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子宫内暴露于实验性母体哮喘会改变绵羊胎儿气道的发育。

In utero exposure to experimental maternal asthma alters fetal airway development in sheep.

作者信息

Hammond Sarah J, Roff Andrea J, Robinson Joshua L, Darby Jack R T, Meakin Ashley S, Clifton Vicki L, Bischof Robert J, Stark Michael J, Wallace Megan J, Tai Andrew, Morrison Janna L, Gatford Kathryn L

机构信息

Robinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.

School of Biomedicine, University of Adelaide, Adelaide, South Australia, Australia.

出版信息

Exp Physiol. 2025 Jun;110(6):899-907. doi: 10.1113/EP092502. Epub 2025 Jan 27.

DOI:10.1113/EP092502
PMID:39869487
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12128463/
Abstract

The mechanisms linking maternal asthma (MA) exposure in utero and subsequent risk of asthma in childhood are not fully understood. Pathological airway remodelling, including reticular basement membrane thickening, has been reported in infants and children who go on to develop asthma later in childhood. This suggests altered airway development before birth as a mechanism underlying increased risk of asthma in children exposed in utero to MA. We hypothesised that in utero MA exposure would reduce airway diameter and increase airway-associated smooth muscle area and reticular basement membrane thickness in neonatal offspring. Experimental MA was induced by maternal sensitisation followed by airway challenges with house dust mite before and during pregnancy. Lambs from control (n = 16) or MA (n = 26) ewes were delivered at ∼140 days gestation (term = 150 days), ventilated for 45 min, then humanely killed. Left lungs were inflation-fixed, and cross-sections of generation 2-5 airways were collected. Airway sections were stained with Haematoxylin and Eosin, Masson's Trichrome and Gordon and Sweet's histological stains for morphological analysis. Lamb body and lung weights were similar between groups (P > 0.5 and P > 0.7, respectively). Lambs that were exposed to MA had narrower airway diameters (P = 0.019) and thinner reticular basement membrane (P = 0.016) but similar airway-associated smooth muscle area (P = 0.152) compared with unexposed control lambs. Our results demonstrate a potential mechanism for increased risk of asthma in children of mothers with asthma, independent of genetic risk or behavioural changes during pregnancy.

摘要

子宫内母体哮喘(MA)暴露与儿童期后续哮喘风险之间的关联机制尚未完全明确。在后来儿童期发生哮喘的婴幼儿中,已报道存在包括网状基底膜增厚在内的病理性气道重塑。这表明出生前气道发育改变是子宫内暴露于MA的儿童哮喘风险增加的潜在机制。我们推测子宫内MA暴露会使新生后代气道直径减小,气道相关平滑肌面积增加,网状基底膜厚度增加。通过母体致敏,随后在怀孕前和怀孕期间用屋尘螨进行气道激发来诱导实验性MA。在妊娠约140天(足月为150天)时,分娩来自对照(n = 16)或MA(n = 26)母羊的羔羊,通气45分钟,然后实施安乐死。左肺经充气固定,收集第2 - 5代气道的横截面。气道切片用苏木精和伊红、Masson三色染色法以及Gordon和Sweet组织学染色法染色,用于形态学分析。两组之间羔羊的体重和肺重量相似(分别为P > 0.5和P > 0.7)。与未暴露的对照羔羊相比,暴露于MA的羔羊气道直径更窄(P = 0.019),网状基底膜更薄(P = 0.016),但气道相关平滑肌面积相似(P = 0.152)。我们的结果表明,哮喘母亲的孩子哮喘风险增加存在一种潜在机制,这与遗传风险或孕期行为变化无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e59a/12128463/99528acd14a6/EPH-110-899-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e59a/12128463/7fcc16060846/EPH-110-899-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e59a/12128463/583a5f44dfd6/EPH-110-899-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e59a/12128463/99528acd14a6/EPH-110-899-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e59a/12128463/7fcc16060846/EPH-110-899-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e59a/12128463/583a5f44dfd6/EPH-110-899-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e59a/12128463/99528acd14a6/EPH-110-899-g003.jpg

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BJOG. 2025 Jul;132(8):1045-1055. doi: 10.1111/1471-0528.17900. Epub 2024 Jul 8.
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