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体外损伤腭板的抬高

Elevation of lesioned palatal shelves in vitro.

作者信息

Brinkley L L, Vickerman M M

出版信息

J Embryol Exp Morphol. 1979 Dec;54:229-40.

PMID:528868
Abstract

Fetuses were obtained from CD-1 mice at a time estimated to be 12 h prior to vivo secondary palate closure. One of the palatal shelves of each partially dissected fetal head was lesioned in one of five ways, the other left intact to serve as control. Single transverse cuts extending the width of the shelf were made at one of three positions along the longitudinal axis of the shelf: one-third, one-half or two-thirds the shelf length estimated from the rostral edge. Some specimens were cut in two places, dividing the shelf into three equal segments. Another group received a lesion which separated the caudal third of the shelf from its maxillary connections. All specimens were cultured for 18 h. At the end of the culture period the heads were fixed, examined and the degree of elevation of each shelf piece assessed. Intact, control shelves of all preparations were elevated in the rostral two-thirds of the shelf, while the caudal third was partially elevated. Results seen in lesioned shelves depended upon both the size of the segment and the region of the shelf contained in the segment. The rostral two-thirds of the shelf, the presumptive hard palate, whether intact or in segments elevated without physical connections to neighboring shelf tissue. Thus, it is unlikely that this elevation requires a wave of contraction be transmitted from the caudal soft palate region. In contrast, the presumptive soft palate requires continuity with the rostral portions of the shelf both to maintain structural stability and to elevate.

摘要

在预计体内继发腭闭合前12小时从CD-1小鼠获取胎儿。将每个部分解剖的胎儿头部的一个腭突以五种方式之一进行损伤,另一个保持完整作为对照。在沿着腭突纵轴的三个位置之一进行延伸腭突宽度的单一横向切割:从吻端边缘估计的腭突长度的三分之一、二分之一或三分之二处。一些标本在两个位置进行切割,将腭突分成三个相等的部分。另一组接受的损伤是将腭突的尾端三分之一与其上颌连接分离。所有标本培养18小时。在培养期结束时,将头部固定、检查并评估每个腭突部分的抬高程度。所有标本完整的对照腭突在腭突的吻端三分之二处抬高,而尾端三分之一部分抬高。损伤腭突的结果取决于部分的大小以及该部分所含腭突的区域。腭突的吻端三分之二,即推定的硬腭,无论完整与否或分成几段,都能在没有与相邻腭突组织的物理连接的情况下抬高。因此,这种抬高不太可能需要从尾端软腭区域传递一波收缩。相比之下,推定的软腭需要与腭突的吻端部分保持连续性,以维持结构稳定性并实现抬高。

相似文献

1
Elevation of lesioned palatal shelves in vitro.体外损伤腭板的抬高
J Embryol Exp Morphol. 1979 Dec;54:229-40.
2
Experimental induction of premature movement of rat palatal shelves in vivo.大鼠腭板在体内过早移动的实验诱导
J Anat. 1979 Oct;129(Pt 3):597-601.
3
The influence of the epithelium on palate shelf reorientation.上皮组织对腭突重新定位的影响。
J Embryol Exp Morphol. 1985 Aug;88:265-79.
4
Cortisone-induced cleft palate in A/J mice: failure of palatal shelf contact.可的松诱导A/J小鼠腭裂:腭突接触失败
Teratology. 1981 Oct;24(2):149-62. doi: 10.1002/tera.1420240206.
5
Development of the secondary palate in the rat: a scanning electron microscopic study.大鼠继发腭的发育:一项扫描电子显微镜研究。
J Craniofac Genet Dev Biol. 1983;3(2):159-77.
6
Palatal shelf movement during palatogenesis: a fate map of the fetal mouse palate cultured in vitro.腭发育过程中的腭突运动:体外培养的胎鼠腭的命运图谱。
Anat Embryol (Berl). 2004 Apr;208(1):19-25. doi: 10.1007/s00429-004-0379-0. Epub 2004 Feb 21.
7
Cell distribution during mouse secondary palate closure. II. Mesenchymal cells.
J Embryol Exp Morphol. 1986 Jul;96:111-30.
8
A comparative study of craniofacial growth during secondary palate development in four strains of mice.四种品系小鼠继发腭发育过程中颅面生长的比较研究。
J Craniofac Genet Dev Biol. 1982;2(4):247-63.
9
Experimental induction of palate shelf elevation in glutamate decarboxylase 67-deficient mice with cleft palate due to vertically oriented palatal shelf.在因垂直取向的腭板而患有腭裂的谷氨酸脱羧酶67缺陷小鼠中实验性诱导腭板抬高。
Birth Defects Res A Clin Mol Teratol. 2007 Oct;79(10):688-95. doi: 10.1002/bdra.20400.
10
The effects of chlorcyclizine-induced alterations of glycosaminoglycans on mouse palatal shelf elevation in vivo and in vitro.氯环嗪诱导的糖胺聚糖改变对小鼠腭突在体内和体外抬高的影响。
J Embryol Exp Morphol. 1982 Jun;69:193-213.

引用本文的文献

1
Methods of Palate Culture in Later Palatogenesis: Elevation, Horizontal Outgrowth, and Fusion.腭部培养方法在腭发育后期:提升、水平生长和融合。
Methods Mol Biol. 2022;2403:63-80. doi: 10.1007/978-1-0716-1847-9_6.
2
Three-dimensional reconstruction of systematic histological sections: application to observations on palatal shelf elevation.系统性组织切片的三维重建:在腭突抬高观察中的应用
Int J Oral Sci. 2021 May 26;13(1):17. doi: 10.1038/s41368-021-00122-8.
3
Differences in Oral Structure and Tissue Interactions during Mouse vs. Human Palatogenesis: Implications for the Translation of Findings from Mice.
小鼠与人类腭发育过程中口腔结构和组织相互作用的差异:对小鼠研究结果转化的启示
Front Physiol. 2017 Mar 15;8:154. doi: 10.3389/fphys.2017.00154. eCollection 2017.
4
Mesenchymal Remodeling during Palatal Shelf Elevation Revealed by Extracellular Matrix and F-Actin Expression Patterns.通过细胞外基质和F-肌动蛋白表达模式揭示的腭突抬高过程中的间充质重塑
Front Physiol. 2016 Sep 7;7:392. doi: 10.3389/fphys.2016.00392. eCollection 2016.
5
Histomorphological study of palatal shelf elevation during murine secondary palate formation.腭突升高过程中鼠类次生腭形成的组织形态学研究。
Dev Dyn. 2011 Jul;240(7):1737-44. doi: 10.1002/dvdy.22670. Epub 2011 May 26.
6
Epithelial proliferation and development of rugae in relation to palatal shelf elevation in the mouse.小鼠腭皱襞上皮增殖与发育与腭突抬高的关系。
J Anat. 1984 Mar;138 ( Pt 2)(Pt 2):251-8.
7
Histochemical localization of glycosaminoglycans during morphogenesis of the secondary palate in mice.小鼠继发腭形态发生过程中糖胺聚糖的组织化学定位
Anat Embryol (Berl). 1985;173(1):137-42. doi: 10.1007/BF00707312.