HISTOCHEMICAL AND IMMUNOHISTOCHEMICAL FEATURES OF DIFFERENTIATED TROPHOBLAST IN CHORIONIC VILLI OF THE PLACENTA IN PRETERM LABOR

P. Tokar
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To determine certain histochemical and immunohistochemical characteristics of proteins in the trophoblast of theintermediate and terminal chorionic villi of the placenta in preterm labor.Material and Methods. The obtained material (30 placentas from preterm deliveries and 30 placentas from normalpregnancies) was fi xed for 20-24 hours in 10 % neutral formalin solution buff ered in Lilly’s phosphate buff er. After tissue removal, the placental tissue was dehydrated in an ascending ethanol series and embedded in paraffi n at a temperature of approximately 58 °C. Serial histologic sections were cut at 5.0 μm thickness using an MS-2 sliding microtome. After deparaffi nization, histological sections were stained with hematoxylin and eosin, histochemical methods for total protein with bromophenol blue according to Bonhéme, and immunohistochemical techniques according to the manufacturer’s protocols (Dako, Denmark). In particular, immunohistochemical reactions were performed with monoclonal antibodies against trophoblast hormone- placental lactogen and placental alkaline phosphatase. Visualization of primary antibodies was performed using the Dako polymer visualization system with diaminobenzidine as chromogen (resulting in brown staining of the sites of studied antigens). In addition to the descriptive method of histopathologic research, computer morphometry of digital microphotographs of histologic sections was performed using a Delta Optical Evolution 100 microscope and an Olympus SP550UZ digital camera. Digital copies of the images were processed using a legitimate copy of the ImageJ v1.52f computer program developed for histometric studies (National Institutes of Health, USA). Specifi cally, the evaluation of staining intensity (optical density) was performed on digital microphotographs using the method of computer microdensitometry. For this purpose, a microprobe method was used to obtain a computer brightness value in an 8-bit analysis system with 256 gray levels – from black (0) to white (255).The obtained values were then transformed into relative optical density values (r.OD) by logarithmic transformation (naturallogarithm method). The relative optical density value ranges from 0 (absolute transparency of the object) to 1 (absolute opacity of the object). The obtained digital data were processed using statistical analysis methods. A legitimate copy of the statistical analysis computer program PAST v4.14 was used, with a preliminary check for normal distribution using the Shapiro- Wilk test. Since, according to this test, the hypothesis of normal distribution was not rejected for the statistical samples studied (at p=0.05), parametric methods of statistical analysis were applied: calculation of the mean and its standard error, Student’s t-test (two-tailed, unpaired). In addition, the non-parametric Mann- Whitney test was used for the reliability of the conclusions. The research was conducted as part of the scientifi c research project «Preservation and Restoration of Reproductive Health in Women and Girls with Obstetric and Gynecological Pathology» at the Department of Obstetrics and Gynecology of Bukovinian State Medical University (state registration number 0121U110020, duration 2021-2025).Results. Microscopic examination of histological sections stained with hematoxylin and eosin did not reveal any diff erencesin the structure of chorionic villus trophoblast in the placenta of preterm labor compared to normal pregnancy. However,histochemical and immunohistochemical methods of investigation revealed a number of features in the trophoblast of chorionic villi, where fundamental events related to substance exchange occur – intermediate immature, intermediate mature, terminal villi, including terminal «specialized villi».Conclusions. According to the obtained histochemical and immunohistochemical data, in preterm labor, compared to normalpregnancy, no changes are observed in the trophoblast of intermediate immature villi, while in intermediate mature and terminal villi, there is a decrease in histochemical staining for total protein and immunohistochemical staining for specifi c trophoblast proteins – placental lactogen hormone and placental alkaline phosphatase enzyme.","PeriodicalId":162458,"journal":{"name":"Neonatology, surgery and perinatal medicine","volume":"199 S588","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neonatology, surgery and perinatal medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.24061/2413-4260.xiv.1.51.2024.12","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The importance of studying the histochemical and immunohistochemical features of the diff erentiated trophoblast in chorionic villi of the placenta in preterm labor is determined by the threatening nature of this condition for both mother and fetus, as well as its high prevalence and serious consequences for the health of both. The understanding of the damage to the trophoblast of chorionic villi in the placenta can be expanded by histochemical and immunohistochemical methods, which allow the assessment of the concentration of specifi c marker molecules in one way or another.Objective. To determine certain histochemical and immunohistochemical characteristics of proteins in the trophoblast of theintermediate and terminal chorionic villi of the placenta in preterm labor.Material and Methods. The obtained material (30 placentas from preterm deliveries and 30 placentas from normalpregnancies) was fi xed for 20-24 hours in 10 % neutral formalin solution buff ered in Lilly’s phosphate buff er. After tissue removal, the placental tissue was dehydrated in an ascending ethanol series and embedded in paraffi n at a temperature of approximately 58 °C. Serial histologic sections were cut at 5.0 μm thickness using an MS-2 sliding microtome. After deparaffi nization, histological sections were stained with hematoxylin and eosin, histochemical methods for total protein with bromophenol blue according to Bonhéme, and immunohistochemical techniques according to the manufacturer’s protocols (Dako, Denmark). In particular, immunohistochemical reactions were performed with monoclonal antibodies against trophoblast hormone- placental lactogen and placental alkaline phosphatase. Visualization of primary antibodies was performed using the Dako polymer visualization system with diaminobenzidine as chromogen (resulting in brown staining of the sites of studied antigens). In addition to the descriptive method of histopathologic research, computer morphometry of digital microphotographs of histologic sections was performed using a Delta Optical Evolution 100 microscope and an Olympus SP550UZ digital camera. Digital copies of the images were processed using a legitimate copy of the ImageJ v1.52f computer program developed for histometric studies (National Institutes of Health, USA). Specifi cally, the evaluation of staining intensity (optical density) was performed on digital microphotographs using the method of computer microdensitometry. For this purpose, a microprobe method was used to obtain a computer brightness value in an 8-bit analysis system with 256 gray levels – from black (0) to white (255).The obtained values were then transformed into relative optical density values (r.OD) by logarithmic transformation (naturallogarithm method). The relative optical density value ranges from 0 (absolute transparency of the object) to 1 (absolute opacity of the object). The obtained digital data were processed using statistical analysis methods. A legitimate copy of the statistical analysis computer program PAST v4.14 was used, with a preliminary check for normal distribution using the Shapiro- Wilk test. Since, according to this test, the hypothesis of normal distribution was not rejected for the statistical samples studied (at p=0.05), parametric methods of statistical analysis were applied: calculation of the mean and its standard error, Student’s t-test (two-tailed, unpaired). In addition, the non-parametric Mann- Whitney test was used for the reliability of the conclusions. The research was conducted as part of the scientifi c research project «Preservation and Restoration of Reproductive Health in Women and Girls with Obstetric and Gynecological Pathology» at the Department of Obstetrics and Gynecology of Bukovinian State Medical University (state registration number 0121U110020, duration 2021-2025).Results. Microscopic examination of histological sections stained with hematoxylin and eosin did not reveal any diff erencesin the structure of chorionic villus trophoblast in the placenta of preterm labor compared to normal pregnancy. However,histochemical and immunohistochemical methods of investigation revealed a number of features in the trophoblast of chorionic villi, where fundamental events related to substance exchange occur – intermediate immature, intermediate mature, terminal villi, including terminal «specialized villi».Conclusions. According to the obtained histochemical and immunohistochemical data, in preterm labor, compared to normalpregnancy, no changes are observed in the trophoblast of intermediate immature villi, while in intermediate mature and terminal villi, there is a decrease in histochemical staining for total protein and immunohistochemical staining for specifi c trophoblast proteins – placental lactogen hormone and placental alkaline phosphatase enzyme.
早产儿胎盘绒毛中分化滋养细胞的组织化学和免疫组化特征
研究早产儿胎盘绒毛中不同分化滋养细胞的组织化学和免疫组化特征的重要性,是由这种情况对母亲和胎儿的威胁性、高发病率以及对二者健康的严重后果所决定的。通过组织化学和免疫组化方法,可以以某种方式评估特定标记分子的浓度,从而加深对胎盘中绒毛滋养层受损情况的了解。确定早产儿胎盘中间和末端绒毛滋养层蛋白质的组织化学和免疫组化特征。将获得的材料(30 个早产胎盘和 30 个正常妊娠胎盘)在 10 % 的中性福尔马林溶液中浸泡 20-24 小时,并在礼来磷酸盐缓冲液中缓冲。取出组织后,胎盘组织在乙醇升温系列中脱水,并在约 58 °C 的温度下嵌入石蜡。使用 MS-2 滑动显微切片机切取厚度为 5.0 μm 的连续组织切片。去蜡后,用苏木精和伊红对组织切片进行染色,按照 Bonhéme 的方法用溴酚蓝对总蛋白进行组织化学染色,并按照生产商(丹麦 Dako 公司)的方案进行免疫组化技术处理。特别是用针对滋养层激素-胎盘泌乳素和胎盘碱性磷酸酶的单克隆抗体进行免疫组化反应。使用 Dako 聚合物显像系统对一抗进行显像,用二氨基联苯胺作为显色剂(使研究的抗原位点呈棕色染色)。除了组织病理学研究的描述性方法外,还使用台达光学 Evolution 100 显微镜和奥林巴斯 SP550UZ 数码相机对组织切片的数码显微照片进行了计算机形态测量。图像的数字拷贝使用为组织计量学研究开发的 ImageJ v1.52f 计算机程序(美国国立卫生研究院)的正版拷贝进行处理。具体来说,对数码显微照片的染色强度(光密度)评估是采用计算机显微密度计的方法进行的。为此,使用微探针方法在 8 位分析系统中获得计算机亮度值,该系统有 256 个灰度级--从黑色(0)到白色(255)。相对光学密度值的范围从 0(物体绝对透明)到 1(物体绝对不透明)。获得的数字数据使用统计分析方法进行处理。使用了 PAST v4.14 统计分析计算机程序的正版拷贝,并使用 Shapiro- Wilk 检验法对正态分布进行了初步检查。根据该检验,所研究的统计样本未拒绝正态分布假设(P=0.05),因此采用了参数统计分析方法:计算平均数及其标准误差、学生 t 检验(双尾、非配对)。此外,还使用了非参数曼-惠特尼检验来确定结论的可靠性。该研究是布科维尼亚国立医科大学妇产科系(国家注册号 0121U110020,期限 2021-2025)"保护和恢复患有妇产科病症的妇女和女孩的生殖健康 "科研项目的一部分。经苏木精和伊红染色的组织切片显微镜检查显示,早产胎盘中绒毛滋养层的结构与正常妊娠相比没有任何差异。然而,通过组织化学和免疫组化方法的研究发现了绒毛滋养层的一些特征,其中发生了与物质交换有关的基本事件--中间不成熟绒毛、中间成熟绒毛、末端绒毛,包括末端 "特化绒毛"。根据所获得的组织化学和免疫组化数据,与正常妊娠相比,早产的中间未成熟绒毛滋养层没有发生变化,而在中间成熟绒毛和末端绒毛中,总蛋白的组织化学染色和滋养层特异蛋白--胎盘泌乳素和胎盘碱性磷酸酶的免疫组化染色均有所下降。
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