n-Butyl Benzyl Phthalate Exposure Promotes Lesion Survival in a Murine Endometriosis Model
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n-Butyl benzyl phthalate exposure in mice increased endometriotic lesion survival by enhancing CD44 expression on plasmacytoid dendritic cells, which are crucial for lesion growth.
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Abstract
Endometriosis is an inflammatory and estrogen-dependent gynecological disease associated with exposure to environmental endocrine disruptors. n-Butyl benzyl phthalate (BBP), a ubiquitous plasticizer, has weak estrogenic activity, and exposure to BBP is associated with endometriosis. We aimed to elucidate the immunomodulatory effect of BBP on endometriosis development. We previously established a surgery-induced endometriosis-like murine model. In the present study, we exposed those mice to BBP 10 days prior to surgery and 4 weeks after surgery at physiologically relevant doses to mimic human exposure. Chronic exposure to BBP did not promote the growth of endometriotic lesions; however, the lesion survival rate in BBP-treated mice did increase significantly compared with control mice. Multiparametric flow cytometry showed that BBP exposure did not affect the homeostasis of infiltrated immune subsets in lesions but did enhance CD44 (adhesion marker) expression on plasmacytoid dendritic cells (pDCs). Blocking CD44 interactions locally inhibited endometriotic lesion growth. Immunofluorescence results further confirmed that CD44 blocking inhibited pDC infiltration and reduced the frequency of CD44+ pDCs in endometriotic tissues. BBP also disrupted the estrus cycle in these mice. This study suggests that chronic exposure to low-dose BBP may promote survival of endometriotic tissue through CD44-expressing pDCs.
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References (45)
- A Novel Mouse Model of Endometriosis Mimics Human Phenotype and Reveals Insights into the Inflammatory Contribution of Shed Endometrium via openalex
- A prominent environmental endocrine disruptor, 4-nonylphenol, promotes endometriosis development via plasmacytoid dendritic cells via openalex
- Cadmium a metalloestrogen: are we convinced? via openalex
- Decoy receptor 3 promotes cell adhesion and enhances endometriosis development via openalex
- Dendritic cell populations in the eutopic and ectopic endometrium of women with endometriosis via openalex
- Dendritic cells support angiogenesis and promote lesion growth in a murine model of endometriosis via openalex
- Endometriosis via openalex
- Endometriosis, a disease of the macrophage via openalex
- Endometriosis: pathogenesis and treatment via openalex
- General gynaecology: Association of phthalate esters with endometriosis in Indian women via openalex
- IL‐10 from plasmacytoid dendritic cells promotes angiogenesis in the early stage of endometriosis via openalex
- IL-27 triggers IL-10 production in Th17 cells via a c-Maf/RORγt/Blimp-1 signal to promote the progression of endometriosis via openalex
- Pathogenesis and pathophysiology of endometriosis via openalex
- Phthalates and risk of endometriosis via openalex
- Rediscovering peritoneal macrophages in a murine endometriosis model via openalex
- Retrograde menstruation in healthy women and in patients with endometriosis. via openalex
- Serum Level of IL-10 Is Increased in Patients with Endometriosis, and IL-10 Promotes the Growth of Lesions in a Murine Model via openalex
- The development of endometriosis in a murine model is dependent on the presence of dendritic cells via openalex
- W2593246118 via openalex
- W2765440201 via openalex
- W2809833821 via openalex
- W2884952568 via openalex
- W2990363563 via openalex
- W6628680024 via openalex
- W6667078964 via openalex
- W6684406552 via openalex
- W6718734304 via openalex
- W6729593217 via openalex
- W1975575462 via openalex
- W1975995958 via openalex
- W2010936172 via openalex
- W2027741236 via openalex
- W2030644918 via openalex
- W2041454621 via openalex
- W2042124938 via openalex
- W2065994341 via openalex
- W2073181168 via openalex
- W2074909265 via openalex
- W2078130324 via openalex
- W2086181263 via openalex
- W2098275650 via openalex
- W2105005092 via openalex
- W2145683716 via openalex
- W2163119252 via openalex
- W2460364093 via openalex
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