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小鼠Ror2受体酪氨酸激酶是心脏发育和肢体形成所必需的。

Mouse Ror2 receptor tyrosine kinase is required for the heart development and limb formation.

作者信息

Takeuchi S, Takeda K, Oishi I, Nomi M, Ikeya M, Itoh K, Tamura S, Ueda T, Hatta T, Otani H, Terashima T, Takada S, Yamamura H, Akira S, Minami Y

机构信息

Department of Biochemistry, Kobe University, School of Medicine, 7-5-1, Kusunoki-cho, Chuo-ku, Kobe 650-0017, Japan.

出版信息

Genes Cells. 2000 Jan;5(1):71-8. doi: 10.1046/j.1365-2443.2000.00300.x.

Abstract

BACKGROUND

A mouse receptor tyrosine kinase (RTK), mRor2, which belongs to the Ror-family of RTKs consisting of at least two structurally related members, is primarily expressed in the heart and nervous system during mouse development. To elucidate the function of mRor2, we generated mice with a mutated mRor2 locus.

RESULTS

Mice with a homozygous mutation in mRor2 died just after birth, exhibiting dwarfism, severe cyanosis, and short limbs and tails. Whole-mount in situ hybridization analysis showed that mRor2 was expressed in the branchial arches, heart and limb/tailbuds, in addition to the developing nervous system. The mutants had cardiac septal defects, mainly a ventricular septal defect. In addition, an examination of the skeletal systems revealed that the mutants had shorter limbs, vertebrae and facial structure, with a particular defect in their distal portions, and that almost no calcification was observed in their distal limbs. Histological examination showed abnormalities in the chondrocytes.

CONCLUSIONS

Our findings suggest that mRor2 plays essential roles in the development of the heart and in limb/tail formation, in particular cardiac septal formation and ossification of distal portions of limbs and tails.

摘要

背景

小鼠受体酪氨酸激酶(RTK)mRor2属于RTK的Ror家族,该家族至少由两个结构相关的成员组成,在小鼠发育过程中主要表达于心脏和神经系统。为了阐明mRor2的功能,我们构建了mRor2基因座发生突变的小鼠。

结果

mRor2纯合突变的小鼠出生后不久即死亡,表现出侏儒症、严重发绀以及四肢和尾巴短小。整体原位杂交分析表明,除了发育中的神经系统外,mRor2在鳃弓、心脏以及肢体/尾芽中也有表达。突变体存在心脏间隔缺损,主要是室间隔缺损。此外,对骨骼系统的检查发现,突变体的四肢、椎骨和面部结构较短,其远端部分存在特定缺陷,并且在其远端肢体中几乎未观察到钙化。组织学检查显示软骨细胞存在异常。

结论

我们的研究结果表明,mRor2在心脏发育以及肢体/尾巴形成中发挥重要作用,特别是在心脏间隔形成以及肢体和尾巴远端部分的骨化过程中。

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