音猬因子与胰岛素增强子结合蛋白在小鼠胚胎呼吸系统的早期表达

蔡玉瑾 李慧超 张宏权 景雅 杨艳萍 崔慧林

解剖学报 ›› 2016, Vol. 47 ›› Issue (5) : 678-682.

PDF(646 KB)
欢迎访问《解剖学报》官方网站!今天是 English
PDF(646 KB)
解剖学报 ›› 2016, Vol. 47 ›› Issue (5) : 678-682. DOI: 10.16098/j.issn.0529-1356.2016.05.018
组织学胚胎学发育生物学

音猬因子与胰岛素增强子结合蛋白在小鼠胚胎呼吸系统的早期表达

  • 蔡玉瑾1 李慧超2 张宏权3 景雅1* 杨艳萍1 崔慧林1
作者信息 +

Expression of sonic hedgehog and islet-1 in morphogenesis of respiratory system in mouse embryo

  • CAI Yu-jin1 LI Hui-chao2 ZHANG Hong-quan3 JING Ya 1* YANG Yan-ping1 CUI Hui-lin1
Author information +
文章历史 +

摘要

目的 探讨音猬因子信号通路成员与胰岛素增强子结合蛋白在呼吸系统的早期表达与其发育的联系。方法 胚龄9.0~13d小鼠胚胎呼吸系统各年龄段不小于3个,连续石蜡切片,用抗音猬因子(Shh)、抗patched1(Ptcl)、抗smoothened(Smo)、抗胰岛素增强子结合蛋白(ISL1)和抗α-平滑肌肌动蛋白(α-SMA)抗体进行免疫组织化学染色。结果 胚龄10d,Shh表达在前肠内胚层腹侧壁。胚龄11~12d,Ptc1表达在气管、支气管和肺内分支上皮。胚龄13d,Ptc1只表达在肺内分支上皮。胚龄9d,ISL1表达在前肠内胚层腹侧壁。胚龄10~12d,ISL1表达在前肠(气管)腹侧壁和支气管侧壁上皮及邻近的间充质内。胚龄13d,ISL1表达减弱,始终未见在肺内有阳性表达。胎龄12~13d,与气管后壁、支气管内侧壁上皮Ptc1表达减弱处相邻的间充质出现α-SMA阳性平滑肌细胞,其与对侧间充质ISL1阳性细胞的分布呈背-腹侧或内-外侧模式。气管腹侧及肺芽外侧间充质中可见ISL1与Smo共表达细胞。 结论 ISL1在气管及肺芽的发育中可能与Shh信号系统协同发挥作用。

Abstract

Objective To explore the relationship of the early morphogenesis of respiratory system with the expression of islet-1(ISL1) and sonic hedgehog(Shh)-patched 1(Ptc1)-smoothened(Smo) pathway.Methods Serial sections of three mouse embryos each day from embryonic day(ED) 9.0 to ED 13 were stained immunohistochemically with antibodies against Shh, Ptcl, Smo, ISL1 and α-smooth muscle actin (α-SMA).Results At ED10, Shh was detected in the endodermal epithelium ventral to the foregut. From ED11 to ED12, Ptc1 was present in epithelial cells of both the trachea, bronchies and branching of lung buds. At ED13, Ptc1 expression was restricted to epithelial cells of airway in lung. At ED9, ISL1 staining of epithelial cells was observed in endoderm ventral to the foregut. From ED11 to ED12, ISL1 staining was observed in epithelial and mesenchyme cells surrounding ventral to the trachea and lateral to the bronchies, where colocalization of ISL1 with Smo was detected. At ED13, ISL1 staining was reduced, while little present in the distal airway of the developing lung. From ED12 to ED13, α-SMA positive smooth muscle cells were detected in mesenchyme adjacent closely to the dorsal wall of trachea and between bronchies where Ptc1 staining was negative in the epithelial. The distribution pattern of ISL1 positive cells and α-SMA positive cells in mesenchyme around trachea and bronchies was in dorsal-ventral or inner-lateral direction.Conclusion ISL1 may play an important role in normal morphogenesis of the trachea and lung buds in coordination with members of Shh-Ptc1-Smo pathway.

关键词

音猬因子 / 胰岛素增强子结合蛋白 / 呼吸系统 / 胚胎 / 免疫组织化学 / 小鼠

Key words

Sonic hedgehog / Islet-1 Respiratory system| Embryo| Immunohistochemistry| Mouse

引用本文

导出引用
蔡玉瑾 李慧超 张宏权 景雅 杨艳萍 崔慧林. 音猬因子与胰岛素增强子结合蛋白在小鼠胚胎呼吸系统的早期表达[J]. 解剖学报. 2016, 47(5): 678-682 https://doi.org/10.16098/j.issn.0529-1356.2016.05.018
CAI Yu-jin LI Hui-chao ZHANG Hong-quan JING Ya YANG Yan-ping CUI Hui-lin. Expression of sonic hedgehog and islet-1 in morphogenesis of respiratory system in mouse embryo[J]. Acta Anatomica Sinica. 2016, 47(5): 678-682 https://doi.org/10.16098/j.issn.0529-1356.2016.05.018

参考文献

[1]Litingtung Y, Lei L, Westphal H, et al. Sonic hedgehog is essential to foregut development[J]. Nat Genet, 1998,20(1):58-61.
[2]Cardoso WV, Lü J. Regulation of early lung morphogenesis: questions, facts and controversies[J]. Development, 2006,133(9):1611-1624.
[3]Jacobs IJ, Ku WY, Que J. Genetic and cellular mechanisms regulating anterior foregut and esophageal development[J]. Dev Biol, 2012, 369(1):54-64.
[4]Warburton D, Bellusci S, De Langhe S, et al. Molecular mechanisms of early lung specification and branching morphogenesis[J]. Pediatr Res, 2005, 57(5 Pt 2):26R-37R.
[5]Urase K, Mukasa T, Igarashi H, et al. Spatial expression of Sonic hedgehog in the lung epithelium during branching morphogenesis[J]. Biochem Biophys Res Commun, 1996, 225(1):161-166.
[6]Cai CL, Liang X, Shi Y, et al. Isl1 identifies a cardiac progenitor population that proliferates prior to differentiation and contributes a majority of cells to the heart[J]. Dev Cell, 2003, 5(6):877-889.
[7]Mendelson CR. Role of transcription factors in fetal lung development and surfactant protein gene expression[J]. Annu Rev Physiol, 2000, 62:875-915.
[8]Liang S, Li HC, Wang YX, et al. Pulmonary endoderm, second heart field and the morphogenesis of distal outflow tract in mouse embryonic heart[J]. Dev Growth Differ, 2014, 56(4):276-292.
[9]Li HCh, Jing Y, Shi L, et al. Association of morphogenesis of pulmonary endoderm with development of prepharyngeal mesenchyme and outflow tract septation in mouse embryos[J]. Acta Anatomica Sinica, 2013, 44 (6): 804-811. (in Chinese)
李慧超, 景雅, 师亮, 等. 小鼠胚胎呼吸内胚层形态发生与咽前间充质发育及流出道分隔的关系[J]. 解剖学报, 2013, 44(6):804-811.
[10]Cai YJ, Jing Y, Qiao AX, et al.Coupling of heart outflow tract morphogenesis with development of pulmonary endoderm in mouse embryo[J]. Acta Anatomica Sinica, 2012, 43(6):802-806.(in Chinese)
蔡玉瑾, 景雅, 乔爱秀, 等. 小鼠胚胎心流出道的形态发生与呼吸内胚层发育耦联[J]. 解剖学报, 2012,43(06):802-806.
[11]Miller LA, Wert SE, Clark JC, et al. Role of Sonic hedgehog in patterning of tracheal-bronchial cartilage and the peripheral lung[J]. Dev Dyn, 2004, 231(1):57-71.
[12]Incardona JP, Gruenberg J, Roelink H. Sonic hedgehog induces the segregation of patched and smoothened in endosomes[J]. Curr Biol, 2002, 12(12):983-995.
[13]Ahlgren U, Pfaff  SL, Jessell TM, et al. Independent requirement for ISL1 in formation of pancreatic mesenchyme and islet cells[J]. Nature, 1997, 385(6613):257-260.
[14]Lin L, Bu L, Cai CL, et al. Isl1 is upstream of sonic hedgehog in a pathway required for cardiac morphogenesis[J]. Dev Biol, 2006, 295(2):756-763.
[15]Zou L, Guo JS, Dai X, et al. Effect of sonic hedgehog on the proliferation and differentitation of neural stem cells[J]. Acta Anatomica Sinica, 2009, 40(2):211-214. (in Chinese)
邹琳, 郭家松, 戴翔, 等. 音猬因子对神经干细胞增殖与分化的影响[J]. 解剖学报, 2009,40(2):211-214.
[16]Hogan BL, Yingling JM. Epithelial/mesenchymal interactions and branching morphogenesis of the lung[J]. Curr Opin Genet Dev, 1998, 8(4):481-486.
[17]Park J, Zhang JJ, Moro A, et al. Regulation of Sox9 by Sonic Hedgehog (Shh) is essential for patterning and formation of tracheal cartilage[J]. Dev Dyn, 2010, 239(2):514-526.
[18]Tollet J, Everett AW, Sparrow MP. Spatial and temporal distribution of nerves, ganglia, and smooth muscle during the early pseudoglandular stage of fetal mouse lung development[J]. Dev Dyn, 2001, 221(1):48-60.
[19]Gopalakrishnan S, Comai G, Sambasivan R, et al. A Cranial Mesoderm Origin for Esophagus Striated Muscles[J]. Dev Cell, 2015, 34(6):694-704.
[20]Badri KR, Zhou Y, Schuger L. Embryological origin of airway smooth muscle[J]. Proc Am Thorac Soc, 2008, 5(1):4-10.
[21]Li Y, Zhang H, Choi SC, et al. Sonic hedgehog signaling regulates Gli3 processing, mesenchymal proliferation, and differentiation during mouse lung organogenesis[J]. Dev Biol, 2004, 270(1):214-231.
[22]Morrisey EE, Hogan BL. Preparing for the first breath: genetic and cellular mechanisms in lung development[J]. Dev Cell, 2010, 18(1):8-23.
[23]Peng T, Tian Y, Boogerd CJ, et al. Coordination of heart and lung co-development by a multipotent cardiopulmonary progenitor[J]. Nature, 2013, 500(7464):589-592.
[24]Perl AK, Wert SE, Nagy A, et al. Early restriction of peripheral and proximal cell lineages during formation of the lung[J]. Proc Natl Acad Sci USA, 2002, 99(16):10482-10487.

基金

人胚胎第二生心区和心脏流出道的发育;小鼠胚胎心背侧间充质突与心房发育;山西省优势学科资助项目;山西医科大学博士启动基金


PDF(646 KB)

Accesses

Citation

Detail

段落导航
相关文章

/