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Foxn1基因缺陷(裸)小鼠皮肤中基因表达的幼态延续现象——再生性皮肤伤口愈合的一种预测

Neotenic phenomenon in gene expression in the skin of Foxn1- deficient (nude) mice - a projection for regenerative skin wound healing.

作者信息

Kur-Piotrowska Anna, Kopcewicz Marta, Kozak Leslie P, Sachadyn Pawel, Grabowska Anna, Gawronska-Kozak Barbara

机构信息

Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, ul. Tuwima 10, 10-748, Olsztyn, Poland.

Department of Molecular Biotechnology and Microbiology, Gdansk University of Technology, ul. G. Narutowicza 11/12, 80-233, Gdansk, Poland.

出版信息

BMC Genomics. 2017 Jan 9;18(1):56. doi: 10.1186/s12864-016-3401-z.

Abstract

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.

摘要

背景

胚胎发育至16天的小鼠胎儿以及裸鼠(Foxn1基因缺陷型)是能够实现再生性(无瘢痕)皮肤愈合的动物实例。转录因子Foxn1在小鼠胎儿表皮中的表达始于胚胎第16.5天,这与皮肤伤口愈合从无瘢痕到形成瘢痕的转变点相吻合。在本研究中,我们检验了以下假设:皮肤中Foxn1的表达是建立成年皮肤表型的必要条件,并且裸鼠中Foxn1的失活使皮肤处于类似于幼态持续现象的未成熟阶段。

结果

通过RNA测序对成年C57BL/6J(B6)小鼠、胚胎发育第14天(E14)和第18天(E18)的小鼠胎儿以及B6.Cg-Foxn1nu(裸)小鼠的未受伤皮肤进行基因表达谱分析,并通过qRT-PCR、蛋白质免疫印迹和免疫组织化学进行验证。差异调节基因表明,裸鼠与E14(再生性愈合模型)更为相似,而B6小鼠与E18(修复性愈合模型)更为相似。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相关,而下调的基因与分化相关。E14和裸鼠表现出角蛋白(Krt23、-73、-82、-16、-17)、内披蛋白(Ivl)和丝聚合蛋白(Flg2)基因的显著上调。在胚胎发育过程中已知可指定细胞命运并促进胚胎干细胞分化的与Hox基因相关的转录因子在裸鼠和E14中均下调。在裸鼠皮肤中富集但未在E14胎儿中共享的基因中,有Wnt家族和基质金属蛋白酶(Mmps)家族的成员,而Bmp和Notch相关基因下调。

结论

总之,Foxn1似乎是发育程序和皮肤成熟的关键控制元件。裸鼠可被视为哺乳动物中的幼态持续模型。裸鼠和E14小鼠皮肤中基因表达谱的相似性是Foxn1缺陷的直接或间接后果。Foxn1似乎调节细胞增殖与分化之间的平衡,其失活创造了一个促进再生的环境。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c425/5223329/c9584597f59c/12864_2016_3401_Fig1_HTML.jpg

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