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1.
Biol Reprod ; 111(1): 135-147, 2024 Jul 12.
Artículo en Inglés | MEDLINE | ID: mdl-38401166

RESUMEN

OBJECTIVE: This study aimed to explore the specific pathways by which HOX transcript antisense intergenic RNA contributes to the pathogenesis of unexplained recurrent spontaneous abortion. METHODS: Real-time quantitative PCR was employed to assess the differential expression levels of HOX transcript antisense intergenic RNA in chorionic villi tissues from unexplained recurrent spontaneous abortion patients and women with voluntarily terminated pregnancies. HTR-8/SVneo served as a cellular model. Knockdown and overexpression of HOX transcript antisense intergenic RNA in the cells were achieved through siRNA transfection and pcDNA3.1 transfection, respectively. Cell viability, migration, and invasion were evaluated using cell counting kit-8, scratch, and Transwell assays, respectively. The interaction among the HOX transcript antisense intergenic RNA /miR-1277-5p/fibrillin 2 axis was predicted through bioinformatics analysis and confirmed through in vitro experiments. Furthermore, the regulatory effects of the HOX transcript antisense intergenic RNA /miR-1277-5p/fibrillin 2 signaling axis on cellular behaviors were validated in HTR-8/SVneo cells. RESULTS: We found that HOX transcript antisense intergenic RNA was downregulated in chorionic villi tissues from unexplained recurrent spontaneous abortion patients. Overexpression of HOX transcript antisense intergenic RNA significantly enhanced the viability, migration, and invasion of HTR-8/SVneo cells, while knockdown of HOX transcript antisense intergenic RNA had the opposite effects. We further confirmed the regulatory effect of the HOX transcript antisense intergenic RNA /miR-1277-5p/fibrillin 2 signaling axis in unexplained recurrent spontaneous abortion. Specifically, HOX transcript antisense intergenic RNA and fibrillin 2 were found to reduce the risk of unexplained recurrent spontaneous abortion by enhancing cell viability, migration, and invasion, whereas miR-1277-5p exerted the opposite effects. CONCLUSION: HOX transcript antisense intergenic RNA promotes unexplained recurrent spontaneous abortion development by targeting inhibition of miR-1277-5p/fibrillin 2 axis.


Asunto(s)
Aborto Habitual , Movimiento Celular , MicroARNs , ARN Largo no Codificante , Transducción de Señal , Humanos , MicroARNs/genética , MicroARNs/metabolismo , Femenino , Aborto Habitual/genética , Aborto Habitual/metabolismo , Aborto Habitual/patología , ARN Largo no Codificante/genética , ARN Largo no Codificante/metabolismo , Embarazo , Fibrilina-2/genética , Fibrilina-2/metabolismo , Adulto , Proliferación Celular , Línea Celular , Trofoblastos/metabolismo , Trofoblastos/fisiología , Vellosidades Coriónicas/metabolismo
2.
J Dent Sci ; 15(1): 114-117, 2020 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-32257011

RESUMEN

To evaluate the association between congenital missing of maxillary lateral incisor (MLI) with cervical vertebral body fusions, posterior arch deficiency, and both anomalies. A total of 64 subjects (24 males and 40 females; mean age 16 ± 4.5 years) were detected to have congenital missing of MLI and selected as a study group. Two hundred and fifty-six subjects (87 males and 169 females, mean age 18.1 ± 3.2 years) were assigned to the control group. In the congenital absence of MLI, 53.7% revealed cervical column body fusion, 11.1% indicated a posterior arch deficiency, and 9.3% showed cervical column body fusion with posterior arch deficiency. Morphological deviations of the cervical column showed significant associations with congenital absence of MLI compared to control group (p < 0.001). There were no significant differences in gender among the study and control groups (p > 0.05). Subjects with congenial MLI tend to have an increased frequency of cervical anomaly.

3.
Shanghai Kou Qiang Yi Xue ; 26(1): 69-72, 2017 Feb.
Artículo en Zh | MEDLINE | ID: mdl-28474070

RESUMEN

PURPOSE: Based on the research of the congenital missing of the third molar and the missing number, the relationship beteen congenital missing of the third molar and the development of the mandibular angle was evaluated. METHODS: Patients were divided into experimental group and control group, the experimental group included 227 patients, each had at least one of the third molars congenital lost; 227 patients who had four third molar were selected as control group. Winceph software was used to measure the lateral cephalograms. SPSS17.0 software package was used to perform statistical analysis. RESULTS: Gonial angle, upper Gonial angle and lower Gonial angle between the experimental group and the control group showed significant difference and the values in the experimental group were significantly smaller than in the control group, but there was no gender difference between the two groups.There was no difference between Gonial angle, upper Gonial angle,lower Gonial angle and the missing number of the third molar. CONCLUSIONS: There is a close relationship between congenital missing third molar and Gonial angle, upper Gonial angle, lower Gonial angle, but there is no significant association with gender and the patients with congenital missing third molar have shorter craniofacial structure. Congenital missing number of the third molar has no significant association with Gonial angle, upper Gonial angle and lower Gonial angle.


Asunto(s)
Anodoncia , Mandíbula/fisiología , Tercer Molar , Femenino , Humanos , Masculino
4.
Shanghai Kou Qiang Yi Xue ; 26(1): 73-75, 2017 Feb.
Artículo en Zh | MEDLINE | ID: mdl-28474071

RESUMEN

PURPOSE: To investigate the association between palatally displaced canines and cervical skeletal abnormalities by lateral cephalometric, panoramic radiographs and cone-beam CT. METHODS: One hundred and three patients with palatally displaced canines were chosen as the experimental group, and 103 patients with Class I and normal canines eruption were as the control group.The data of the first four cervical fusions and posterior arch defects were measured on the lateral cephalometrics. The relationship of the cervical skeletal abnormalities and palatally displaced canines was analyzed with SPSS 21.0 software package for Chi-square test. RESULTS: The incidence of cervical fusion in the experimental group was 71.84%(74 cases), while 15.53% (16 cases) in the control group; the difference between the experimental group and the control group was significant (P<0.001); the incidence of posterior arch defects in the experimental group was 10.68% (11 cases) and 4.85%(5 cases) in the control group; the difference between the experimental group and the control group was not significant. CONCLUSIONS: There is an obviously increasing occurrence rate of cervical skeletal abnormalities in patients with palatally displaced canines, and cervical vertebra bone abnormalities can be combined with other diagnostic parameters to confirm the situation of impacted canines.


Asunto(s)
Cefalometría , Diente Canino/anomalías , Maxilar/anomalías , Radiografía Panorámica , Adolescente , Niño , Tomografía Computarizada de Haz Cónico , Femenino , Humanos , Masculino , Erupción Dental , Diente Impactado
5.
Protein Sci ; 26(4): 834-846, 2017 04.
Artículo en Inglés | MEDLINE | ID: mdl-28168758

RESUMEN

TBC1D15 belongs to the TBC (Tre-2/Bub2/Cdc16) domain family and functions as a GTPase-activating protein (GAP) for Rab GTPases. So far, the structure of TBC1D15 or the TBC1D15·Rab complex has not been determined, thus, its catalytic mechanism on Rab GTPases is still unclear. In this study, we solved the crystal structures of the Shark and Sus TBC1D15 GAP domains, to 2.8 Å and 2.5 Å resolution, respectively. Shark-TBC1D15 and Sus-TBC1D15 belong to the same subfamily of TBC domain-containing proteins, and their GAP-domain structures are highly similar. This demonstrates the evolutionary conservation of the TBC1D15 protein family. Meanwhile, the newly determined crystal structures display new variations compared to the structures of yeast Gyp1p Rab GAP domain and TBC1D1. GAP assays show that Shark and Sus GAPs both have higher catalytic activity on Rab11a·GTP than Rab7a·GTP, which differs from the previous study. We also demonstrated the importance of arginine and glutamine on the catalytic sites of Shark GAP and Sus GAP. When arginine and glutamine are changed to alanine or lysine, the activities of Shark GAP and Sus GAP are lost.


Asunto(s)
Proteínas de Peces/química , Proteínas Activadoras de GTPasa/química , Guanosina Trifosfato/química , Complejos Multiproteicos/química , Proteínas de Unión al GTP rab/química , Animales , Cristalografía por Rayos X , Proteínas de Peces/metabolismo , Proteínas Activadoras de GTPasa/metabolismo , Guanosina Trifosfato/metabolismo , Humanos , Complejos Multiproteicos/metabolismo , Estructura Cuaternaria de Proteína , Tiburones , Porcinos , Proteínas de Unión al GTP rab/metabolismo
6.
ACS Appl Mater Interfaces ; 8(48): 32948-32955, 2016 Dec 07.
Artículo en Inglés | MEDLINE | ID: mdl-27934147

RESUMEN

In this work, epitaxial Pb(Zr0.4Ti0.6)O3 (PZT) thin films with different thicknesses were deposited on Nb-doped SrTiO3 (NSTO) single-crystal substrates by chemical solution deposition (CSD), and their ferroelectric resistive switching behaviors were investigated. The results showed that the maximum ON/OFF ratio up to 850 could be obtained in the PZT/NSTO heterostructure with the 150 nm thick PZT film. On the basis of the Schottky-Simmons model and the modified semiconductor theory, we also evaluated the interfacial built-in field and the depletion layer at the PZT/NSTO interface, which can be modulated strongly by the ferroelectric polarization, but are independent of the thickness of the PZT thin films. It is clear that the ferroelectric resistive switching is related to the ferroelectric polarization and modulated by the thickness of ferroelectric films. Therefore, there is an optimal thickness of the PZT film for the maximum ON/OFF ratio due to the ferroelectricity and conductivity mutually restricting. It can be expected that by adjusting the ferroelectricity and conductivity of the ferroelectric thin film and its thickness, the maximum switching ratio can be further improved.

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