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羊水细胞的神经起源。

Neural origin of cells in amniotic fluid.

作者信息

Sarkar S, Chang H C, Porreco R P, Jones O W

出版信息

Am J Obstet Gynecol. 1980 Jan 1;136(1):67-72. doi: 10.1016/0002-9378(80)90566-9.

DOI:10.1016/0002-9378(80)90566-9
PMID:7352489
Abstract

Cells from the amniotic fluid of fetuses with open neural tube defects (NTDs) have several abnormal characteristics of potential diagnostic value. The cell number in a unit volume of fluid is 10 to 100 times the normal range of cell count. The majority of cells adhere to tissue culture dishes within 24 hours of inoculation, instead of the 4 or 5 days required by normal amniotic fluid cells. The rapidly adhering cells morphologically resemble glial cells. Their Coulter volume is about twice the average seen in normal amniotic fluid--derived cells. This larger number of oversized, rapidly adhering cells is likely due to the continuous accumulation of neural cells in the amniotic fluid. We have detected the presence of the glial protein S-100 and the absence of the neuronal protein 14-3-2 by using a specific immunofluorescence assay. We conclude that fetuses with NTDs shed large numbers of glialike cells into the amniotic fluid where their detection may have diagnostic importance.

摘要

患有开放性神经管缺陷(NTDs)的胎儿羊水中的细胞具有若干具有潜在诊断价值的异常特征。单位体积羊水中的细胞数量是正常细胞计数范围的10到100倍。大多数细胞在接种后24小时内就附着于组织培养皿,而正常羊水细胞则需要4或5天。快速附着的细胞在形态上类似于神经胶质细胞。它们的库尔特体积约为正常羊水来源细胞平均体积的两倍。这种大量超大、快速附着的细胞可能是由于神经细胞在羊水中持续积累所致。我们通过使用特异性免疫荧光测定法检测到了神经胶质蛋白S-100的存在以及神经元蛋白14-3-2的缺失。我们得出结论,患有NTDs的胎儿会向羊水中释放大量类神经胶质细胞,对其进行检测可能具有诊断意义。

相似文献

1
Neural origin of cells in amniotic fluid.羊水细胞的神经起源。
Am J Obstet Gynecol. 1980 Jan 1;136(1):67-72. doi: 10.1016/0002-9378(80)90566-9.
2
[SEM morphology of rapidly adhering amniotic fluid cells of fetuses with neural tube defects].[神经管缺陷胎儿羊水快速贴壁细胞的扫描电镜形态学]
Pathologica. 1983;75 Suppl:200-3.
3
Demonstration of astrocytes in cultured amniotic fluid cells of three cases with neural-tube defect.三例神经管缺陷患者培养羊水细胞中星形胶质细胞的显示
Hum Genet. 1981;56(3):365-70. doi: 10.1007/BF00274694.
4
[Morphology of rapidly adhering amniotic fluid cells and antenatal diagnosis of neural tube defects].[快速黏附羊水细胞的形态学与神经管缺陷的产前诊断]
Zhonghua Yi Xue Za Zhi. 1982 Sep;62(9):547-9.
5
[Scanning electron-microscopy study of the rapidly adhering cells of amniotic fluid from a fetus with open neural tube defects].[开放性神经管缺陷胎儿羊水快速黏附细胞的扫描电子显微镜研究]
Zhonghua Yi Xue Za Zhi. 1984 Nov;64(11):684-5.
6
Amniotic fluid acetylcholinesterase electrophoresis in the prenatal diagnosis of neural tube defects.羊水乙酰胆碱酯酶电泳在神经管缺陷产前诊断中的应用
S Afr Med J. 1982 Sep 18;62(13):441-2.
7
Morphology of rapidly adhering amniotic-fluid cells as an aid to the diagnosis of neural-tube defects.快速黏附羊水细胞的形态学对神经管缺陷诊断的辅助作用
Lancet. 1977 Apr 30;1(8018):919-22. doi: 10.1016/s0140-6736(77)92221-8.
8
Rapidly adhering amniotic-fluid cells and prenatal diagnosis of neural-tube defects.快速黏附羊水细胞与神经管缺陷的产前诊断
Lancet. 1979 Jul 14;2(8133):99. doi: 10.1016/s0140-6736(79)90150-8.
9
Targeted quantitative amniotic cell profiling: a potential diagnostic tool in the prenatal management of neural tube defects.靶向定量羊膜细胞分析:神经管缺陷产前管理的潜在诊断工具。
J Pediatr Surg. 2013 Jun;48(6):1205-10. doi: 10.1016/j.jpedsurg.2013.03.009.
10
Characterization of rapidly adhering amniotic fluid cells by combined immunofluorescence and phagocytosis assays.通过联合免疫荧光和吞噬作用分析对快速黏附羊水细胞进行表征
Am J Hum Genet. 1989 Nov;45(5):786-92.

引用本文的文献

1
Enhancement of human amniotic cell growth by Ficoll-Paque gradient fractionation.通过Ficoll-Paque密度梯度离心法增强人羊膜细胞生长
In Vitro. 1981 Jan;17(1):81-90. doi: 10.1007/BF02618035.
2
Demonstration of astrocytes in cultured amniotic fluid cells of three cases with neural-tube defect.三例神经管缺陷患者培养羊水细胞中星形胶质细胞的显示
Hum Genet. 1981;56(3):365-70. doi: 10.1007/BF00274694.
3
Glial origin of rapidly adhering amniotic fluid cells.快速黏附羊水细胞的神经胶质起源
Br Med J. 1980 Nov 29;281(6253):1456-7. doi: 10.1136/bmj.281.6253.1456.
4
Cell morphology in long-term cultures of normal and abnormal amniotic fluids.正常和异常羊水长期培养中的细胞形态
Hum Genet. 1982;60(4):310-3. doi: 10.1007/BF00569209.
5
Characterization of rapidly adhering amniotic fluid cells by combined immunofluorescence and phagocytosis assays.通过联合免疫荧光和吞噬作用分析对快速黏附羊水细胞进行表征
Am J Hum Genet. 1989 Nov;45(5):786-92.