用于胚胎着床研究的生物打印人子宫内膜激素反应双层模型。

IF 5.4 2区 医学 Q2 MATERIALS SCIENCE, BIOMATERIALS
Liora Jacobs Catane, Erez Asher, Reuven Reich, Tali Tavor Re'em
{"title":"用于胚胎着床研究的生物打印人子宫内膜激素反应双层模型。","authors":"Liora Jacobs Catane, Erez Asher, Reuven Reich, Tali Tavor Re'em","doi":"10.1021/acsbiomaterials.4c02473","DOIUrl":null,"url":null,"abstract":"<p><p>Implantation failure is a major challenge in reproductive medicine, with two-thirds of cases attributed to poor uterine receptivity. Current models have limited utility in capturing the complexities of the endometrium. This study introduces a novel bioprinted endometrial model with epithelial and stromal cells in a bilayer structure, designed to replicate the hormone-regulated endometrial environment and support embryo implantation studies. Alginate-based bioink formulations, cross-linked with calcium chloride or calcium gluconate, were optimized for 3D cell bioprinting, based on key parameters: reduced spreading ratio, lower printed line width standard deviation (SD), slower degradation rates, and enhanced cell viability. Human endometrial epithelial (RL95-2) and stromal (T HESCs) cell lines were encapsulated in the bioink and bioprinted in a bilayer structure: Clear stratification mimicking the layered architecture of native endometrium was confirmed using fluorescent microscopy. Sequential hormonal treatments with estradiol (proliferative phase), followed by estradiol and progesterone (secretory phase) highlighted the model's hormone-responsiveness. Estradiol significantly enhanced cell viability by day 2, while progesterone reduced cell viability by day 5, consistent with adaptation to the proliferative and secretory phases. Hormone-treated constructs displayed significantly lower E-cadherin expression, higher mRNA expression of various integrins and of vascular endothelial growth factor (VEGF), and reduced metalloproteinase (MMP)-2 secretion after 5 days, mirroring in vivo endometrial remodeling under progesterone influence. JAR spheroids, representing human blastocyst cells, adhered to and infiltrated the epithelial layer of the hormone-treated, bilayered model, effectively simulating embryo implantation. This bioprinted bilayer endometrial model represents a significant advancement in reproductive biology. It offers a platform for studying in vitro endometrial receptivity and implantation and paves the way for personalized treatment approaches in recurrent implantation failure.</p>","PeriodicalId":8,"journal":{"name":"ACS Biomaterials Science & Engineering","volume":"11 5","pages":"2922-2934"},"PeriodicalIF":5.4000,"publicationDate":"2025-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12077402/pdf/","citationCount":"0","resultStr":"{\"title\":\"Bioprinted Hormone-Responsive Bilayer Model of Human Endometrium for Embryo Implantation Studies.\",\"authors\":\"Liora Jacobs Catane, Erez Asher, Reuven Reich, Tali Tavor Re'em\",\"doi\":\"10.1021/acsbiomaterials.4c02473\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Implantation failure is a major challenge in reproductive medicine, with two-thirds of cases attributed to poor uterine receptivity. Current models have limited utility in capturing the complexities of the endometrium. This study introduces a novel bioprinted endometrial model with epithelial and stromal cells in a bilayer structure, designed to replicate the hormone-regulated endometrial environment and support embryo implantation studies. Alginate-based bioink formulations, cross-linked with calcium chloride or calcium gluconate, were optimized for 3D cell bioprinting, based on key parameters: reduced spreading ratio, lower printed line width standard deviation (SD), slower degradation rates, and enhanced cell viability. Human endometrial epithelial (RL95-2) and stromal (T HESCs) cell lines were encapsulated in the bioink and bioprinted in a bilayer structure: Clear stratification mimicking the layered architecture of native endometrium was confirmed using fluorescent microscopy. Sequential hormonal treatments with estradiol (proliferative phase), followed by estradiol and progesterone (secretory phase) highlighted the model's hormone-responsiveness. Estradiol significantly enhanced cell viability by day 2, while progesterone reduced cell viability by day 5, consistent with adaptation to the proliferative and secretory phases. Hormone-treated constructs displayed significantly lower E-cadherin expression, higher mRNA expression of various integrins and of vascular endothelial growth factor (VEGF), and reduced metalloproteinase (MMP)-2 secretion after 5 days, mirroring in vivo endometrial remodeling under progesterone influence. JAR spheroids, representing human blastocyst cells, adhered to and infiltrated the epithelial layer of the hormone-treated, bilayered model, effectively simulating embryo implantation. This bioprinted bilayer endometrial model represents a significant advancement in reproductive biology. It offers a platform for studying in vitro endometrial receptivity and implantation and paves the way for personalized treatment approaches in recurrent implantation failure.</p>\",\"PeriodicalId\":8,\"journal\":{\"name\":\"ACS Biomaterials Science & Engineering\",\"volume\":\"11 5\",\"pages\":\"2922-2934\"},\"PeriodicalIF\":5.4000,\"publicationDate\":\"2025-05-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12077402/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Biomaterials Science & Engineering\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.1021/acsbiomaterials.4c02473\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/5/1 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Biomaterials Science & Engineering","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1021/acsbiomaterials.4c02473","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/5/1 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0

摘要

着床失败是生殖医学的主要挑战,三分之二的病例归因于子宫接受性差。目前的模型在捕捉子宫内膜的复杂性方面效用有限。本研究介绍了一种具有双层结构的上皮细胞和基质细胞的新型生物打印子宫内膜模型,旨在复制激素调节的子宫内膜环境并支持胚胎植入研究。通过与氯化钙或葡萄糖酸钙交联的藻酸盐基生物墨水配方,优化了3D细胞生物打印的关键参数:降低扩散比,降低打印线宽标准差(SD),减慢降解率,增强细胞活力。将人子宫内膜上皮(RL95-2)和间质(T HESCs)细胞系包封在生物墨水中,并以双层结构进行生物打印:荧光显微镜证实了模拟天然子宫内膜分层结构的清晰分层。依次用雌二醇(增殖期),然后用雌二醇和黄体酮(分泌期)进行激素治疗,突出了模型的激素反应性。雌二醇在第2天显著提高了细胞活力,而黄体酮在第5天降低了细胞活力,这与细胞对增殖期和分泌期的适应一致。激素处理的构建体在5天后显著降低E-cadherin的表达,提高各种整合素和血管内皮生长因子(VEGF) mRNA的表达,减少金属蛋白酶(MMP)-2的分泌,反映了孕激素影响下的体内子宫内膜重塑。代表人囊胚细胞的JAR球体粘附并浸润激素处理的双层模型的上皮,有效地模拟胚胎着床。这种生物打印双层子宫内膜模型代表了生殖生物学的重大进展。它为研究子宫内膜容受性和着床提供了一个平台,并为复发性着床失败的个性化治疗铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bioprinted Hormone-Responsive Bilayer Model of Human Endometrium for Embryo Implantation Studies.

Implantation failure is a major challenge in reproductive medicine, with two-thirds of cases attributed to poor uterine receptivity. Current models have limited utility in capturing the complexities of the endometrium. This study introduces a novel bioprinted endometrial model with epithelial and stromal cells in a bilayer structure, designed to replicate the hormone-regulated endometrial environment and support embryo implantation studies. Alginate-based bioink formulations, cross-linked with calcium chloride or calcium gluconate, were optimized for 3D cell bioprinting, based on key parameters: reduced spreading ratio, lower printed line width standard deviation (SD), slower degradation rates, and enhanced cell viability. Human endometrial epithelial (RL95-2) and stromal (T HESCs) cell lines were encapsulated in the bioink and bioprinted in a bilayer structure: Clear stratification mimicking the layered architecture of native endometrium was confirmed using fluorescent microscopy. Sequential hormonal treatments with estradiol (proliferative phase), followed by estradiol and progesterone (secretory phase) highlighted the model's hormone-responsiveness. Estradiol significantly enhanced cell viability by day 2, while progesterone reduced cell viability by day 5, consistent with adaptation to the proliferative and secretory phases. Hormone-treated constructs displayed significantly lower E-cadherin expression, higher mRNA expression of various integrins and of vascular endothelial growth factor (VEGF), and reduced metalloproteinase (MMP)-2 secretion after 5 days, mirroring in vivo endometrial remodeling under progesterone influence. JAR spheroids, representing human blastocyst cells, adhered to and infiltrated the epithelial layer of the hormone-treated, bilayered model, effectively simulating embryo implantation. This bioprinted bilayer endometrial model represents a significant advancement in reproductive biology. It offers a platform for studying in vitro endometrial receptivity and implantation and paves the way for personalized treatment approaches in recurrent implantation failure.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
ACS Biomaterials Science & Engineering
ACS Biomaterials Science & Engineering Materials Science-Biomaterials
CiteScore
10.30
自引率
3.40%
发文量
413
期刊介绍: ACS Biomaterials Science & Engineering is the leading journal in the field of biomaterials, serving as an international forum for publishing cutting-edge research and innovative ideas on a broad range of topics: Applications and Health – implantable tissues and devices, prosthesis, health risks, toxicology Bio-interactions and Bio-compatibility – material-biology interactions, chemical/morphological/structural communication, mechanobiology, signaling and biological responses, immuno-engineering, calcification, coatings, corrosion and degradation of biomaterials and devices, biophysical regulation of cell functions Characterization, Synthesis, and Modification – new biomaterials, bioinspired and biomimetic approaches to biomaterials, exploiting structural hierarchy and architectural control, combinatorial strategies for biomaterials discovery, genetic biomaterials design, synthetic biology, new composite systems, bionics, polymer synthesis Controlled Release and Delivery Systems – biomaterial-based drug and gene delivery, bio-responsive delivery of regulatory molecules, pharmaceutical engineering Healthcare Advances – clinical translation, regulatory issues, patient safety, emerging trends Imaging and Diagnostics – imaging agents and probes, theranostics, biosensors, monitoring Manufacturing and Technology – 3D printing, inks, organ-on-a-chip, bioreactor/perfusion systems, microdevices, BioMEMS, optics and electronics interfaces with biomaterials, systems integration Modeling and Informatics Tools – scaling methods to guide biomaterial design, predictive algorithms for structure-function, biomechanics, integrating bioinformatics with biomaterials discovery, metabolomics in the context of biomaterials Tissue Engineering and Regenerative Medicine – basic and applied studies, cell therapies, scaffolds, vascularization, bioartificial organs, transplantation and functionality, cellular agriculture
×
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:481959085
Book学术官方微信