Potentiation of Adipogenesis by Reactive Oxygen Species is a Unifying Mechanism in the Pro-adipogenic Properties of Bisphenol A and its New Structural Analogues Article Swipe
Radha Dutt Singh
,
Jessica L. Wager
,
Taylor B. Scheidl
,
Liam Connors
,
Sarah Easson
,
Mikyla A. Callaghan
,
Samuel Alatorre-Hinojosa
,
Lucy Swift
,
Pina Colarusso
,
Anshul S. Jadli
,
Timothy E. Shutt
,
Vaibhav B. Patel
,
Jennifer Thompson
·
YOU?
·
· 2022
· Open Access
·
· DOI: https://doi.org/10.1101/2022.09.08.507176
YOU?
·
· 2022
· Open Access
·
· DOI: https://doi.org/10.1101/2022.09.08.507176
Aims Structural analogues of bisphenol A (BPA), including BPS and BPF, are emerging environmental toxicants as their presence in the environment is rising since new regulatory restrictions were placed on BPA-containing infant products. The adipogenesis-enhancing effect of bisphenols may explain the link between human exposure and metabolic disease; however, underlying molecular pathways remain unresolved. Results Exposure to BPS, BPF, BPA or ROS generators enhanced lipid droplet formation and expression of adipogenic markers after induction of differentiation in adipose-derived progenitors isolated from mice. RNAseq analysis in BPS-exposed progenitors revealed modulation in pathways regulating adipogenesis and responses to oxidative stress. ROS was higher in bisphenol-exposed cells, while co-treatment with antioxidants attenuated adipogenesis and abolished the effect of BPS. There was a loss of mitochondria membrane potential in BPS-exposed cells and mitochondria-derived ROS contributed to potentiation of adipogenesis by BPS and its analogues. Male mice exposed to BPS during gestation had higher whole-body adiposity, as measured by TD-NMR, while postnatal exposure had no impact on adiposity in either sex. Innovation These findings support existing evidence showing a role for ROS in regulating adipocyte differentiation and are the first to highlight ROS as a unifying mechanism that explains the pro-adipogenic properties of BPA and its structural analogues. Conclusion ROS act as signaling molecules in the regulation of adipocyte differentiation and mediate bisphenol-induced potentiation of adipogenesis.
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Metadata
- Type
- preprint
- Language
- en
- Landing Page
- https://doi.org/10.1101/2022.09.08.507176
- https://www.biorxiv.org/content/biorxiv/early/2022/10/29/2022.09.08.507176.full.pdf
- OA Status
- green
- Cited By
- 3
- References
- 33
- Related Works
- 10
- OpenAlex ID
- https://openalex.org/W4297849081
All OpenAlex metadata
Raw OpenAlex JSON
- OpenAlex ID
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https://openalex.org/W4297849081Canonical identifier for this work in OpenAlex
- DOI
-
https://doi.org/10.1101/2022.09.08.507176Digital Object Identifier
- Title
-
Potentiation of Adipogenesis by Reactive Oxygen Species is a Unifying Mechanism in the Pro-adipogenic Properties of Bisphenol A and its New Structural AnaloguesWork title
- Type
-
preprintOpenAlex work type
- Language
-
enPrimary language
- Publication year
-
2022Year of publication
- Publication date
-
2022-09-08Full publication date if available
- Authors
-
Radha Dutt Singh, Jessica L. Wager, Taylor B. Scheidl, Liam Connors, Sarah Easson, Mikyla A. Callaghan, Samuel Alatorre-Hinojosa, Lucy Swift, Pina Colarusso, Anshul S. Jadli, Timothy E. Shutt, Vaibhav B. Patel, Jennifer ThompsonList of authors in order
- Landing page
-
https://doi.org/10.1101/2022.09.08.507176Publisher landing page
- PDF URL
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https://www.biorxiv.org/content/biorxiv/early/2022/10/29/2022.09.08.507176.full.pdfDirect link to full text PDF
- Open access
-
YesWhether a free full text is available
- OA status
-
greenOpen access status per OpenAlex
- OA URL
-
https://www.biorxiv.org/content/biorxiv/early/2022/10/29/2022.09.08.507176.full.pdfDirect OA link when available
- Concepts
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Adipogenesis, Reactive oxygen species, Adipocyte, Cell biology, Adipose tissue, Chemistry, Mitochondrion, Bisphenol A, Oxidative stress, Bisphenol, Endocrinology, Biology, Internal medicine, Biochemistry, Medicine, Epoxy, Organic chemistryTop concepts (fields/topics) attached by OpenAlex
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3Total citation count in OpenAlex
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2025: 1, 2024: 1, 2023: 1Per-year citation counts (last 5 years)
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33Number of works referenced by this work
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10Other works algorithmically related by OpenAlex
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| referenced_works_count | 33 |
| abstract_inverted_index.A | 6 |
| abstract_inverted_index.a | 119, 174, 190 |
| abstract_inverted_index.as | 16, 152, 189, 207 |
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| abstract_inverted_index.in | 19, 77, 85, 90, 102, 125, 164, 178, 210 |
| abstract_inverted_index.is | 22 |
| abstract_inverted_index.no | 160 |
| abstract_inverted_index.of | 4, 37, 70, 75, 115, 121, 134, 198, 213, 220 |
| abstract_inverted_index.on | 30, 162 |
| abstract_inverted_index.or | 61 |
| abstract_inverted_index.to | 57, 96, 132, 144, 186 |
| abstract_inverted_index.BPA | 60, 199 |
| abstract_inverted_index.BPS | 9, 137, 145 |
| abstract_inverted_index.ROS | 62, 99, 130, 177, 188, 205 |
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| abstract_inverted_index.its | 139, 201 |
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| abstract_inverted_index.the | 20, 41, 113, 184, 195, 211 |
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| abstract_inverted_index.BPS, | 58 |
| abstract_inverted_index.BPS. | 116 |
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| abstract_inverted_index.from | 81 |
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| abstract_inverted_index.role | 175 |
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| abstract_inverted_index.There | 117 |
| abstract_inverted_index.These | 168 |
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| abstract_inverted_index.first | 185 |
| abstract_inverted_index.human | 44 |
| abstract_inverted_index.lipid | 65 |
| abstract_inverted_index.mice. | 82 |
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| abstract_inverted_index.their | 17 |
| abstract_inverted_index.while | 105, 156 |
| abstract_inverted_index.(BPA), | 7 |
| abstract_inverted_index.RNAseq | 83 |
| abstract_inverted_index.cells, | 104 |
| abstract_inverted_index.during | 146 |
| abstract_inverted_index.effect | 36, 114 |
| abstract_inverted_index.either | 165 |
| abstract_inverted_index.higher | 101, 149 |
| abstract_inverted_index.impact | 161 |
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| abstract_inverted_index.placed | 29 |
| abstract_inverted_index.remain | 53 |
| abstract_inverted_index.rising | 23 |
| abstract_inverted_index.Results | 55 |
| abstract_inverted_index.TD-NMR, | 155 |
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| abstract_inverted_index.droplet | 66 |
| abstract_inverted_index.explain | 40 |
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| abstract_inverted_index.markers | 72 |
| abstract_inverted_index.mediate | 217 |
| abstract_inverted_index.showing | 173 |
| abstract_inverted_index.stress. | 98 |
| abstract_inverted_index.support | 170 |
| abstract_inverted_index.ABSTRACT | 0 |
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| abstract_inverted_index.disease; | 48 |
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| abstract_inverted_index.adipocyte | 180, 214 |
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| abstract_inverted_index.products. | 33 |
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| abstract_inverted_index.Conclusion | 204 |
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| abstract_inverted_index.whole-body | 150 |
| abstract_inverted_index.BPS-exposed | 86, 126 |
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| abstract_inverted_index.restrictions | 27 |
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| abstract_inverted_index.bisphenol-induced | 218 |
| abstract_inverted_index.mitochondria-derived | 129 |
| abstract_inverted_index.adipogenesis-enhancing | 35 |
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| cited_by_percentile_year.min | 89 |
| corresponding_author_ids | https://openalex.org/A5101917440 |
| countries_distinct_count | 2 |
| institutions_distinct_count | 13 |
| corresponding_institution_ids | https://openalex.org/I168635309, https://openalex.org/I25790992, https://openalex.org/I2802127220 |
| citation_normalized_percentile.value | 0.57209818 |
| citation_normalized_percentile.is_in_top_1_percent | False |
| citation_normalized_percentile.is_in_top_10_percent | False |