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年龄依赖性增殖参与了小鼠小肠中 Cajal 间质细胞的出生后发育。

An age-dependent proliferation is involved in the postnatal development of interstitial cells of Cajal in the small intestine of mice.

作者信息

Mei Feng, Zhu Jiang, Guo Sheng, Zhou De-Shan, Han Juan, Yu Bin, Li Shi-Feng, Jiang Zhong-Yong, Xiong Cheng-Jie

机构信息

Department of Histology and Embryology, Third Military Medical University, 400038, Chongqing, China.

出版信息

Histochem Cell Biol. 2009 Jan;131(1):43-53. doi: 10.1007/s00418-008-0515-7. Epub 2008 Oct 3.

DOI:10.1007/s00418-008-0515-7
PMID:18836738
Abstract

This paper aimed at investigating the alterations in interstitial cells of Cajal (ICCs) in the murine small intestine from 0-day to 56-day post-partum (P0-P56) by immunohistochemistry. The Kit+ ICCs, which were situated around myenteric nerve plexus (ICC-MY) formed a loose cellular network at P0 which changed into an intact one before P32. The density of ICC-MY increased from P0 to P12, and then decreased until P32. In contrast, the estimated total amount increased more than 15-fold at P32 than that at P0. Some Kit+/BrdU+ cells were observed at 24 h after one BrdU injection to the different-aged mice, and the number decreased from P2 to P24 and vanished at P32. Actually a few Kit+/BrdU+ cells can be observed at 1 h after one BrdU injection at P10, and the amount doubled at 24 h along with paired Kit+/BrdU+ cells. A number of BrdU+ ICCs were also labeled with CD34, CD44 and insulin-like growth factor I receptor. About 65% ICCs were BrdU+ at P32 after daily BrdU injection from P0. Our results indicate that an age-dependent proliferation is involved in the postnatal development of ICC-MY which increase greatly in cell numbers and proliferative ICCs may originate from ICCs progenitor cells.

摘要

本文旨在通过免疫组织化学方法研究产后0天至56天(P0 - P56)小鼠小肠中Cajal间质细胞(ICC)的变化。位于肌间神经丛周围的Kit⁺ ICC(ICC - MY)在P0时形成松散的细胞网络,在P32之前转变为完整的网络。ICC - MY的密度从P0增加到P12,然后下降直至P32。相比之下,P32时估计的总量比P0时增加了15倍以上。在向不同年龄小鼠注射一次BrdU后24小时观察到一些Kit⁺/BrdU⁺细胞,其数量从P2减少到P24,并在P32时消失。实际上,在P10注射一次BrdU后1小时可观察到少数Kit⁺/BrdU⁺细胞,24小时时数量翻倍并伴有成对的Kit⁺/BrdU⁺细胞。许多BrdU⁺ ICC也被CD34、CD44和胰岛素样生长因子I受体标记。从P0开始每日注射BrdU后,P32时约65%的ICC为BrdU⁺。我们的结果表明,年龄依赖性增殖参与了ICC - MY的出生后发育,其细胞数量大幅增加,增殖性ICC可能起源于ICC祖细胞。

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本文引用的文献

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Progenitor cells of interstitial cells of Cajal: on the road to tissue repair.Cajal间质细胞的祖细胞:通往组织修复之路
Gastroenterology. 2008 Apr;134(4):1252-4. doi: 10.1053/j.gastro.2008.02.074.
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Progenitors of interstitial cells of cajal in the postnatal murine stomach.出生后小鼠胃中卡哈尔间质细胞的祖细胞。
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Kit signaling is essential for development and maintenance of interstitial cells of Cajal and electrical rhythmicity in the embryonic gastrointestinal tract.
起搏器网络中耦合强度和固有频率的空间噪声;根据弱耦合相位振荡器模型对肠道运动模式发展的影响。
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Walker 256 tumor-bearing rats demonstrate altered interstitial cells of Cajal. Effects on ICC in the Walker 256 tumor model.Walker 256荷瘤大鼠显示出 Cajal 间质细胞的改变。Walker 256肿瘤模型中对 Cajal 间质细胞的影响。
Neurogastroenterol Motil. 2016 Jan;28(1):101-15. doi: 10.1111/nmo.12702. Epub 2015 Nov 3.
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Interstitial cells: regulators of smooth muscle function.间质细胞:平滑肌功能的调节者。
Physiol Rev. 2014 Jul;94(3):859-907. doi: 10.1152/physrev.00037.2013.
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Developmental changes in postnatal murine intestinal interstitial cell of Cajal network structure and function.出生后小鼠肠道Cajal间质细胞网络结构和功能的发育变化
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Numerical metrics for automated quantification of interstitial cell of Cajal network structural properties.用于 Cajal 间质细胞网络结构特性自动量化的数值指标。
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