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蝾螈晶状体再生的可塑性与基因表达中与年龄相关的变化有关。

Plasticity for axolotl lens regeneration is associated with age-related changes in gene expression.

作者信息

Sousounis Konstantinos, Athippozhy Antony T, Voss S Randal, Tsonis Panagiotis A

机构信息

Department of Biology and Center for Tissue Regeneration and Engineering University of Dayton Dayton OH USA.

Department of Biology and Spinal Cord and Brain Injury Research Center University of Kentucky Lexington KY 40503 USA.

出版信息

Regeneration (Oxf). 2014 Oct 12;1(3):47-57. doi: 10.1002/reg2.25. eCollection 2014 Jun.

Abstract

Mexican axolotls lose potential for lens regeneration 2 weeks after hatching. We used microarrays to identify differently expressed genes before and after this critical time, using RNA isolated from iris. Over 3700 genes were identified as differentially expressed in response to lentectomy between young (7 days post-hatching) and old (3 months post-hatching) axolotl larvae. Strikingly, many of the genes were only expressed in the early or late iris. Genes that were highly expressed in young iris significantly enriched electron transport chain, transcription, metabolism, and cell cycle gene ontologies, all of which are associated with lens regeneration. In contrast, genes associated with cellular differentiation and tissue maturation were uniquely expressed in old iris. Many of these expression differences strongly suggest that young and old iris samples were collected before and after the spleen became developmentally competent to produce and secrete cells with humoral and innate immunity functions. Our study establishes the axolotl as a powerful model to investigate age-related cellular differentiation and immune system ontogeny within the context of tissue regeneration.

摘要

墨西哥钝口螈在孵化后2周失去晶状体再生能力。我们使用微阵列,通过从虹膜中分离的RNA,来鉴定这一关键时间前后差异表达的基因。超过3700个基因被鉴定为在幼体(孵化后7天)和老体(孵化后3个月)墨西哥钝口螈幼体中因晶状体切除而差异表达。令人惊讶的是,许多基因仅在虹膜早期或晚期表达。在幼体虹膜中高表达的基因显著富集了电子传递链、转录、代谢和细胞周期基因本体,所有这些都与晶状体再生相关。相比之下,与细胞分化和组织成熟相关的基因在老体虹膜中独特表达。这些表达差异中的许多强烈表明,幼体和老体虹膜样本分别是在脾脏发育成熟以产生和分泌具有体液免疫和先天免疫功能的细胞之前和之后收集的。我们的研究将墨西哥钝口螈确立为一个强大的模型,用于在组织再生的背景下研究与年龄相关的细胞分化和免疫系统个体发育。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29fe/4895297/bc291d26712f/REG2-1-47-g001.jpg

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