单细胞分析结合机器学习阐明椎间盘退变中髓核细胞凋亡的机制和治疗干预。

IF 3.4 3区 医学 Q1 ORTHOPEDICS
JOR Spine Pub Date : 2025-01-20 DOI:10.1002/jsp2.70036
Chao Song, Xiaofei Wu, Chaoqi Chen, Baoxin Shen, Yongliang Mei, Qian Yan, Feng Jiang, Feng Chen, Fei Liu
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引用次数: 0

摘要

背景:椎间盘退变(IVDD)的分子机制尚不清楚。说到治疗汤剂,中药是有效的。尤其是独活(白芷)可能特别有帮助。目的:鉴定髓核细胞亚群和免疫细胞,阐明IVDD的治疗机制,为诊断和治疗提供建议。方法:IVDD靶点来自基因卡和生物数据库的芯片数据。为了找到IVDD的关键基因和生物学途径,使用了多种机器学习技术。单细胞分析显示,IVDD与npc亚群相关,免疫细胞AI鉴定了免疫浸润。为了验证独活活性影响IVDD的分子途径,我们采用了网络药理学和分子对接的方法。结果:IVDD的发生与TP53、JUN、PTEN、IL1B、ERBB2、MAPK8、CASP9、PTK2等关键基因有关。参与这一过程的主要分子机制包括免疫反应、炎症因子表达、细胞对机械刺激的反应和鼻咽癌细胞凋亡。免疫细胞AI发现CD4 naïve、B细胞、单核细胞、NK和巨噬细胞浸润与IVDD的发生相关。与IVDD相关的NPC亚型,即fibroNPCs、粘附NPC、调节性NPC、稳态NPC和肥厚性软骨细胞样NPC (HT-CL NPC),是单细胞定位的主题。我们还发现蛇床子素、Columbianadin和Bergapten是Dohuo的主要血液进入成分,它们可能通过调节凋亡靶点CASP9、MAPK8、PTGS1和PARP1发挥作用。结论:IVDD中存在的NPC亚群包括HT-CL NPC、fibroNPCs、粘附NPC、调节性NPC和稳态NPC。此外,多种免疫细胞的浸润,特别是单核细胞和巨噬细胞,对IVDD的进展有重要影响。毒活的主要成分蛇床子素、Columbianadin和Bergapten通过控制npc的死亡来吸收IVDD。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Single-Cell Analysis Integrated With Machine Learning Elucidates the Mechanisms of Nucleus Pulposus Cells Apoptosis in Intervertebral Disc Degeneration and Therapeutic Interventions

Single-Cell Analysis Integrated With Machine Learning Elucidates the Mechanisms of Nucleus Pulposus Cells Apoptosis in Intervertebral Disc Degeneration and Therapeutic Interventions

Background

The molecular of intervertebral disc degeneration (IVDD) is still unclear. When it comes to treating decoction, traditional Chinese medicine is effective. In particular, the Duhuo (Radix Angelicae Biseratae) may be particularly helpful.

Purpose

To identify nucleus pulposus cells (NPCs) subpopulations and immune cells and clarify the mechanism of IVDD therapy, offering recommendations for diagnosis and treatment.

Methods

IVDD targets from the Genecards and microarray data from biological databases. To find the key genes and biological pathways underlying IVDD, multiple machine learning techniques were used. IVDD is associated with subpopulations of NPCs as revealed by single-cell analysis, and immunological infiltration was identified by Immune Cell AI. To validate the molecular pathways by which Duhuo activity affects IVDD, network pharmacology and molecular docking were employed.

Results

The process of IVDD is linked to key genes like TP53, JUN, PTEN, IL1B, ERBB2, MAPK8, CASP9, PTK2, etc. The main molecular mechanisms involved in this process are immune responses, inflammatory factors expression, cellular responses to mechanical stimuli, and NPC apoptosis. Immune Cell AI discovered a correlation between CD4 naïve, B cell, monocyte, NK, and macrophage infiltration with the development of IVDD. The NPC subtypes associated with IVDD, namely fibroNPCs, adhesion NPCs, regulatory NPCs, homeostatic NPCs, and hypertrophic chondrocyte-like NPCs (HT-CL NPCs), were the subject of single-cell mapping. We also found that Osthole, Columbianadin, and Bergapten, the principal blood entry components of Dohuo, may have a role by modulating CASP9, MAPK8, PTGS1, and PARP1, the targets of apoptosis.

Conclusion

The NPC subpopulations that exist in IVDD are HT-CL NPCs, fibroNPCs, adhesion NPCs, regulatory NPCs, and homeostatic NPCs. Furthermore, a variety of immune cell infiltrates, particularly monocyte and macrophage, have a significant impact on the advancement of IVDD. Osthole, Columbianadin, and Bergapten, the principal components of Duhuo, absorb IVDD via controlling the death of NPCs.

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JOR Spine
JOR Spine ORTHOPEDICS-
CiteScore
6.40
自引率
18.90%
发文量
42
审稿时长
10 weeks
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