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神经介素B通过钙调神经磷酸酶和钙信号传导促进间充质基质细胞的软骨细胞分化。

Neuromedin B promotes chondrocyte differentiation of mesenchymal stromal cells via calcineurin and calcium signaling.

作者信息

Maumus Marie, Fonteneau Guillaume, Ruiz Maxime, Assou Said, Boukhaddaoui Hassan, Pastoureau Philippe, De Ceuninck Frédéric, Jorgensen Christian, Noel Danièle

机构信息

IRMB, Univ Montpellier, INSERM, Montpellier, France.

INM, University of Montpellier, INSERM, CHU Montpellier, Montpellier, France.

出版信息

Cell Biosci. 2021 Oct 18;11(1):183. doi: 10.1186/s13578-021-00695-1.

Abstract

BACKGROUND

Articular cartilage is a complex tissue with poor healing capacities. Current approaches for cartilage repair based on mesenchymal stromal cells (MSCs) are often disappointing because of the lack of relevant differentiation factors that could drive MSC differentiation towards a stable mature chondrocyte phenotype.

RESULTS

We used a large-scale transcriptomic approach to identify genes that are modulated at early stages of chondrogenic differentiation using the reference cartilage micropellet model. We identified several modulated genes and selected neuromedin B (NMB) as one of the early and transiently modulated genes. We found that the timely regulated increase of NMB was specific for chondrogenesis and not observed during osteogenesis or adipogenesis. Furthermore, NMB expression levels correlated with the differentiation capacity of MSCs and its inhibition resulted in impaired chondrogenic differentiation indicating that NMB is required for chondrogenesis. We further showed that NMB activated the calcineurin activity through a Ca-dependent signaling pathway.

CONCLUSION

NMB is a newly described chondroinductive bioactive factor that upregulates the key chondrogenic transcription factor Sox9 through the modulation of Ca signaling pathway and calcineurin activity.

摘要

背景

关节软骨是一种愈合能力较差的复杂组织。目前基于间充质基质细胞(MSC)的软骨修复方法往往不尽人意,因为缺乏能驱动MSC向稳定成熟软骨细胞表型分化的相关分化因子。

结果

我们使用大规模转录组学方法,利用参考软骨微珠模型鉴定在软骨形成分化早期被调控的基因。我们鉴定出几个被调控的基因,并选择神经介素B(NMB)作为早期且瞬时被调控的基因之一。我们发现NMB的适时上调对软骨形成具有特异性,在成骨或脂肪形成过程中未观察到。此外,NMB表达水平与MSC的分化能力相关,其抑制导致软骨形成分化受损,表明NMB是软骨形成所必需的。我们进一步表明,NMB通过钙依赖性信号通路激活钙调神经磷酸酶活性。

结论

NMB是一种新描述的软骨诱导生物活性因子,通过调节钙信号通路和钙调神经磷酸酶活性上调关键软骨形成转录因子Sox9。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea8/8525028/cef0266da94a/13578_2021_695_Fig1_HTML.jpg

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