Segmentation of placental tissue using immunofluorescent staining and an artificial intelligence-based analysis workflow.

IF 3.2 2区 生物学 Q2 REPRODUCTIVE BIOLOGY
Rebecca Reif, Stephanie K Yanow, Denise G Hemmings
{"title":"Segmentation of placental tissue using immunofluorescent staining and an artificial intelligence-based analysis workflow.","authors":"Rebecca Reif, Stephanie K Yanow, Denise G Hemmings","doi":"10.1093/biolre/ioag201","DOIUrl":null,"url":null,"abstract":"<p><p>The placenta continuously remodels in response to maternal and fetal signals, with proteins dynamically regulated across placental regions. However, methods to evaluate proteins within these distinct regions are limited. To address this, we developed a placental tissue classifier to segment regions corresponding to the villous core, villous trophoblast (VT) and the intervillous space (IVS) using HALO AI imaging analysis. Tissue sections of biopsies from human term placentas embedded in OCT or paraffin (FFPE) were stained by immunofluorescence with antibodies to placental alkaline phosphatase (PLAP), syndecan-1 (SDC-1), vimentin or E-cadherin. The placental tissue classifier was trained using PLAP and DAPI staining with distinct image-feature patterns to distinguish VT from the villous core and the IVS on stained sections. The accuracy of HALO to measure area and intensity of staining in classified regions was demonstrated by staining for SDC-1 on VT and vimentin on stromal cells. As expected, SDC-1 staining was low in the villous core, and higher on VT than in the IVS, whereas vimentin staining was only detected in the villous core. By applying this analysis method to images collected by whole slide scanning microscopy, the area of staining was increased 245 times compared to a single field of view, which increases the probability of detecting pathological changes in different regions of the placenta. The advantages of using this validated classifier are the speed and accuracy of analysis across large tissue areas, the flexibility to detect other cell types, and to expand to single villi analysis.</p>","PeriodicalId":8965,"journal":{"name":"Biology of Reproduction","volume":" ","pages":""},"PeriodicalIF":3.2000,"publicationDate":"2026-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biology of Reproduction","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/biolre/ioag201","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"REPRODUCTIVE BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The placenta continuously remodels in response to maternal and fetal signals, with proteins dynamically regulated across placental regions. However, methods to evaluate proteins within these distinct regions are limited. To address this, we developed a placental tissue classifier to segment regions corresponding to the villous core, villous trophoblast (VT) and the intervillous space (IVS) using HALO AI imaging analysis. Tissue sections of biopsies from human term placentas embedded in OCT or paraffin (FFPE) were stained by immunofluorescence with antibodies to placental alkaline phosphatase (PLAP), syndecan-1 (SDC-1), vimentin or E-cadherin. The placental tissue classifier was trained using PLAP and DAPI staining with distinct image-feature patterns to distinguish VT from the villous core and the IVS on stained sections. The accuracy of HALO to measure area and intensity of staining in classified regions was demonstrated by staining for SDC-1 on VT and vimentin on stromal cells. As expected, SDC-1 staining was low in the villous core, and higher on VT than in the IVS, whereas vimentin staining was only detected in the villous core. By applying this analysis method to images collected by whole slide scanning microscopy, the area of staining was increased 245 times compared to a single field of view, which increases the probability of detecting pathological changes in different regions of the placenta. The advantages of using this validated classifier are the speed and accuracy of analysis across large tissue areas, the flexibility to detect other cell types, and to expand to single villi analysis.

使用免疫荧光染色和基于人工智能的分析工作流程分割胎盘组织。
胎盘在响应母体和胎儿的信号中不断重塑,在胎盘区域中动态调节蛋白质。然而,评估这些不同区域内蛋白质的方法是有限的。为了解决这个问题,我们开发了一个胎盘组织分类器,使用HALO AI成像分析来分割绒毛核心、绒毛滋养层(VT)和绒毛间隙(IVS)对应的区域。用OCT或石蜡包埋的人足月胎盘活检组织切片(FFPE)用胎盘碱性磷酸酶(PLAP)、syndecan-1 (SDC-1)、vimentin或E-cadherin抗体免疫荧光染色。使用具有不同图像特征模式的PLAP和DAPI染色训练胎盘组织分类器,以区分染色切片上的VT与绒毛核心和IVS。通过对间质细胞进行SDC-1染色和对间质细胞进行vimentin染色,证明了HALO测量分类区域染色面积和染色强度的准确性。正如预期的那样,SDC-1染色在绒毛中心较低,在VT上高于IVS,而vimentin染色仅在绒毛中心检测到。将该分析方法应用于全载片扫描显微镜采集的图像,染色面积比单视野增加了245倍,增加了检测胎盘不同区域病理变化的概率。使用这种经过验证的分类器的优点是跨大组织区域分析的速度和准确性,检测其他细胞类型的灵活性,并扩展到单个绒毛分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Biology of Reproduction
Biology of Reproduction 生物-生殖生物学
CiteScore
6.30
自引率
5.60%
发文量
214
审稿时长
1 months
期刊介绍: Biology of Reproduction (BOR) is the official journal of the Society for the Study of Reproduction and publishes original research on a broad range of topics in the field of reproductive biology, as well as reviews on topics of current importance or controversy. BOR is consistently one of the most highly cited journals publishing original research in the field of reproductive biology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书