to probes of varying sizes and surface chemistries. We found that the motion of negatively charged, carboxylated microspheres in mucus from pregnant patients was significantly restricted compared to ovulating patients, but not significantly different between high- and low-risk pregnant women. In contrast, charged peptide probes small enough to avoid steric interactions, but sensitive to the biochemical modifications of mucus components exhibited significantly different transport profiles through mucus from high- and low-risk patients. Thus, although both microstructural rearrangements of the components of mucus as well as biochemical modifications to their adhesiveness may alter the overall permeability of the cervical mucus plug, our findings suggest that the latter mechanism plays a dominant role in the impairment of the function of this barrier during preterm birth. We expect that these probes may be readily adapted to study the mechanisms underlying disease progression on all mucosal epithelia, including those in the mouth, lungs, and gut.
Source: Scientific Reports
Language: English
Subfield: Epidemiology
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $2,690
Funders: National Science Foundation, Materials Research Science and Engineering Center, Harvard University, Natural Sciences and Engineering Research Council of Canada, National Institute of General Medical Sciences, National Institute of Environmental Health Sciences, National Institute of Biomedical Imaging and Bioengineering, Division of Materials Research
Awards: Graduate Training in Computational and Systems Biology, Graduate Research Fellowship Program, G3725677605, Training Grant in Environmental Toxicology, G4917416065, Mucin Glycans in the Regulation of Microbial Virulence, MIT Materials Research Science and Engineering Center (MRSEC), CAREER: SELECTIVE TRANSPORT IN BIOLOGICAL HYDROGELS - FROM DESIGN PRINCIPLES TO MECHANISMS
OpenAlex ID: W2753292934
