BMC Developmental Biology最新文献

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Keratin 86 is up-regulated in the uterus during implantation, induced by oestradiol. 角蛋白86在着床期间在子宫中上调,由雌二醇诱导。
BMC Developmental Biology Pub Date : 2020-02-07 DOI: 10.1186/s12861-020-0208-6
He Zhang, Huashan Zhao, Xi Wang, Xiaolin Cui, Lingling Jin
{"title":"Keratin 86 is up-regulated in the uterus during implantation, induced by oestradiol.","authors":"He Zhang,&nbsp;Huashan Zhao,&nbsp;Xi Wang,&nbsp;Xiaolin Cui,&nbsp;Lingling Jin","doi":"10.1186/s12861-020-0208-6","DOIUrl":"https://doi.org/10.1186/s12861-020-0208-6","url":null,"abstract":"<p><strong>Background: </strong>Uterine receptivity is one of the determinants of embryo implantation, which is responsible for pregnancy success. Aberrant embryo implantation due to disrupted uterine receptivity is usually found in ovarian hyperstimulation induced hyperoestrogen patients.</p><p><strong>Results: </strong>This study identified keratin 86 (KRT86), a fibrous structural protein, which was upregulated in uterine endometrium during peri-implantation. Using a hyperoestrogen mouse model established in a previous study, we found abnormal oestradiol (E2) levels during pre-implantation could trigger high expression of Krt86 in the uterine epithelium. In an ovariectomised mouse model, combining oestrogen receptors ERα and ERβ knockout mice models, uterine Krt86 was found to be up-regulated after E2 treatment, mediated by nuclear ERα. Furthermore, we found progesterone (P4) could ameliorate Krt86 expression, induced by abnormal E2.</p><p><strong>Conclusions: </strong>These results revealed the dynamic expression and regulation of Krt86, especially in hyperoestrogen treated mice, indicating it might act as a marker for non-receptive uterus.</p>","PeriodicalId":9130,"journal":{"name":"BMC Developmental Biology","volume":"20 1","pages":"3"},"PeriodicalIF":0.0,"publicationDate":"2020-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12861-020-0208-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37617893","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Downregulation of lncRNA DANCR promotes osteogenic differentiation of periodontal ligament stem cells. lncRNA DANCR下调促进牙周韧带干细胞成骨分化。
BMC Developmental Biology Pub Date : 2020-01-14 DOI: 10.1186/s12861-019-0206-8
Zhuo Wang, Yuanliang Huang, Luanjun Tan
{"title":"Downregulation of lncRNA DANCR promotes osteogenic differentiation of periodontal ligament stem cells.","authors":"Zhuo Wang,&nbsp;Yuanliang Huang,&nbsp;Luanjun Tan","doi":"10.1186/s12861-019-0206-8","DOIUrl":"https://doi.org/10.1186/s12861-019-0206-8","url":null,"abstract":"<p><strong>Background: </strong>Long non-coding RNAs (lncRNAs) have been widely known to have an appreciable effect in physiology and pathology. In tooth regeneration, periodontal ligament stem cells (PDLSCs) are regarded as a key effector, whereas, how lncRNA acts in the osteogenic differentiation of PDLSCs have not been completely understood. This study aims to find out the relationship between lncRNA DANCR and the proliferation and osteogenic differentiation of PDLSCs.</p><p><strong>Methods: </strong>Microarray was used to observe the different expression of lncRNAs in differentiated and undifferentiated PDLSCs. And then osteogenic-related lncRNA, DANCR was screened out. Its effects on proliferation and osteogenic differentiation was explored by constructing an overexpression and inhibition model. qRT-PCR was used to detect the mRNA expression of osteogenesis related genes. MTT assay was performed to assess the effects of DANCR on cell growth curve. To quantify the effects of DANCR on osteogenic differentiation of PDLSCs, ALP staining and alizarin red was performed in basic culture medium and osteogenic medium. Data were statistically processed.</p><p><strong>Results: </strong>Compared with the undifferentiated PDLSCs, the alizarin red staining level was higher in differentiated PDLSCs. And the expressions of osteogenic differentiation marker genes Runt-related transcription factor 2 (Runx2), osteocalcin (OCN) and bone morphogenetic protein (BMP-2) were significantly increased in the differentiated PDLSCs. Furthermore, we noticed that comparing with control groups, the expression of lncRNA DANCR decreases markedly in osteogenically induced PDLSCs. DANCR promoted proliferation of PDLSCs, as evidenced by cell viability. Further investigation has proven that the downregulation of DANCR shows in the calcium sediment forming, alkaline phosphatase (ALP) activation and some osteogenic-related gene markers' upregulation including Runx2, OCN and BMP-2, which finally results in the osteogenic differentiation of PDLSCs following the transfection and induction. Conversely, DANCR upregulation was shown to repress the osteogenic differentiation potential of PDLSCs.</p><p><strong>Conclusions: </strong>The osteogenic differentiation of PDLSCs has proven to related to the down regulation of lncRNA DANCR. And this paper throws light on the effects of DANCR in the process of PDLSCs' osteogenic differentiation.</p>","PeriodicalId":9130,"journal":{"name":"BMC Developmental Biology","volume":"20 1","pages":"2"},"PeriodicalIF":0.0,"publicationDate":"2020-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12861-019-0206-8","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37538223","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 17
Spontaneous embryo resorption in the mouse is triggered by embryonic apoptosis followed by rapid removal via maternal sterile purulent inflammation. 小鼠的自发胚胎吸收是由胚胎凋亡触发的,随后通过母体无菌化脓性炎症快速清除。
BMC Developmental Biology Pub Date : 2020-01-09 DOI: 10.1186/s12861-019-0201-0
Barbara Drews, Luis Flores Landaverde, Anja Kühl, Ulrich Drews
{"title":"Spontaneous embryo resorption in the mouse is triggered by embryonic apoptosis followed by rapid removal via maternal sterile purulent inflammation.","authors":"Barbara Drews,&nbsp;Luis Flores Landaverde,&nbsp;Anja Kühl,&nbsp;Ulrich Drews","doi":"10.1186/s12861-019-0201-0","DOIUrl":"https://doi.org/10.1186/s12861-019-0201-0","url":null,"abstract":"<p><strong>Background: </strong>In normal mammalian development a high percentage of implantations is lost by spontaneous resorption. This is a major problem in assisted reproduction and blastocyst transfer. Which embryo will be resorbed is unpredictable. Resorption is very fast, so that with conventional methods only final haemorrhagic stages are encountered. Here we describe the histology and immunohistochemistry of 23 spontaneous embryo resorptions between days 7 and 13 of murine development, which were identified by high-resolution ultrasound (US) in a previous study.</p><p><strong>Results: </strong>In the early resorptions detected at day 7, the embryo proper was replaced by maternal haemorrhage and a suppurate focus of maternal neutrophils. In the decidua maternal macrophages transformed to foam cells and formed a second focus of tissue dissolution. In the late resorptions detected at day 9, the embryo underwent apoptosis without involvement of maternal cells. The apoptotic embryonic cells expressed caspase 3 and embryonic blood cells developed a macrophage like phenotype. Subsequently, the wall of the embryonic vesicle ruptured and the apoptotic embryo was aborted into the uterine lumen. Abortion was initiated by degeneration of the embryonic lacunar trophoblast and dissolution of the maternal decidua capsularis via sterile inflammation and accompanied by maternal haemorrhage, invasion of the apoptotic embryo by maternal neutrophils, and contraction rings of the uterine muscle layers.</p><p><strong>Conclusions: </strong>We conclude that spontaneous resorption starts with endogenous apoptosis of the embryo without maternal contribution. After break down of the foetal-maternal border, the apoptotic embryo is invaded by maternal neutrophils, aborted into the uterine lumen, and rapidly resorbed. We assume that the innate maternal unspecific inflammation is elicited by disintegrating apoptotic embryonic cells.</p>","PeriodicalId":9130,"journal":{"name":"BMC Developmental Biology","volume":"20 1","pages":"1"},"PeriodicalIF":0.0,"publicationDate":"2020-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12861-019-0201-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37525843","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 17
Expression analysis of Rab11 during zebrafish embryonic development. 斑马鱼胚胎发育过程中Rab11的表达分析。
BMC Developmental Biology Pub Date : 2019-12-30 DOI: 10.1186/s12861-019-0207-7
Haijun Zhang, Yu Gao, Peipei Qian, Zhangji Dong, Wenjin Hao, Dong Liu, Xuchu Duan
{"title":"Expression analysis of Rab11 during zebrafish embryonic development.","authors":"Haijun Zhang,&nbsp;Yu Gao,&nbsp;Peipei Qian,&nbsp;Zhangji Dong,&nbsp;Wenjin Hao,&nbsp;Dong Liu,&nbsp;Xuchu Duan","doi":"10.1186/s12861-019-0207-7","DOIUrl":"https://doi.org/10.1186/s12861-019-0207-7","url":null,"abstract":"<p><strong>Background: </strong>Rab proteins are GTPases responsible for intracellular vesicular trafficking regulation. Rab11 proteins, members of the Rab GTPase family, are known to regulate vesicular recycling during embryonic development. In zebrafish, there are 3 rab11 paralogues, known as rab11a, rab11ba and rab11bb, sharing high identity with each other. However, the expression analysis of rab11 is so far lacking.</p><p><strong>Results: </strong>Here, by phylogeny analysis, we found the three rab11 genes are highly conserved especially for their GTPase domains. We examined the expression patterns of rab11a, rab11ba and rab11bb using RT-PCR and in situ hybridization. We found that all the three genes were highly enriched in the central nervous system, but in different areas of the brain. Apart from brain, rab11a was also expressed in caudal vein, pronephric duct, proctodeum, pharyngeal arches and digestive duct, rab11ba was detected to express in muscle, and rab11bb was expressed in kidney, fin and spinal cord. Different from rab11a and rab11ba, which both have maternal expressions in embryos, rab11bb only expresses during 24hpf to 96hpf.</p><p><strong>Conclusions: </strong>Our results suggest that rab11 genes play important but distinct roles in the development of the nervous system in zebrafish. The findings could provide new evidences for better understanding the functions of rab11 in the development of zebrafish embryos.</p>","PeriodicalId":9130,"journal":{"name":"BMC Developmental Biology","volume":"19 1","pages":"25"},"PeriodicalIF":0.0,"publicationDate":"2019-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12861-019-0207-7","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37497143","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Comparison of the transcriptomes of two tardigrades with different hatching coordination. 两种不同孵化配合的缓步动物转录组的比较。
BMC Developmental Biology Pub Date : 2019-12-09 DOI: 10.1186/s12861-019-0205-9
Yuki Yoshida, Kenta Sugiura, Masaru Tomita, Midori Matsumoto, Kazuharu Arakawa
{"title":"Comparison of the transcriptomes of two tardigrades with different hatching coordination.","authors":"Yuki Yoshida,&nbsp;Kenta Sugiura,&nbsp;Masaru Tomita,&nbsp;Midori Matsumoto,&nbsp;Kazuharu Arakawa","doi":"10.1186/s12861-019-0205-9","DOIUrl":"10.1186/s12861-019-0205-9","url":null,"abstract":"<p><strong>Background: </strong>Tardigrades are microscopic organisms, famous for their tolerance against extreme environments. The establishment of rearing systems of multiple species has allowed for comparison of tardigrade physiology, in particular in embryogenesis. Interestingly, in-lab cultures of limnic species showed smaller variation in hatching timing than terrestrial species, suggesting a hatching regulation mechanism acquired by adaptation to their habitat.</p><p><strong>Results: </strong>To this end, we screened for coordinated gene expression during the development of two species of tardigrades, Hypsibius exemplaris and Ramazzottius varieornatus, and observed induction of the arthropod molting pathway. Exposure of ecdysteroids and juvenile hormone analog affected egg hatching but not embryonic development in only the limnic H. exemplaris.</p><p><strong>Conclusion: </strong>These observations suggest a hatching regulation mechanism by the molting pathway in H. exemplaris.</p>","PeriodicalId":9130,"journal":{"name":"BMC Developmental Biology","volume":"19 1","pages":"24"},"PeriodicalIF":0.0,"publicationDate":"2019-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12861-019-0205-9","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37480868","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 11
Electrochemical gradients are involved in regulating cytoskeletal patterns during epithelial morphogenesis in the Drosophila ovary 电化学梯度参与调节果蝇卵巢上皮形态发生过程中的细胞骨架模式
BMC Developmental Biology Pub Date : 2019-11-12 DOI: 10.1186/s12861-019-0203-y
I. Weiß, J. Bohrmann
{"title":"Electrochemical gradients are involved in regulating cytoskeletal patterns during epithelial morphogenesis in the Drosophila ovary","authors":"I. Weiß, J. Bohrmann","doi":"10.1186/s12861-019-0203-y","DOIUrl":"https://doi.org/10.1186/s12861-019-0203-y","url":null,"abstract":"","PeriodicalId":9130,"journal":{"name":"BMC Developmental Biology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12861-019-0203-y","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48668596","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
Survival of Polyploid hybrid salamander embryos 多倍体杂交蝾螈胚胎的存活
BMC Developmental Biology Pub Date : 2019-11-12 DOI: 10.1186/s12861-019-0202-z
N. Charney, Jacob E. Kubel, C. Woodard, Blanca I. Carbajal-González, Samantha Avis, Julia A. Blyth, Charles S. Eiseman, John J. Castorino, J. Malone
{"title":"Survival of Polyploid hybrid salamander embryos","authors":"N. Charney, Jacob E. Kubel, C. Woodard, Blanca I. Carbajal-González, Samantha Avis, Julia A. Blyth, Charles S. Eiseman, John J. Castorino, J. Malone","doi":"10.1186/s12861-019-0202-z","DOIUrl":"https://doi.org/10.1186/s12861-019-0202-z","url":null,"abstract":"","PeriodicalId":9130,"journal":{"name":"BMC Developmental Biology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12861-019-0202-z","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45801267","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
YWHA (14-3-3) protein isoforms and their interactions with CDC25B phosphatase in mouse oogenesis and oocyte maturation YWHA(14-3-3)蛋白异构体及其与CDC25B磷酸酶在小鼠卵发生和卵母细胞成熟中的相互作用
BMC Developmental Biology Pub Date : 2019-10-22 DOI: 10.1186/s12861-019-0200-1
Alaa A. Eisa, Santanu De, Ariana C. Detwiler, Eva Gilker, Alex Ignatious, S. Vijayaraghavan, D. Kline
{"title":"YWHA (14-3-3) protein isoforms and their interactions with CDC25B phosphatase in mouse oogenesis and oocyte maturation","authors":"Alaa A. Eisa, Santanu De, Ariana C. Detwiler, Eva Gilker, Alex Ignatious, S. Vijayaraghavan, D. Kline","doi":"10.1186/s12861-019-0200-1","DOIUrl":"https://doi.org/10.1186/s12861-019-0200-1","url":null,"abstract":"","PeriodicalId":9130,"journal":{"name":"BMC Developmental Biology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12861-019-0200-1","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45604181","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 20
A modifier in the 129S2/SvPasCrl genome is responsible for the viability of Notch1[12f/12f] mice 129S2/SvPasCrl基因组中的一个修饰子负责Notch1[12f/12f]小鼠的生存能力
BMC Developmental Biology Pub Date : 2019-10-07 DOI: 10.1186/s12861-019-0199-3
Shweta Varshney, Hua-Xing Wei, F. Batista, Mohd Nauman, S. Sundaram, K. Siminovitch, A. Tanwar, P. Stanley
{"title":"A modifier in the 129S2/SvPasCrl genome is responsible for the viability of Notch1[12f/12f] mice","authors":"Shweta Varshney, Hua-Xing Wei, F. Batista, Mohd Nauman, S. Sundaram, K. Siminovitch, A. Tanwar, P. Stanley","doi":"10.1186/s12861-019-0199-3","DOIUrl":"https://doi.org/10.1186/s12861-019-0199-3","url":null,"abstract":"","PeriodicalId":9130,"journal":{"name":"BMC Developmental Biology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12861-019-0199-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41524673","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 17
Sonic hedgehog promotes chondrogenesis of rabbit bone marrow stem cells in a rotary cell culture system 声波刺猬在旋转细胞培养系统中促进兔骨髓干细胞软骨形成
BMC Developmental Biology Pub Date : 2019-08-12 DOI: 10.1186/s12861-019-0198-4
Liyang Chen, Gejun Liu, Wenjun Li, Xing Wu
{"title":"Sonic hedgehog promotes chondrogenesis of rabbit bone marrow stem cells in a rotary cell culture system","authors":"Liyang Chen, Gejun Liu, Wenjun Li, Xing Wu","doi":"10.1186/s12861-019-0198-4","DOIUrl":"https://doi.org/10.1186/s12861-019-0198-4","url":null,"abstract":"","PeriodicalId":9130,"journal":{"name":"BMC Developmental Biology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12861-019-0198-4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45990877","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
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