Suppr超能文献

角膜白细胞的活体多光子显微镜动力学研究。

Kinetics of corneal leukocytes by intravital multiphoton microscopy.

机构信息

Center for Translational Ocular Immunology, Tufts Medical Center, Tufts University School of Medicine, Tufts University, Boston, Massachusetts, USA.

Department of Ophthalmology, Tufts Medical Center, Tufts University School of Medicine, Tufts University, Boston, Massachusetts, USA.

出版信息

FASEB J. 2019 Feb;33(2):2199-2211. doi: 10.1096/fj.201800684RR. Epub 2018 Sep 18.

Abstract

Corneal immune privilege is integral in maintaining the clear avascular window to the foreign world. The presence of distinct populations of corneal leukocytes (CLs) in the normal cornea has been firmly established. However, their precise function and kinetics remain, as of yet, unclear. Through intravital multiphoton microscopy (IV-MPM), allowing the means to accumulate critical spatial and temporal cellular information, we provide details for long-term investigation of CL morphology and kinetics under steady state and following inflammation. Significant alterations in size and morphology of corneal CD11c dendritic cells (DCs) were noted following acute sterile inflammation, including cell volume (4364.4 ± 489.6 vs. 1787.6 ± 111.0 μm, P < 0.001) and sphericity (0.82 ± 0.01 vs. 0.42 ± 0.02, P < 0.001) compared with steady state. Furthermore, IV-MPM analyses revealed alterations in both the CD11c DC and major histocompatibility complex class II (MHC)-II mature antigen-presenting cell population kinetics during inflammation, including track displacement length (CD11c: 16.57 ± 1.41 vs. 4.64 ± 0.56 μm, P < 0.001; MHC-II: 9.03 ± 0.37 vs. 4.09 ± 0.39, P < 0.001) and velocity (CD11c: 1.91 ± 0.07 μm/min vs. 1.73 ± 0.1302 μm/min; MHC-II: 2.97 ± 0.07 vs. 1.62 ± 0.08, P < 0.001) compared with steady state. Our results reveal in vivo evidence of sessile CL populations exhibiting dendritic morphology under steady state and increased velocity of spherical leukocytes following inflammation. IV-MPM represents a powerful tool to study leukocytes in corneal diseases in context.-Seyed-Razavi, Y., Lopez, M. J., Mantopoulos, D., Zheng, L., Massberg, S., Sendra, V. G., Harris, D. L., Hamrah, P. Kinetics of corneal leukocytes by intravital multiphoton microscopy.

摘要

角膜免疫特权对于维持对外界透明无血管的窗口至关重要。正常角膜中存在不同群体的角膜白细胞(CLs)已得到明确证实。然而,它们的确切功能和动力学仍然不清楚。通过活体多光子显微镜(IV-MPM),我们可以积累关键的时空细胞信息,为在稳态和炎症后长期研究 CL 形态和动力学提供详细信息。在急性无菌性炎症后,角膜 CD11c 树突状细胞(DCs)的大小和形态发生了显著变化,包括细胞体积(4364.4 ± 489.6 与 1787.6 ± 111.0 μm,P < 0.001)和球形度(0.82 ± 0.01 与 0.42 ± 0.02,P < 0.001)与稳态相比。此外,IV-MPM 分析显示,在炎症过程中,CD11c DC 和主要组织相容性复合体 II(MHC-II)成熟抗原呈递细胞群体的动力学都发生了变化,包括轨迹位移长度(CD11c:16.57 ± 1.41 与 4.64 ± 0.56 μm,P < 0.001;MHC-II:9.03 ± 0.37 与 4.09 ± 0.39,P < 0.001)和速度(CD11c:1.91 ± 0.07 μm/min 与 1.73 ± 0.1302 μm/min;MHC-II:2.97 ± 0.07 与 1.62 ± 0.08,P < 0.001)与稳态相比。我们的结果提供了活体证据,表明在稳态下,静止的 CL 群体表现出树突状形态,而在炎症后,球形白细胞的速度增加。IV-MPM 是一种强大的工具,可用于在背景下研究角膜疾病中的白细胞。-Seyed-Razavi,Y.,Lopez,M. J.,Mantopoulos,D.,Zheng,L.,Massberg,S.,Sendra,V. G.,Harris,D. L.,Hamrah,P. 通过活体多光子显微镜研究角膜白细胞的动力学。

相似文献

1
Kinetics of corneal leukocytes by intravital multiphoton microscopy.
FASEB J. 2019 Feb;33(2):2199-2211. doi: 10.1096/fj.201800684RR. Epub 2018 Sep 18.
2
Multiphoton Intravital Microscopy of Mandibular Draining Lymph Nodes: A Mouse Model to Study Corneal Immune Responses.
Front Immunol. 2020 Feb 21;11:39. doi: 10.3389/fimmu.2020.00039. eCollection 2020.
6
Alterations in corneal stromal dendritic cell phenotype and distribution in inflammation.
Arch Ophthalmol. 2003 Aug;121(8):1132-40. doi: 10.1001/archopht.121.8.1132.
7
CD34+ corneal stromal cells are bone marrow-derived and express hemopoietic stem cell markers.
Stem Cells. 2005 Apr;23(4):507-15. doi: 10.1634/stemcells.2004-0291.
9
Epifluorescence intravital microscopy of murine corneal dendritic cells.
Invest Ophthalmol Vis Sci. 2010 Apr;51(4):2101-8. doi: 10.1167/iovs.08-2213. Epub 2009 Dec 10.
10

引用本文的文献

2
JR5558 mice are a reliable model to investigate subretinal fibrosis.
Sci Rep. 2024 Aug 13;14(1):18752. doi: 10.1038/s41598-024-66068-z.
3
Posterior corneoscleral limbus: Architecture, stem cells, and clinical implications.
Prog Retin Eye Res. 2023 Sep;96:101192. doi: 10.1016/j.preteyeres.2023.101192. Epub 2023 Jun 29.
6
Immunomodulatory Role of Neuropeptides in the Cornea.
Biomedicines. 2022 Aug 16;10(8):1985. doi: 10.3390/biomedicines10081985.
10

本文引用的文献

2
Visualization of Intravital Immune Cell Dynamics After Conjunctival Surgery Using Multiphoton Microscopy.
Invest Ophthalmol Vis Sci. 2016 Mar;57(3):1207-12. doi: 10.1167/iovs.15-18507.
3
Visualizing the Behavior of HIV-Infected T Cells In Vivo Using Multiphoton Intravital Microscopy.
Methods Mol Biol. 2016;1354:189-201. doi: 10.1007/978-1-4939-3046-3_13.
4
Intravital imaging of the cellular dynamics of LysM-positive cells in a murine corneal suture model.
Br J Ophthalmol. 2016 Mar;100(3):432-5. doi: 10.1136/bjophthalmol-2015-307024. Epub 2015 Nov 16.
5
Second Harmonic Generation Imaging Analysis of Collagen Arrangement in Human Cornea.
Invest Ophthalmol Vis Sci. 2015 Aug;56(9):5622-9. doi: 10.1167/iovs.15-17129.
6
TGF-β-Dependent Dendritic Cell Chemokinesis in Murine Models of Airway Disease.
J Immunol. 2015 Aug 1;195(3):1182-90. doi: 10.4049/jimmunol.1500348. Epub 2015 Jun 24.
7
Intravital two-photon imaging of the gastrointestinal tract.
J Immunol Methods. 2015 Jun;421:73-80. doi: 10.1016/j.jim.2015.03.008. Epub 2015 Mar 20.
8
Characterization of multiphoton microscopy in the bone marrow following intravital laser osteotomy.
Biomed Opt Express. 2014 Sep 12;5(10):3578-88. doi: 10.1364/BOE.5.003578. eCollection 2014 Oct 1.
9
An MHC II-dependent activation loop between adipose tissue macrophages and CD4+ T cells controls obesity-induced inflammation.
Cell Rep. 2014 Oct 23;9(2):605-17. doi: 10.1016/j.celrep.2014.09.004. Epub 2014 Oct 9.
10
Dendritic cells, monocytes and macrophages: a unified nomenclature based on ontogeny.
Nat Rev Immunol. 2014 Aug;14(8):571-8. doi: 10.1038/nri3712. Epub 2014 Jul 18.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验