A single-cell atlas depicting the cellular and molecular features in human ligamental degeneration: a single cell combined spatial transcriptomics study

细胞 生物 计算生物学 病理 医学 遗传学
作者
Runze Yang,Tianhao Xu,Lei Zhang,Minghao Ge,Luke Yan,Jian Li,Weili Fu
出处
期刊:eLife [eLife Sciences Publications, Ltd.]
卷期号:12
标识
DOI:10.7554/elife.85700
摘要

Background: To systematically identify cell types in the human ligament, investigate how ligamental cell identities, functions, and interactions participated in the process of ligamental degeneration, and explore the changes of ligamental microenvironment homeostasis in the disease progression. Methods: Using single-cell RNA sequencing and spatial RNA sequencing of approximately 49356 cells, we created a comprehensive cell atlas of healthy and degenerated human anterior cruciate ligaments. We explored the variations of the cell subtypes' spatial distributions and the different processes involved in the disease progression, linked them with the ligamental degeneration process using computational analysis, and verified findings with immunohistochemical and immunofluorescent staining. Results: We identified new fibroblast subgroups that contributed to the disease, mapped out their spatial distribution in the tissue and revealed two dynamic trajectories in the process of the degenerative process. We compared the cellular interactions between different tissue states and identified important signaling pathways that may contribute to the disease. Conclusion: This cell atlas provides the molecular foundation for investigating how ligamental cell identities, biochemical functions, and interactions contributed to the ligamental degeneration process. The discoveries revealed the pathogenesis of ligamental degeneration at the single-cell and spatial level, which is characterized by extracellular matrix remodeling. Our results provide new insights into the control of ligamental degeneration and potential clues to developing novel diagnostic and therapeutic strategies. Funding: This study was funded by the National Natural Science Foundation of China (81972123, 82172508), Sichuan Science and Technology Program (2020YFH0075), Fundamental Research Funds for the Central Universities (2015SCU04A40), Chengdu Science and Technology Bureau Project (2019-YF05-00090-SN), and 1.3.5 Project for Disciplines of Excellence of West China Hospital Sichuan University (ZYJC21030, ZY2017301).
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
四月一日完成签到,获得积分10
刚刚
Cell完成签到 ,获得积分10
刚刚
跌跌撞撞发布了新的文献求助10
1秒前
zzz完成签到,获得积分10
2秒前
在水一方应助hzf采纳,获得10
3秒前
小嘉贞完成签到,获得积分10
3秒前
lllll完成签到 ,获得积分10
3秒前
4秒前
SciGPT应助机智宛秋采纳,获得10
5秒前
知昂完成签到 ,获得积分10
5秒前
5秒前
5秒前
852应助义气青亦采纳,获得10
6秒前
JamesPei应助fouli采纳,获得10
6秒前
北辰完成签到,获得积分10
6秒前
天舞英姿完成签到,获得积分10
7秒前
善良幼枫完成签到,获得积分10
7秒前
科研通AI5应助追寻远山采纳,获得30
7秒前
7秒前
Akim应助阳光的豁采纳,获得10
8秒前
我是老大应助李洛洛采纳,获得10
8秒前
王王完成签到,获得积分10
10秒前
科研通AI2S应助陈峰琦采纳,获得10
10秒前
怕黑海冬完成签到,获得积分10
10秒前
10秒前
瑶625发布了新的文献求助10
10秒前
大个应助明天不熬夜采纳,获得10
11秒前
地塞米松磷酸钠完成签到,获得积分10
11秒前
juejue333完成签到,获得积分10
12秒前
12秒前
高高雨寒完成签到 ,获得积分10
13秒前
风趣安青完成签到 ,获得积分10
13秒前
14秒前
14秒前
研友_VZG7GZ应助小吕采纳,获得10
14秒前
14秒前
铁男完成签到,获得积分10
15秒前
霍笑白完成签到,获得积分10
15秒前
15秒前
CipherSage应助幸福鱼采纳,获得10
16秒前
高分求助中
Genetics: From Genes to Genomes 3000
Continuum thermodynamics and material modelling 3000
Production Logging: Theoretical and Interpretive Elements 2500
Healthcare Finance: Modern Financial Analysis for Accelerating Biomedical Innovation 2000
Applications of Emerging Nanomaterials and Nanotechnology 1111
Les Mantodea de Guyane Insecta, Polyneoptera 1000
Theory of Block Polymer Self-Assembly 750
热门求助领域 (近24小时)
化学 医学 材料科学 生物 工程类 有机化学 生物化学 纳米技术 内科学 物理 化学工程 计算机科学 复合材料 基因 遗传学 物理化学 催化作用 细胞生物学 免疫学 电极
热门帖子
关注 科研通微信公众号,转发送积分 3475144
求助须知:如何正确求助?哪些是违规求助? 3067108
关于积分的说明 9102651
捐赠科研通 2758525
什么是DOI,文献DOI怎么找? 1513685
邀请新用户注册赠送积分活动 699763
科研通“疑难数据库(出版商)”最低求助积分说明 699119