In Vitro Toxicity Assessment of Emitted Materials Collected during the Manufacture of Water Pipe Plastic Linings
Supporting Files
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June 12 2019
File Language:
English
Details
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Alternative Title:Inhal Toxicol
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Personal Author:
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Description:US water infrastructure is in need of widespread repair due to age-related deterioration. Currently, the cured-in-place (CIPP) procedure is the most common method for water pipe repair. This method involves the on-site manufacture of a new polymer composite plastic liner within the damaged pipe. The CIPP process can release materials resulting in occupational and public health concerns. To understand hazards associated with CIPP-related emission exposures, an | toxicity assessment was performed. | Mouse alveolar epithelial and alveolar macrophage cell lines and condensates collected at 3 worksites utilizing styrene-based resins were utilized for evaluations. All condensate samples were normalized based on the major emission component, styrene. Further, a styrene-only exposure group was used as a control to determine mixture related toxicity. | Cytotoxicity differences were observed between worksite samples, with the CIPP worksite 4 sample inducing the most cell death. A proteomic evaluation was performed, which demonstrated styrene-, worksite-, and cell-specific alterations. This examination of protein expression changes determined potential biomarkers of exposure including transglutaminase 2, advillin, collagen type 1, perilipin-2, and others. Pathway analysis of exposure-induced proteomic alterations identified MYC and p53 to be regulators of cellular responses. Protein changes were also related to pathways involved in cell damage, immune response, and cancer. | Together these findings demonstrate potential risks associated with the CIPP procedure as well as variations between worksites regarding emissions and toxicity. Our evaluation identified biological pathways that require a future evaluation and also demonstrates that exposure assessment of CIPP worksites should examine multiple chemical components beyond styrene, as many cellular responses were styrene-independent.
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Subjects:
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Source:Inhal Toxicol. 31(4):131-146
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Pubmed ID:31187656
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Pubmed Central ID:PMC6639800
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Document Type:
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Funding:
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Volume:31
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Issue:4
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Collection(s):
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Main Document Checksum:urn:sha256:d0f38ab468e11bda4f9b6800f37be461c557b88025ad829f7c0a74eab3070be5
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Download URL:
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File Type:
Supporting Files
File Language:
English
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