耳廓的生长和分化在小鼠中是保守的,并且需要BMP信号来促进软骨细胞增殖。

IF 3.6 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY Development Pub Date : 2025-02-01 Epub Date: 2025-02-13 DOI:10.1242/dev.204560
Robyn S Allen, Shishir K Biswas, Ashley W Seifert
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引用次数: 0

摘要

尽管耳廓的发育是重建手术的主要目标,但对耳廓发育的研究仍然很少。在这里,我们提供了两种啮齿动物妊娠晚期和出生后耳廓发育的细胞特征,并研究了BMP5在耳廓弹性软骨扩张和分化中的作用。我们发现,在小家鼠和高度再生的小家鼠之间,耳廓发育在很大程度上是保守的。软骨前细胞的模式是在发育早期建立的。这些细胞在耳朵展开之前被指定为成软骨细胞,然后在成熟之前经历广泛的增殖。成人耳廓的弹性软骨、结缔组织成纤维细胞、真皮乳头和鞘细胞、脂肪细胞来源于颅神经嵴。使用自然发生的短耳小鼠突变体的细胞分析表明,BMP5的缺失不会阻止成软骨细胞的特异性,但会损害它们的增殖。最后,这些突变体的成年中远端耳廓的成软骨细胞增殖仍然受损。这些数据共同建立了耳廓组织分化的发育基础。
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Ear pinna growth and differentiation is conserved in murids and requires BMP signaling for chondrocyte proliferation.

Despite being a major target of reconstructive surgery, development of the ear pinna remains poorly studied. Here, we provide a cellular characterization of late gestational and postnatal ear pinna development in two rodents and investigate the role of BMP5 in expansion and differentiation of auricular elastic cartilage. We find that ear pinna development is largely conserved between Mus musculus and the highly regenerative Acomys dimidiatus. The pattern of pre-cartilaginous cells is established early in development. These cells are specified into chondroblasts before ear unfolding and then undergo extensive proliferation before maturation. The elastic cartilage, connective tissue fibroblasts, dermal papilla and sheath cells, and adipocytes in the adult pinna are derived from cranial neural crest. Cellular analysis using the naturally occurring short ear mouse mutant shows that loss of BMP5 does not prevent specification of chondroblasts, but does impair chondroblast proliferation. Finally, chondroblast proliferation remains impaired in the adult mid-distal ear pinna of these mutants. Together, these data establish the developmental basis for differentiation of ear pinna tissues.

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来源期刊
Development
Development 生物-发育生物学
CiteScore
6.70
自引率
4.30%
发文量
433
审稿时长
3 months
期刊介绍: Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community. Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication. To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.
期刊最新文献
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