影响大脑实质的进行性罗赛-多夫曼病的单细胞分析:病例报告。

IF 6.2 2区 医学 Q1 NEUROSCIENCES
Guo-Hao Huang, Guo-Long Liu, De-Zhi Huang, Xin-Wei Diao, Sheng-Qing Lv
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引用次数: 0

摘要

神经性罗赛-多夫曼病(RDD)是一种罕见的非朗格汉斯细胞组织细胞增生症,会影响中枢神经系统。大多数神经性罗赛-多夫曼病生长方式类似脑膜瘤,边界清晰,可以完全切除。然而,少数 RDDs 具有侵袭性和侵袭性,由于其分子机制尚不清楚,因此没有有效的治疗方案。在此,我们报告了一例致命的糖皮质激素耐药神经性 RDD,并通过单细胞 RNA 测序探讨了其可能的致病机制。首先,我们在活检样本中发现了两个不同但进化相关的组织细胞亚群(C1Q+ 和 SPP1+ 组织细胞)。KRAS信号通路中的基因表达上调,表明KRAS突变产生了功能增益。C1Q+ 和 SPP1+ 组织细胞高度分化并停滞在 G1 期,这排除了 RDD 是一种淋巴组织增生性疾病的可能性。其次,尽管C1Q+组织细胞是RDD的主要细胞类型,但SPP1+组织细胞高度表达多种严重炎症相关因子和侵袭因子,如WNT5A、IL-6和MMP12,这表明SPP1+组织细胞在推动该疾病进展方面起着核心作用。第三,研究发现少突胶质细胞是通过 MIF 启动 RDD 的主要细胞类型,并可通过 MDK 和 PTN 信号通路抵抗糖皮质激素治疗。总之,在本病例中,我们报告了一种罕见的神经系统 RDD 表现,并对进行性神经系统 RDD 的发病机制提供了新的见解。这项研究还将为开发针对这种复杂疾病的精准疗法提供证据。
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 of a progressive Rosai-Dorfman disease affecting the cerebral parenchyma: a case report.

Neurologic Rosai-Dorfman disease (RDD) is a rare type of non-Langerhans cell histiocytosis that affects the central nervous system. Most neurologic RDDs grow like meningiomas, have clear boundaries, and can be completely resected. However, a few RDDs are invasive and aggressive, and no effective treatment options are available because the molecular mechanisms involved remain unknown. Here, we report a case of deadly and glucocorticoid-resistant neurologic RDD and explore its possible pathogenic mechanisms via single-cell RNA sequencing. First, we identified two distinct but evolutionarily related histiocyte subpopulations (the C1Q+ and SPP1+ histiocytes) that accumulated in the biopsy sample. The expression of genes in the KRAS signaling pathway was upregulated, indicating gain-of-function of KRAS mutations. The C1Q+ and SPP1+ histiocytes were highly differentiated and arrested in the G1 phase, excluding the idea that RDD is a lympho-histio-proliferative disorder. Second, although C1Q+ histiocytes were the primary RDD cell type, SPP1+ histiocytes highly expressed several severe inflammation-related and invasive factors, such as WNT5A, IL-6, and MMP12, suggesting that SPP1+ histiocytes plays a central role in driving the progression of this disease. Third, oligodendrocytes were found to be the prominent cell type that initiates RDD via MIF and may resist glucocorticoid treatment via the MDK and PTN signaling pathways. In summary, in this case, we report a rare presentation of neurologic RDD and provided new insight into the pathogenic mechanisms of progressive neurologic RDD. This study will also offer evidence for developing precision therapies targeting this complex disease.

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来源期刊
Acta Neuropathologica Communications
Acta Neuropathologica Communications Medicine-Pathology and Forensic Medicine
CiteScore
11.20
自引率
2.80%
发文量
162
审稿时长
8 weeks
期刊介绍: "Acta Neuropathologica Communications (ANC)" is a peer-reviewed journal that specializes in the rapid publication of research articles focused on the mechanisms underlying neurological diseases. The journal emphasizes the use of molecular, cellular, and morphological techniques applied to experimental or human tissues to investigate the pathogenesis of neurological disorders. ANC is committed to a fast-track publication process, aiming to publish accepted manuscripts within two months of submission. This expedited timeline is designed to ensure that the latest findings in neuroscience and pathology are disseminated quickly to the scientific community, fostering rapid advancements in the field of neurology and neuroscience. The journal's focus on cutting-edge research and its swift publication schedule make it a valuable resource for researchers, clinicians, and other professionals interested in the study and treatment of neurological conditions.
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