{"title":"三维图像分析量化细胞受体的时空表达","authors":"Sarmed Al-Samerria, G. Almahbobi","doi":"10.12720/JOMB.3.3.179-182","DOIUrl":null,"url":null,"abstract":"� Abstract≤O varian folliculogenesis is primarily controlled by the action of gonadotropins namely follicle stimulating hormone (FSH) and luteinizing hormone (L H). Several reports indicated that the process of initial recruitment of primordial follicles to the growing follicles is not gonadotropin-dependent but Bone morphogenetic protein (B M P)-dependent. However, this has not been unequivocally confirmed. T he aim of this study was to investigate the temporo-spacial protein expression of the B M P receptors 1B (B M PR1b), FSH R and L H R in several stages of follicle development. W hile the localization of all receptors was found in granulosa cell membrane of the follicles the temporal expression was varied. B M PR1b was expressed in all follicle stages, FSH R was detected in primary follicles onward and L H R was absent in both primordial and primary follicles but appeared in later stages. Q uantitative analysis based on the intensity of fluorescent signals showed that the expression of B M PR1b, FSH R and L H R significantly (p< 0.001 p< 0.0001 p< 0.0001 respectively) increased with follicular development. W e have concluded that the combination of sensitive immunofluorescence labeling and computerized 3D image analysis proves efficient tools for in situ detection and quantification of the expression of small amount of protein in a complex tissue structure.","PeriodicalId":437476,"journal":{"name":"Journal of medical and bioengineering","volume":"88 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"8","resultStr":"{\"title\":\"Three-Dimensional Image Analysis to Quantify the Temporo-Spacial Expression of Cellular Receptors\",\"authors\":\"Sarmed Al-Samerria, G. Almahbobi\",\"doi\":\"10.12720/JOMB.3.3.179-182\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"� Abstract≤O varian folliculogenesis is primarily controlled by the action of gonadotropins namely follicle stimulating hormone (FSH) and luteinizing hormone (L H). Several reports indicated that the process of initial recruitment of primordial follicles to the growing follicles is not gonadotropin-dependent but Bone morphogenetic protein (B M P)-dependent. However, this has not been unequivocally confirmed. T he aim of this study was to investigate the temporo-spacial protein expression of the B M P receptors 1B (B M PR1b), FSH R and L H R in several stages of follicle development. W hile the localization of all receptors was found in granulosa cell membrane of the follicles the temporal expression was varied. B M PR1b was expressed in all follicle stages, FSH R was detected in primary follicles onward and L H R was absent in both primordial and primary follicles but appeared in later stages. Q uantitative analysis based on the intensity of fluorescent signals showed that the expression of B M PR1b, FSH R and L H R significantly (p< 0.001 p< 0.0001 p< 0.0001 respectively) increased with follicular development. W e have concluded that the combination of sensitive immunofluorescence labeling and computerized 3D image analysis proves efficient tools for in situ detection and quantification of the expression of small amount of protein in a complex tissue structure.\",\"PeriodicalId\":437476,\"journal\":{\"name\":\"Journal of medical and bioengineering\",\"volume\":\"88 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1900-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"8\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of medical and bioengineering\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.12720/JOMB.3.3.179-182\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of medical and bioengineering","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12720/JOMB.3.3.179-182","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 8
摘要
≤0型卵泡发生主要受促性腺激素即促卵泡激素(FSH)和黄体生成素(L H)的作用控制。一些报道表明,原始卵泡向生长卵泡的初始募集过程不是促性腺激素依赖的,而是骨形态发生蛋白(B M P)依赖的。然而,这还没有得到明确的证实。本研究的目的是研究卵泡发育不同阶段B - M - P受体1B (B - M - PR1b)、FSH R和L - H R的时空蛋白表达。虽然所有受体都定位于卵泡颗粒细胞膜,但时间表达不同。B - M - PR1b在所有卵泡阶段均有表达,FSH R在初级卵泡中均有检测到,hl R在初级和初级卵泡中均不存在,但在后期出现。基于荧光信号强度的定量分析显示,随着卵泡的发育,bm PR1b、FSH R和lh R的表达显著升高(p< 0.001 p< 0.0001 p< 0.0001)。我们得出的结论是,灵敏的免疫荧光标记和计算机三维图像分析的结合证明了原位检测和定量复杂组织结构中少量蛋白质表达的有效工具。
Three-Dimensional Image Analysis to Quantify the Temporo-Spacial Expression of Cellular Receptors
� Abstract≤O varian folliculogenesis is primarily controlled by the action of gonadotropins namely follicle stimulating hormone (FSH) and luteinizing hormone (L H). Several reports indicated that the process of initial recruitment of primordial follicles to the growing follicles is not gonadotropin-dependent but Bone morphogenetic protein (B M P)-dependent. However, this has not been unequivocally confirmed. T he aim of this study was to investigate the temporo-spacial protein expression of the B M P receptors 1B (B M PR1b), FSH R and L H R in several stages of follicle development. W hile the localization of all receptors was found in granulosa cell membrane of the follicles the temporal expression was varied. B M PR1b was expressed in all follicle stages, FSH R was detected in primary follicles onward and L H R was absent in both primordial and primary follicles but appeared in later stages. Q uantitative analysis based on the intensity of fluorescent signals showed that the expression of B M PR1b, FSH R and L H R significantly (p< 0.001 p< 0.0001 p< 0.0001 respectively) increased with follicular development. W e have concluded that the combination of sensitive immunofluorescence labeling and computerized 3D image analysis proves efficient tools for in situ detection and quantification of the expression of small amount of protein in a complex tissue structure.