High-resolution architecture of human epiphysis formation

软骨内骨化 软骨细胞 软骨 骨骺 骨化 骨化中心 软骨发生 解剖 硫氧化物9 细胞生物学 生物 基因表达 遗传学 基因
作者
Heng Sun,Ya Wen,Weiliang Wu,Tian Qin,Chengrui An,Chunmei Fan,Yishan Chen,Junfeng Ji,Ting Gang Chew,Jiansong Chen,Hongwei Ouyang
标识
DOI:10.1101/2020.10.13.337733
摘要

Summary Human limb skeletal system consists of both bone and cartilage which originated from fetal cartilage. However, the roadmap of chondrocyte divergent differentiation to bone and articular cartilage has yet to be established. Epiphysis possesses articular cartilage, growth plate and the secondary ossification center (SOC), making it an ideal model to uncover the trajectory of chondrocyte divergent differentiation. Here, we mapped differentiation trajectory of human chondrocyte during postnatal finger epiphysis development by using single-cell RNA sequencing. Our results uncovered that chondroprogenitors have two differentiation pathways to hypertrophic chondrocytes during ossification, and one pathway to articular chondrocytes for formation of cartilages. Interestingly, we found that, as an addition to the known typical endochondral ossification path from resting, proliferative to hypertrophic chondrocytes, there was a bypass by which chondroprogenitors differentiate into hypertrophic chondrocytes without proliferative stage. Furthermore, our results revealed two new chondrocyte subpopulations (bypass chondrocytes as it appeared in the ossification bypass, and ID1 + chondroblasts in articular chondrocyte path) during postnatal epiphysis development in addition to six well-known subpopulations. Overall, our study provides a comprehensive roadmap of chondrocyte differentiation in human epiphysis thereby expanding the knowledge of bone and articular cartilage, which could be utilized to design biotherapeutics for bone and articular cartilage regeneration.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
2秒前
点击完成签到,获得积分10
2秒前
蔡万润完成签到 ,获得积分10
3秒前
Tysonqu发布了新的文献求助10
4秒前
cdercder应助斯巴达采纳,获得10
4秒前
NexusExplorer应助淡然钢铁侠采纳,获得10
5秒前
小甄同学发布了新的文献求助10
5秒前
6秒前
7秒前
JamesPei应助清水小镇采纳,获得30
7秒前
852应助leo_zjm采纳,获得10
8秒前
8秒前
8秒前
8秒前
2032jia完成签到,获得积分10
8秒前
爱吃无核瓜子完成签到,获得积分10
9秒前
9秒前
霍明轩完成签到 ,获得积分10
11秒前
胡元军完成签到,获得积分20
11秒前
SamYang发布了新的文献求助10
11秒前
文艺紫菜发布了新的文献求助10
11秒前
11秒前
1111完成签到,获得积分10
12秒前
CodeCraft应助xxy采纳,获得10
12秒前
12秒前
13秒前
13秒前
楠瓜瓜完成签到,获得积分10
13秒前
13秒前
ProfLi完成签到,获得积分10
14秒前
纯真的醉柳完成签到,获得积分10
14秒前
15秒前
15秒前
大个应助小菜花采纳,获得10
16秒前
16秒前
酷波er应助TangSEU采纳,获得10
16秒前
现实的如之完成签到 ,获得积分10
16秒前
贪玩擎汉发布了新的文献求助10
17秒前
lv完成签到,获得积分10
17秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Prompt Engineering for Clinicians: Harnessing AI in Everyday Medical Practice 600
University Physics for the Life Sciences 500
REAL-WORLD EFFICACY AND GENOMIC LANDSCAPE OF POLATUZUMA VEDOTIN-BASED FIRST-LINE THERAPY IN DIFFUSE LARGE B-CELL LYMPHOMA: A FOCUS ON TP53 MUTATIONS AND TREATMENT RESPONSE 500
Handbook of Luminescence Dating 500
Safety Pharmacology 500
《KNN基无铅压电陶瓷电学性能优化与物理机理研究》 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 计算机科学 化学工程 生物化学 物理 内科学 复合材料 催化作用 光电子学 物理化学 电极 细胞生物学 基因 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6954499
求助须知:如何正确求助?哪些是违规求助? 8638288
关于积分的说明 18318668
捐赠科研通 6398895
什么是DOI,文献DOI怎么找? 3083309
关于科研通互助平台的介绍 2129412
邀请新用户注册赠送积分活动 2060065