1.Spatial expression of cardiac alpha-actin during heart development in embryos.
Fang LIU ; Shu-bao CHEN ; Xiao-qing LIU ; Wen-zhu ZHANG
Chinese Journal of Pediatrics 2005;43(10):772-776
OBJECTIVEConotruncal defects (CTD) is a common type of cyanotic congenital heart defects. It was shown that CTD might be produced by ablation of cardiac neural crest during early stage embryos in experimental studies. There were many kinds of genes involved and cardiac alpha-actin (CAA) was one of them. The purpose of this study was to investigate the spatial expression of CAA gene during embryonic heart development, and to explore its role in the pathogenesis of congenital heart defects.
METHODSExperimental chicken embryos were subjected to cardiac neural crest ablation by using electric stimulation at 36-40 hr incubation stage. The embryos and organs of experimental and normal control groups during different developing periods were taken out, RNA was extracted by Trizol, and then reverse transcription was done. The dynamic changes of CAA mRNA expression at different development stages of embryos were assayed by fluorescent real-time PCR. The embryos and tissues at different stages were taken out, and paraffin sections were made. The localizations of CAA antibody expression in the developmental embryos were detected by immunohistochemical analysis (peroxidase-DAB coloration).
RESULTS(1) The expression of CAA gene was detected at early embryo development, and increased subsequently to a stable level. Its expression was mainly limited to heart site, and could be increased along with the maturation of the cardiac muscle. There was no expression or little trace expression in liver, brain, and stomach. (2) There was a significantly low level of CAA gene expression on days 2-7 of chicken embryos whose cardiac neural crest were ablated in comparison with normal controls (P = 0.013). The level of CAA gene expression was also down-regulated on days 7, 9 and 15 of embryonic cardiac tissues (P = 0.029).
CONCLUSIONCAA gene is closely associated with heart development, its expression was adjusted by cardiac neural crest, and its dysfunction may be an important factor leading to congenital heart defects.
Actins ; genetics ; metabolism ; Animals ; Chick Embryo ; Gene Expression Regulation, Developmental ; Heart ; embryology ; Heart Defects, Congenital ; embryology ; Neural Crest ; embryology
2.Distribution and ontogeny of gastrin- and serotonin-immunoreactive cells in the proventriculus of developing chick, Gallus gallus domestica.
Abdulkerim AKSOY ; Kenan CINAR
Journal of Veterinary Science 2009;10(1):9-13
The ontogeny and distribution of gastrin- and serotonin-immunoreactive (IR) cell in the proventriculus of chicks (Gallus gallus domestica, n = 60) in different growth periods was examined immunohistochemically using antisera specific to gastrin and serotonin. Gastrin and serotonin-IR cells were detected in chick proventriculus. Gastrin-IR cells were first evident after 12 days of incubation in lamina epithelialis and compound glands, while serotonin-IR cells were observed only in compound glands at that same time. Gastrin-IR and serotonin-IR cells increased in frequency on incubation day 14 and 16, respectively. Towards the end of incubation, gastrin- and serotonin-IR cell numbers decreased. In adult chicken, both IR cells were present but not lower numbers. The observations demonstrate the presence of gastrin- and serotonin-IR cells in the proventriculus of developing chicks in temporally changing frequencies.
Animals
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Chick Embryo/*metabolism
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Endocrine Cells/cytology/metabolism
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Gastrins/*metabolism
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Gene Expression Regulation, Developmental/physiology
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Proventriculus/*embryology/*metabolism
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Serotonin/*metabolism
3.Expression of Cx43 and Pax3 in the small intestinal muscular layers of early human embryos.
Xue-hong LIU ; Jin-ping ZHANG ; Shu-ying HE ; Weng-fang SONG
Journal of Southern Medical University 2008;28(4):634-636
OBJECTIVETo explore the patterns of Cx43 and Pax3 protein expressions in the small intestinal muscular layers of human embryo during early development.
METHODSImmunohistochemistry with SABC method was employed to examine the expression of Cx43 and Pax3 proteins in the muscular layers of the small intestine in early human embryos in the second to fourth months of gestation.
RESULTSIn the second month of gestation, the muscle layer of the small intestine was negative for Cx43 and Pax3 protein expressions. In the third month, Cx43 and Pax3 expressions were negative in the inner circular muscle layer, but some positive cells were found in the longitudinal muscle layer and the myenteric plexus. In the fourth month, positive expression of Cx43 and Pax3 proteins were seen in the entire muscle layer.
CONCLUSIONCx43 and Pax3 proteins are closely related to the growth and development of the cells and tissues in the small intestinal muscle layer in human embryos.
Connexin 43 ; biosynthesis ; Embryo, Mammalian ; metabolism ; Humans ; Immunohistochemistry ; Intestine, Small ; embryology ; metabolism ; Muscle, Smooth ; embryology ; metabolism ; PAX3 Transcription Factor ; Paired Box Transcription Factors ; biosynthesis
4.Biallelic mutations in CDC20 cause female infertility characterized by abnormalities in oocyte maturation and early embryonic development.
Lin ZHAO ; Songguo XUE ; Zhongyuan YAO ; Juanzi SHI ; Biaobang CHEN ; Ling WU ; Lihua SUN ; Yao XU ; Zheng YAN ; Bin LI ; Xiaoyan MAO ; Jing FU ; Zhihua ZHANG ; Jian MU ; Wenjing WANG ; Jing DU ; Shuai LIU ; Jie DONG ; Weijie WANG ; Qiaoli LI ; Lin HE ; Li JIN ; Xiaozhen LIANG ; Yanping KUANG ; Xiaoxi SUN ; Lei WANG ; Qing SANG
Protein & Cell 2020;11(12):921-927
5.Expression of TGFbeta Family in the Developing Internal Ear of Rat Embryos.
Ho Jeong KIM ; Ki Young KANG ; Jin Ghi BAEK ; Hyoung Chul JO ; Hyun KIM
Journal of Korean Medical Science 2006;21(1):136-142
In order to investigate the expression patterns of the transforming growth factor (TGF)beta isoforms in the internal ear, an immunohistochemical study of rat embryos was performed. Rat embryos were taken on the 13th, 15th, 17th, and 19th day after conception and their internal ears were immunohistochemically stained against TGF beta1, beta2, and beta3. As a result, the 13-day-old embryo showed a very weak positivity to TGF beta1. After the 15th day of pregnancy, no reactivity to TGF beta1 was defected. Immunoreactivity to TGF beta2 was observed from the 15th day of pregnancy throughout the rest of the period. The ampulla of the semicircular canal and the cochlear duct showed a notably strong immunohistochemical reaction. A strong reaction to TGF beta3 was observed on the 15th day of pregnancy. However, no positive reactions were observed thereafter. A strong immunoreactivity was observed especially on the apical cytoplasms, the surfaces of the epithelial cells, and basement membranes of the cochlear duct, as well as the semicircular canals of the developing internal ear of rat embryo.
Animals
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Ear, Inner/embryology/*metabolism
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Embryo/embryology/*metabolism
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Female
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Immunohistochemistry
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Male
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Rats
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Rats, Sprague-Dawley
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Time Factors
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Transforming Growth Factor beta/*biosynthesis
6.Immunoreactivity of Constitutive and Inducible Heat Shock Protein 70 in Human Fetal Retina.
Jeong Hun KIM ; Young Suk YU ; Jin Hyoung KIM ; Yu Jeong KIM ; Jang Won HEO ; Chong Jai KIM
Korean Journal of Ophthalmology 2003;17(1):14-18
The purpose of this study was to measure the level of expression of the inducible heat shock protein70 (Hsp70), the constitutive heat shock protein70 (Hsc70) in the outer nuclear layer and the photoreceptors in the human fetal retina. Fetal eyeballs were selected from fetal autopsy specimens of 12 and 17 to 40 week old fetuses, with no history of congenital anomalies. The retinas had differentiated from neuroblastic cells, into matured sensory retinas, from a gestational age (GA) from 12 to 36 weeks. The Hsp70 and Hsc70 were prominently expressed in the nuclear layers. The Hsc70 was expressed at all GAs and the Hsp70 was expressed from 20 to 33 weeks GA. This period is in accordance with the maturation of the sensory retina. The expression of heat shock protein may be regulated by the development of the fetus, and play an important role in the ocular development.
Embryo and Fetal Development
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Fetus/metabolism
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Heat-Shock Proteins 70/*metabolism
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Human
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Immunohistochemistry
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Retina/*embryology
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Support, Non-U.S. Gov't
7.Positional cloning of a novel allele of zebrafish cloche mutant.
Ning MA ; Zhong-jun HUO ; Guang YAN ; Hong-hui HUANG ; Shen-qiu LUO ; Wen-qing ZHANG
Journal of Southern Medical University 2010;30(3):458-462
OBJECTIVETo perform the genetic identification of cloche(172) mutant zebrafish.
METHODSThe chemical mutagen N-ethyl-N-nitrosourea (ENU) was used to treat the AB stain male fish. Large-scale forward genetic screening was carried out to search for lyC-deficient zebrafish mutant by WISH. The morphology changes of the embryos at 3 days postfertilization (3dpf) stage were observed and the cloche(172) gene was identified by mapping and complementation test.
RESULTSWe selected 4 lyC-deficient zebrafish by WISH. cloche(172) mutant showed morphological changes similar to cloche mutant in 3dpf stage. One fourth of the embryos showed cloche phenotype as found in complementation test, and the cloche(172) gene was mapped on the telomere of zebrafish 13 chromosome where cloche gene was located. Numerous red blood cells were observed in the cloche(172) mutant, while only a few cells were found in the cloche mutant in the tail region by o-dianisdine staining.
CONCLUSIONcloche(172) gene which is responsible for the phenotype of cloche mutant may be a novel point mutation allele of the cloche mutant.
Alleles ; Animals ; Chromosome Mapping ; Cloning, Molecular ; Embryo, Nonmammalian ; embryology ; metabolism ; Ethylnitrosourea ; toxicity ; Genetic Complementation Test ; Male ; Muramidase ; genetics ; Mutation ; Zebrafish ; embryology ; genetics ; Zebrafish Proteins ; genetics
8.Retinoic acid signal pathway regulation of zebra fish tooth development through manipulation of the differentiation of neural crest.
Xin LIU ; Xing HUANG ; Zhiyun XU ; Deqin YANG
West China Journal of Stomatology 2016;34(2):115-120
OBJECTIVETo investigate the mechanism of retinoic acid (RA) signal in dental evolution, RA is used to explore the influence of the mechanism on neural crest's migration during the early stage of zebra fish embryos.
METHODSWe divided embryos of wild type and transgenic line zebra fish into three groups. 1 x 10(-7) to 6 x 10(-7) mol x L(-1) RA and 1 x 10(-7) mo x L(-1) 4-diethylaminobenzaldehyde (DEAB) were added into egg water at 24 hpf for 9 h. Dimethyl sulfoxid (DMSO) with the concentration was used as control group. Then, antisense probes of dlx2a, dlx2b, and barxl were formulated to perform whole-mount in situ hybridization to check the expressions of the genes in 48 hpf to 72 hpf embryos. We observed fluorescence of transgenic line in 4 dpf embryos.
RESULTSWe obtained three mRNA probes successfully. Compared with DMSO control group, a low concentration (1 x 10(-7) mol x L(-1)) of RA could up-regulate the expression of mRNA (barx1, dlx2a) in neural crest. Obvious migration trend was observed toward the pharyngeal arch in which teeth adhered. Transgenic fish had spreading fluorescence tendency in pharyngeal arch. However, a high concentration (4 x 10(-7) mol x L(-1)) of RA malformed the embryos and killed them after treatment. One third of the embryos of middle concentration (3 x 10(-7) mo x L(-1)) exhibited delayed development. DEAB resulted in neural crest dysplasia. The expression of barxl and dlx2a were suppressed, and the appearance of dlx2b in tooth was delayed.
CONCLUSIONRA signal pathway can regulate the progenitors of tooth by controlling the growth of the neural crest and manipulating tooth development
Animals ; Branchial Region ; Cell Differentiation ; drug effects ; Embryo, Nonmammalian ; drug effects ; embryology ; metabolism ; In Situ Hybridization ; Neural Crest ; drug effects ; Odontogenesis ; Signal Transduction ; Tooth ; drug effects ; embryology ; metabolism ; Tretinoin ; pharmacology ; Zebrafish ; embryology ; genetics ; metabolism
9.Effect of external retinoic acid on Tbx1 gene during zebrafish embryogenesis.
Li-Feng ZHANG ; Yong-Hao GUI ; Tao ZHONG ; Yue-Xiang WANG ; Lin-Xi QIAN ; Yong-Xin DONG ; Qiu JIANG ; Shu-Na SUN ; Hou-Yan SONG
Chinese Journal of Pediatrics 2007;45(4):267-271
OBJECTIVEDiGeorge/del22q11 syndrome is one of the most common genetic causes of outflow tract and aortic arch defects in human. DiGeorge/del22q11 is thought to involve an embryonic defect restricted to the pharyngeal arches and the corresponding pharyngeal pouches. Previous studies have evidenced that retinoic acid (RA) signaling is definitely indispensable for the development of the pharyngeal arches. Tbx1, one of the T-box containing genes, is proved to be the most attractive candidate gene for DiGeorge/del22q11 syndrome. However, the interaction between RA and Tbx1 has not been fully investigated. Exploring the interaction will contribute to discover the molecular pathways disrupted in DiGeorge/del22q11 syndrome, and will also be essential for understanding genetic basis for congenital heart disease. It now seems possible that genes and molecular pathways disrupted in DiGeorge syndrome will also account for some isolated cases of congenital heart disease. Accordingly, the present study aimed to extensively study the effects of external RA on the cardiac development and Tbx1 expression during zebrafish embryogenesis.
METHODSThe chemical genetics approach was applied by treating zebrafish embryos with 5 x 10(-8) mol/L RA and 10(-7) mol/L RA at 12.5 hour post fertilization (hpf). The expression patterns of Tbx1 were monitored by whole-mount in situ hybridization and quantitative real-time RT-PCR, respectively.
RESULTSThe zebrafish embryos treated with 5 x 10(-8) mol/L RA and 10(-7) mol/L RA for 1.5 h at 12.5 hpf exhibited selective defects of abnormal heart tube. The results of whole-mount in situ hybridization with Tbx1 RNA probe showed that Tbx1 was expressed in cardiac region, pharyngeal arches and otic vesicle during zebrafish embryogenesis. RA treatment led to a distinct spatio-temporal expression pattern for Tbx1 from that in wild type embryo. The real-time PCR analysis showed that Tbx1 expression levels were markedly reduced by RA treatment. Tbx1 expression in the pharyngeal arches and heart were obviously down regulated compared to the wild type embryos. In contrast to 5 x 10(-8) mol/L RA-treated groups, 10(-7) mol/L RA caused a more severe effect on the Tbx1 expression level.
CONCLUSIONThese results suggested that there was a genetic link between RA and Tbx1 during development of zebrafish embryo. RA could produce an altered Tbx1 expression pattern in zebrafish. RA may regulate the Tbx1 expression in a dose-dependant manner. RA could represent a major epigenetic factor to cause abnormal expression of Tbx1, secondarily, disrupt the pharyngeal arch and heart development.
Animals ; Branchial Region ; drug effects ; embryology ; Embryo, Nonmammalian ; drug effects ; Embryonic Development ; drug effects ; Gene Expression Regulation, Developmental ; Heart ; drug effects ; embryology ; T-Box Domain Proteins ; genetics ; metabolism ; Tretinoin ; pharmacology ; Zebrafish ; embryology ; genetics ; Zebrafish Proteins ; genetics ; metabolism
10.AKAP12 regulates vascular integrity in zebrafish.
Hyouk Bum KWON ; Yoon Kyung CHOI ; Jhong Jae LIM ; Seung Hae KWON ; Song HER ; Hyun Jin KIM ; Kyung Joon LIM ; Jong Chan AHN ; Young Myeong KIM ; Moon Kyung BAE ; Jeong Ae PARK ; Chul Ho JEONG ; Naoki MOCHIZUKI ; Kyu Won KIM
Experimental & Molecular Medicine 2012;44(3):225-235
The integrity of blood vessels controls vascular permeability and extravasation of blood cells, across the endothelium. Thus, the impairment of endothelial integrity leads to hemorrhage, edema, and inflammatory infiltration. However, the molecular mechanism underlying vascular integrity has not been fully understood. Here, we demonstrate an essential role for A-kinase anchoring protein 12 (AKAP12) in the maintenance of endothelial integrity during vascular development. Zebrafish embryos depleted of akap12 (akap12 morphants) exhibited severe hemorrhages. In vivo time-lapse analyses suggested that disorganized interendothelial cell-cell adhesions in akap12 morphants might be the cause of hemorrhage. To clarify the molecular mechanism by which the cell-cell adhesions are impaired, we examined the cell-cell adhesion molecules and their regulators using cultured endothelial cells. The expression of PAK2, an actin cytoskeletal regulator, and AF6, a connector of intercellular adhesion molecules and actin cytoskeleton, was reduced in AKAP12-depleted cells. Depletion of either PAK2 or AF6 phenocopied AKAP12-depleted cells, suggesting the reduction of PAK2 and AF6 results in the loosening of intercellular junctions. Consistent with this, overexpression of PAK2 and AF6 rescued the abnormal hemorrhage in akap12 morphants. We conclude that AKAP12 is essential for integrity of endothelium by maintaining the expression of PAK2 and AF6 during vascular development.
A Kinase Anchor Proteins/*genetics/metabolism
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Animals
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Blood Vessels/abnormalities/*embryology/metabolism
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Cell Cycle Proteins/genetics/metabolism
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Down-Regulation
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Embryo, Nonmammalian/abnormalities/*blood supply/embryology/metabolism
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Gene Deletion
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*Gene Expression Regulation, Developmental
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Hemorrhage/*embryology/genetics/metabolism
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Human Umbilical Vein Endothelial Cells
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Humans
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Intercellular Junctions/genetics/metabolism/ultrastructure
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Kinesin/genetics/metabolism
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Myosins/genetics/metabolism
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Zebrafish/*embryology/genetics
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p21-Activated Kinases/genetics/metabolism