• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

趋化信号传导、小胶质细胞与阿尔茨海默病老年斑:存在关联吗?

Chemotactic signaling, microglia, and Alzheimer's disease senile plaques: is there a connection?

作者信息

Luca Magdalena, Chavez-Ross Alexandra, Edelstein-Keshet Leah, Mogilner Alex

机构信息

Massachusetts College of Pharmacy and Health Sciences, School of Arts and Sciences, 179 Longwood Avenue, Boston, MA 021 15-5896, USA.

出版信息

Bull Math Biol. 2003 Jul;65(4):693-730. doi: 10.1016/S0092-8240(03)00030-2.

DOI:10.1016/S0092-8240(03)00030-2
PMID:12875339
Abstract

Chemotactic cells known as microglia are involved in the inflammation associated with pathology in Alzheimer's disease (AD). We investigate conditions that lead to aggregation of microglia and formation of local accumulations of chemicals observed in AD senile plaques. We develop a model for chemotaxis in response to a combination of chemoattractant and chemorepellent signaling chemicals. Linear stability analysis and numerical simulations of the model predict that periodic patterns in cell and chemical distributions can evolve under local attraction, long-ranged repulsion, and other constraints on concentrations and diffusion coefficients of the chemotactic signals. Using biological parameters from the literature, we compare and discuss the applicability of this model to actual processes in AD.

摘要

被称为小胶质细胞的趋化细胞参与了与阿尔茨海默病(AD)病理相关的炎症反应。我们研究了导致小胶质细胞聚集以及在AD老年斑中观察到的化学物质局部积累形成的条件。我们建立了一个响应趋化因子和化学排斥信号化学物质组合的趋化模型。该模型的线性稳定性分析和数值模拟预测,在局部吸引、长程排斥以及对趋化信号浓度和扩散系数的其他限制条件下,细胞和化学物质分布的周期性模式可能会演变。利用文献中的生物学参数,我们比较并讨论了该模型对AD实际过程的适用性。

相似文献

1
Chemotactic signaling, microglia, and Alzheimer's disease senile plaques: is there a connection?趋化信号传导、小胶质细胞与阿尔茨海默病老年斑:存在关联吗?
Bull Math Biol. 2003 Jul;65(4):693-730. doi: 10.1016/S0092-8240(03)00030-2.
2
Hematopoietic prostaglandin D synthase and DP1 receptor are selectively upregulated in microglia and astrocytes within senile plaques from human patients and in a mouse model of Alzheimer disease.造血前列腺素D合成酶和DP1受体在人类患者老年斑内的小胶质细胞和星形胶质细胞中以及阿尔茨海默病小鼠模型中选择性上调。
J Neuropathol Exp Neurol. 2007 Jun;66(6):469-80. doi: 10.1097/01.jnen.0000240472.43038.27.
3
Rat microglia exhibit increased density on Alzheimer's plaques in vitro.大鼠小胶质细胞在体外对阿尔茨海默病斑块的密度增加。
Exp Neurol. 1998 Jan;149(1):42-50. doi: 10.1006/exnr.1997.6678.
4
Multiple sclerosis and Alzheimer's disease.多发性硬化症和阿尔茨海默病。
Ann Neurol. 2008 Feb;63(2):174-83. doi: 10.1002/ana.21240.
5
Bone marrow-derived microglia play a critical role in restricting senile plaque formation in Alzheimer's disease.骨髓来源的小胶质细胞在限制阿尔茨海默病中淀粉样斑块形成方面发挥着关键作用。
Neuron. 2006 Feb 16;49(4):489-502. doi: 10.1016/j.neuron.2006.01.022.
6
Contribution of glial cells to the development of amyloid plaques in Alzheimer's disease.胶质细胞在阿尔茨海默病淀粉样斑块形成中的作用。
Neurobiol Aging. 2004 May-Jun;25(5):663-74. doi: 10.1016/j.neurobiolaging.2004.01.007.
7
Apolipoprotein D is a component of compact but not diffuse amyloid-beta plaques in Alzheimer's disease temporal cortex.载脂蛋白D是阿尔茨海默病颞叶皮质中致密型而非弥漫型β淀粉样蛋白斑块的一个组成部分。
Neurobiol Dis. 2005 Nov;20(2):574-82. doi: 10.1016/j.nbd.2005.04.012.
8
The microglial phagocytic role with specific plaque types in the Alzheimer disease brain.小胶质细胞在阿尔茨海默病大脑中对特定斑块类型的吞噬作用。
Neurobiol Aging. 2004 May-Jun;25(5):675-83. doi: 10.1016/j.neurobiolaging.2003.12.026.
9
Regression stage senile plaques in the natural course of Alzheimer's disease.阿尔茨海默病自然病程中的消退期老年斑
Neuropathol Appl Neurobiol. 2006 Oct;32(5):539-56. doi: 10.1111/j.1365-2990.2006.00767.x.
10
Progranulin expression correlates with dense-core amyloid plaque burden in Alzheimer disease mouse models.在阿尔茨海默病小鼠模型中,前颗粒蛋白表达与致密核心淀粉样斑块负荷相关。
J Pathol. 2009 Oct;219(2):173-81. doi: 10.1002/path.2580.

引用本文的文献

1
A Keller-Segel model for C elegans L1 aggregation.一个用于 C. elegans L1 聚集的 Keller-Segel 模型。
PLoS Comput Biol. 2021 Jul 29;17(7):e1009231. doi: 10.1371/journal.pcbi.1009231. eCollection 2021 Jul.
2
Mathematical Modeling of Protein Misfolding Mechanisms in Neurological Diseases: A Historical Overview.神经疾病中蛋白质错误折叠机制的数学建模:历史概述
Front Neurol. 2018 Feb 2;9:37. doi: 10.3389/fneur.2018.00037. eCollection 2018.
3
Effect of cyto/chemokine degradation in effective intercellular communication distances.
细胞因子/趋化因子降解对有效细胞间通讯距离的影响。
Physica A. 2017 Feb 15;468:244-251. doi: 10.1016/j.physa.2016.10.098. Epub 2016 Nov 11.
4
The Impact of Mathematical Modeling in Understanding the Mechanisms Underlying Neurodegeneration: Evolving Dimensions and Future Directions.数学建模在理解神经退行性变潜在机制中的作用:不断演变的维度与未来方向
CPT Pharmacometrics Syst Pharmacol. 2017 Feb;6(2):73-86. doi: 10.1002/psp4.12155. Epub 2017 Jan 7.
5
Demyelination patterns in a mathematical model of multiple sclerosis.多发性硬化症数学模型中的脱髓鞘模式
J Math Biol. 2017 Aug;75(2):373-417. doi: 10.1007/s00285-016-1087-0. Epub 2016 Dec 30.
6
Modeling the Role of the Glymphatic Pathway and Cerebral Blood Vessel Properties in Alzheimer's Disease Pathogenesis.模拟类淋巴途径和脑血管特性在阿尔茨海默病发病机制中的作用
PLoS One. 2015 Oct 8;10(10):e0139574. doi: 10.1371/journal.pone.0139574. eCollection 2015.
7
Mathematical modeling for the pathogenesis of Alzheimer's disease.阿尔茨海默病发病机制的数学建模。
PLoS One. 2010 Dec 14;5(12):e15176. doi: 10.1371/journal.pone.0015176.
8
A user's guide to PDE models for chemotaxis.趋化作用的偏微分方程(PDE)模型用户指南
J Math Biol. 2009 Jan;58(1-2):183-217. doi: 10.1007/s00285-008-0201-3. Epub 2008 Jul 15.