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血浆外泌体 miRNA-26b-3p 来源于特发性身材矮小,通过 AKAP2/ERK1/2 轴损害纵向骨生长。

Plasma exosome miRNA-26b-3p derived from idiopathic short stature impairs longitudinal bone growth via the AKAP2/ERK1/2 axis.

机构信息

Department of Pediatrics, The Second Affiliated Hospital of Nanchang University, Nanchang City, Jiangxi Province, China.

Department of Orthopedics, The Second Affiliated Hospital of Nanchang University, Nanchang City, 330006, Jiangxi Province, China.

出版信息

J Nanobiotechnology. 2023 Mar 16;21(1):94. doi: 10.1186/s12951-023-01849-8.

Abstract

BACKGROUND

Currently, the etiology of idiopathic short stature (ISS) is still unclear. The poor understanding of the molecular mechanisms of ISS has largely restricted this strategy towards safe and effective clinical therapies.

METHODS

The plasma exosomes of ISS children were co-cultured with normal human chondrocytes. The differential expression of exosome miRNA between ISS and normal children was identified via high-throughput microRNA sequencing and bioinformatics analysis. Immunohistochemistry, In situ hybridization, RT-qPCR, western blotting, luciferase expression, and gene overexpression and knockdown were performed to reveal the key signaling pathways that exosome miRNA of aberrant expression in ISS children impairs longitudinal bone growth.

RESULTS

Chondrocytes proliferation and endochondral ossification were suppressed after coculture of ISS plasma exosomes with human normal chondrocytes. High-throughput microRNA sequencing and RT-qPCR confirmed that plasma exosome miR-26b-3p was upregulated in ISS children. Meanwhile, exosome miRNA-26b-3p showed a high specificity and sensitivity in discriminating ISS from normal children. The rescue experiment showed that downregulation of miR-26b-3p obviously improved the repression of chondrocyte proliferation and endochondral ossification caused by ISS exosomes. Subsequently, miR-26b-3p overexpression inhibited chondrocyte proliferation and endochondral ossification once again. In situ hybridization confirmed the colocalization of miR-26b-3p with AKAP2 in chondrocytes. In vitro and in vivo assay revealed exosome miRNA-26b-3p impairs longitudinal bone growth via the AKAP2 /ERK1/2 axis.

CONCLUSIONS

This study is the first to confirm that miR-26b-3p overexpression in ISS plasma exosomes leads to disorders in proliferation and endochondral ossification of growth plate cartilage via inhibition of AKAP2/ERK1/2 axis, thereby inducing ISS. This study provides a new research direction for the etiology and pathology of ISS and a new idea for the biological treatment of ISS.

摘要

背景

目前,特发性身材矮小(ISS)的病因仍不清楚。对 ISS 分子机制的认识不足,在很大程度上限制了这一策略向安全有效的临床治疗的发展。

方法

将 ISS 儿童的血浆外泌体与正常人软骨细胞共培养。通过高通量 microRNA 测序和生物信息学分析鉴定 ISS 儿童与正常儿童外泌体 miRNA 的差异表达。采用免疫组化、原位杂交、RT-qPCR、Western blot、荧光素酶表达、基因过表达和敲低等方法,揭示了 ISS 儿童异常表达的外泌体 miRNA 损害纵向骨生长的关键信号通路。

结果

ISS 儿童血浆外泌体与人正常软骨细胞共培养后,软骨细胞增殖和软骨内骨化受到抑制。高通量 microRNA 测序和 RT-qPCR 证实,ISS 儿童血浆外泌体 miR-26b-3p 上调。同时,外泌体 miRNA-26b-3p 在区分 ISS 和正常儿童方面具有较高的特异性和敏感性。挽救实验表明,下调 miR-26b-3p 可明显改善 ISS 外泌体对软骨细胞增殖和软骨内骨化的抑制作用。随后,miR-26b-3p 的过表达再次抑制软骨细胞的增殖和软骨内骨化。原位杂交证实 miR-26b-3p 与软骨细胞中的 AKAP2 共定位。体外和体内实验表明,外泌体 miRNA-26b-3p 通过 AKAP2/ERK1/2 轴损害纵向骨生长。

结论

本研究首次证实,ISS 儿童血浆外泌体中 miR-26b-3p 的过表达通过抑制 AKAP2/ERK1/2 轴导致生长板软骨增殖和软骨内骨化紊乱,从而诱导 ISS。本研究为 ISS 的病因和发病机制提供了新的研究方向,为 ISS 的生物学治疗提供了新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62c2/10022307/b8b651270808/12951_2023_1849_Fig1_HTML.jpg

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