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首页> 外文期刊>BMC Genomics >Neotenic phenomenon in gene expression in the skin of Foxn1- deficient (nude) mice - a projection for regenerative skin wound healing
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Neotenic phenomenon in gene expression in the skin of Foxn1- deficient (nude) mice - a projection for regenerative skin wound healing

机译:Foxn1缺陷(裸)小鼠皮肤中基因表达的新生物现象-再生皮肤伤口愈合的预测

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Background Mouse fetuses up to 16?day of embryonic development and nude (Foxn1- deficient) mice are examples of animals that undergo regenerative (scar-free) skin healing. The expression of transcription factor Foxn1 in the epidermis of mouse fetuses begins at embryonic day 16.5 which coincides with the transition point from scar-free to scar-forming skin wound healing. In the present study, we tested the hypothesis that Foxn1 expression in the skin is an essential condition to establish the adult skin phenotype and that Foxn1 inactivity in nude mice keeps skin in the immature stage resembling the phenomena of neoteny. Results Uninjured skin of adult C57BL/6J (B6) mice, mouse fetuses at days 14 (E14) and 18 (E18) of embryonic development and B6.Cg-Foxn1 nu (nude) mice were characterized for their gene expression profiles by RNA sequencing that was validated through qRT-PCR, Western Blot and immunohistochemistry. Differentially regulated genes indicated that nude mice were more similar to E14 (model of regenerative healing) and B6 were more similar to E18 (model of reparative healing). The up-regulated genes in nude and E14 mice were associated with tissue remodeling, cytoskeletal rearrangement, wound healing and immune response, whereas the down-regulated genes were associated with differentiation. E14 and nude mice exhibit prominent up-regulation of keratin (Krt23, -73, -82, -16, -17), involucrin (Ivl) and filaggrin (Flg2) genes. The transcription factors associated with the Hox genes known to specify cell fate during embryonic development and promote embryonic stem cells differentiation were down-regulated in both nude and E14. Among the genes enriched in the nude skin but not shared with E14 fetuses were members of the Wnt and matrix metalloproteinases (Mmps) families whereas Bmp and Notch related genes were down-regulated. Conclusions In summary, Foxn1 appears to be a pivotal control element of the developmental program and skin maturation. Nude mice may be considered as a model of neoteny among mammals. The resemblance of gene expression profiles in the skin of both nude and E14 mice are direct or indirect consequences of the Foxn1 deficiency. Foxn1 appears to regulate the balance between cell proliferation and differentiation and its inactivity creates a pro-regenerative environment.
机译:背景技术胚胎发育长达16天的小鼠胎儿和裸(Foxn1缺陷型)小鼠是经历再生(无疤痕)皮肤愈合的动物的例子。小鼠胎儿表皮中转录因子Foxn1的表达始于胚胎第16.5天,这与从无疤痕到形成疤痕的皮肤伤口愈合的转变点相吻合。在本研究中,我们测试了以下假设:皮肤中Foxn1的表达是建立成年皮肤表型的必要条件,而在裸鼠中Foxn1的失活使皮肤处于未成熟阶段,类似于新生现象。结果成年C57BL / 6J(B6)小鼠,胚胎发育第14天(E14)和第18天(E18)的小鼠胎儿和B6的未损伤皮肤.Cg-Foxn1 nu(nude)小鼠通过RNA测序表征其基因表达谱通过qRT-PCR,Western Blot和免疫组织化学验证。差异调节基因表明,裸鼠与E14(再生愈合模型)更相似,而B6与E18(再生愈合模型)更相似。裸鼠和E14小鼠中上调的基因与组织重塑,细胞骨架重排,伤口愈合和免疫反应有关,而下调的基因与分化有关。 E14和裸鼠表现出明显的上调角蛋白(Krt23,-73,-82,-16,-17),整合素(Ivl)和丝聚蛋白(Flg2)基因。与Hox基因相关的转录因子在裸子和E14中均被下调,而Hox基因已知可在胚胎发育过程中确定细胞命运并促进胚胎干细胞分化。在Wnt和基质金属蛋白酶(Mmps)家族中,富集于裸皮但不与E14胎儿共享的基因中,而Bmp和Notch相关基因则被下调。结论总之,Foxn1似乎是发育程序和皮肤成熟的关键控制因素。裸鼠可被认为是哺乳动物间新足动物的模型。裸鼠和E14小鼠皮肤中基因表达谱的相似性是Foxn1缺乏症的直接或间接后果。 Foxn1似乎调节细胞增殖与分化之间的平衡,并且其无活性创造了一种促进再生的环境。

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