Spatiotemporal Tracking of Brain-Tumor-Associated Myeloid Cells in Vivo through Optical Coherence Tomography with Plasmonic Labeling and Speckle Modulation.
Spatiotemporal Tracking of Brain-Tumor-Associated Myeloid Cells in Vivo through Optical Coherence Tomography with Plasmonic Labeling and Speckle Modulation.
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通过具有等离子体标记和散斑调制的光学相干断层扫描对体内脑肿瘤相关骨髓细胞进行时空追踪。
DOI:
10.1021/acsnano.9b02656
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发表时间:
2019
期刊:
影响因子:
17.1
通讯作者:
delaZerda,Adam
中科院分区:
文献类型:
--
作者:
SoRelle,ElliottDaniel;Yecies,DerekWilliam;Liba,Orly;Bennett,FrederickChristian;Graef,ClausMoritz;Dutta,Rebecca;Mitra,Siddhartha;Joubert,Lydia-Marie;Cheshier,Samuel;Grant,GeraldA;delaZerda,Adam
By their nature, tumors pose a set of profound challenges to the immune system with respect to cellular recognition and response coordination. Recent research indicates that leukocyte subpopulations, especially tumor-associated macrophages (TAMs), can exert substantial influence on the efficacy of various cancer immunotherapy treatment strategies. To better study and understand the roles of TAMs in determining immunotherapeutic outcomes, significant technical challenges associated with dynamically monitoring single cells of interest in relevant live animal models of solid tumors must be overcome. However, imaging techniques with the requisite combination of spatiotemporal resolution, cell-specific contrast, and sufficient signal-to-noise at increasing depths in tissue are exceedingly limited. Here we describe a method to enable high-resolution, wide-field, longitudinal imaging of TAMs based on speckle-modulating optical coherence tomography (SM-OCT) and spectral scattering from an optimized contrast agent. The approach’s improvements to OCT detection sensitivity and noise reduction enabled high-resolution OCT-based observation of individual cells of a specific host lineage in live animals. We found that large gold nanorods (LGNRs) that exhibit a narrow-band, enhanced scattering cross-section can selectively label TAMs and activate microglia in anin vivoorthotopic murine model of glioblastoma multiforme. We demonstrated near real-time tracking of the migration of cells within these myeloid subpopulations. The intrinsic spatiotemporal resolution, imaging depth, and contrast sensitivity reported herein may facilitate detailed studies of the fundamental behaviors of TAMs and other leukocytes at the single-cell levelin vivo, including intratumoral distribution heterogeneity and roles in modulating cancer proliferation.
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影响因子:
38.3
作者:
通讯作者:
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影响因子:
3.6
作者:
Tae Shik Kim;S. Jang;Nuri Oh;Yongjoo Kim;T. Park;Jiho Park;W. Oh
通讯作者:
W. Oh
影响因子:
4
作者:
Y. Winetraub;E. SoRelle;O. Liba;A. de la Zerda
通讯作者:
Y. Winetraub;E. SoRelle;O. Liba;A. de la Zerda
影响因子:
4.4
作者:
A. L. Ford;A. Goodsall;W. Hickey;J. Sedgwick
通讯作者:
A. L. Ford;A. Goodsall;W. Hickey;J. Sedgwick
影响因子:
1.7
作者:
Ripandelli, G;Coppe, A M;Stirpe, M
通讯作者:
Stirpe, M