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6-氨基烟酰胺诱导及遗传性唇裂小鼠胚胎的有丝分裂指数

Mitotic index in mouse embryos with 6-aminonicotinamide-induced and inherited cleft lip.

作者信息

Trasler D G, Leong S

出版信息

Teratology. 1982 Apr;25(2):259-65. doi: 10.1002/tera.1420250215.

DOI:10.1002/tera.1420250215
PMID:7101202
Abstract

Three types of cleft lip were studied histologically before and during lip formation in mouse embryos. C57BL/6 embryos observed near term following treatment with 6-aminonicotinamide (6AN) at gestation D9/12 (vp day = day 0) had 18% median cleft lip. Treated embryos observed at D10 and D11 showed retarded somite and nasal placode development. Sections at lip closure time showed marked reduction of medial and some reduction of lateral nasal processes, and the mitotic index was significantly reduced in the nasal area on D10 and D11 but less consistently in the neural area. 6AN-treatment on D10/8, caused 22% lateral cleft lip. Treated embryos showed initial retardation of somite and nasal placode development that became normal by D11/14. Sections showed reduction of the medial and lateral nasal processes, and less organized denser nasal ectoderm. The mitotic index was significantly reduced in the nasal and neural areas on D10 and D11. In crosses having the major gene mutation dancer (Dc) 20% of embryos had lateral cleft lip and potential cleft lip mutant embryos showed reduced lateral and medial nasal processes. Mitotic index was not reduced in the nasal area but it was in the neural area. The CL/Fr strain, with a predisposing face shape in which 26% of the embryos have cleft lip of multifactorial origin, had a mitotic index similar to that of C57BL/6 (0% cleft lip) at lip closure time, D11/14, and prominent medial nasal processes. It is postulated that 6AN-induced median cleft lip is due to reduced cell proliferation in and size of the medial nasal processes; 6AN-induced lateral cleft lip to reduced cell proliferation and reduced medial and lateral nasal processes and dancer lateral cleft lip to reduction of the medial nasals.

摘要

在小鼠胚胎唇形成之前及期间,对三种类型的唇裂进行了组织学研究。在妊娠第9/12天(阴道栓日 = 第0天)用6 - 氨基烟酰胺(6AN)处理后接近足月时观察到的C57BL/6胚胎,有18%出现正中唇裂。在第10天和第11天观察到的经处理胚胎显示体节和鼻基板发育迟缓。唇闭合时的切片显示内侧鼻突明显减少,外侧鼻突有所减少,并且在第10天和第11天鼻区的有丝分裂指数显著降低,但在神经区不太一致。在第10/8天用6AN处理导致22%出现外侧唇裂。经处理的胚胎显示体节和鼻基板发育最初迟缓,到第11/14天恢复正常。切片显示内侧和外侧鼻突减少,鼻外胚层组织较疏松且密度更高。在第10天和第11天,鼻区和神经区的有丝分裂指数显著降低。在具有主要基因突变“舞者”(Dc)的杂交后代中,20%的胚胎有外侧唇裂,潜在的唇裂突变胚胎显示外侧和内侧鼻突减少。鼻区的有丝分裂指数未降低,但神经区降低。CL/Fr品系具有易患唇裂的面部形状,其中26%的胚胎有多因素起源的唇裂,在唇闭合时(第11/14天)有丝分裂指数与C57BL/6(0%唇裂)相似,且内侧鼻突突出。据推测,6AN诱导的正中唇裂是由于内侧鼻突中细胞增殖减少和大小减小;6AN诱导的外侧唇裂是由于细胞增殖减少以及内侧和外侧鼻突减少,而“舞者”外侧唇裂是由于内侧鼻突减少。

相似文献

1
Mitotic index in mouse embryos with 6-aminonicotinamide-induced and inherited cleft lip.6-氨基烟酰胺诱导及遗传性唇裂小鼠胚胎的有丝分裂指数
Teratology. 1982 Apr;25(2):259-65. doi: 10.1002/tera.1420250215.
2
Ultrastructure of initial nasal process cell fusion in spontaneous and 6-aminonicotinamide-induced mouse embryo cleft lip.自发及6-氨基烟酰胺诱导的小鼠胚胎唇裂中原始鼻突细胞融合的超微结构
Teratology. 1983 Aug;28(1):91-101. doi: 10.1002/tera.1420280112.
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Morphometric analysis of heterozygote dancer mice predisposed to 6-aminonicotinamide-induced cleft lip.对易患6-氨基烟酰胺诱导性唇裂的杂合子舞者小鼠进行形态计量分析。
Teratology. 1992 Apr;45(4):393-400. doi: 10.1002/tera.1420450410.
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Increased susceptibility to 6-aminonicotinamide-induced cleft lip of heterozygote Dancer mice.杂合子舞者小鼠对6-氨基烟酰胺诱导的唇裂易感性增加。
Teratology. 1984 Feb;29(1):101-4. doi: 10.1002/tera.1420290112.
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Comparative morphometrics of embryonic facial morphogenesis: implications for cleft-lip etiology.胚胎面部形态发生的比较形态计量学:对唇裂病因学的启示
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Test of the hypothesis that embryonic face shape is a causal factor in genetic predisposition to cleft lip in mice.关于胚胎面部形状是小鼠唇裂遗传易感性的一个因果因素这一假设的检验。
Teratology. 1976 Aug;14(1):35-41. doi: 10.1002/tera.1420140106.

引用本文的文献

1
Gene datasets associated with mouse cleft palate.与小鼠腭裂相关的基因数据集。
Data Brief. 2018 Mar 14;18:655-673. doi: 10.1016/j.dib.2018.03.010. eCollection 2018 Jun.
2
The cleft lip and palate defects in Dancer mutant mice result from gain of function of the Tbx10 gene.舞者突变小鼠的唇腭裂缺陷是由Tbx10基因的功能获得所致。
Proc Natl Acad Sci U S A. 2004 May 4;101(18):7022-7. doi: 10.1073/pnas.0401025101. Epub 2004 Apr 26.