Activatable Fluorescence Imaging of Macrophages in Cerebral Aneurysms Using Iron Oxide Nanoparticles Conjugated With Indocyanine Green

被引:5
作者
Ikeda, Hiroyuki [1 ,2 ]
Ishii, Akira [1 ]
Sano, Kohei [2 ,3 ]
Chihara, Hideo [1 ]
Arai, Daisuke [1 ]
Abekura, Yu [1 ]
Nishi, Hidehisa [1 ]
Ono, Masahiro [2 ]
Saji, Hideo [2 ]
Miyamoto, Susumu [1 ]
机构
[1] Kyoto Univ, Dept Neurosurg, Grad Sch Med, Kyoto, Japan
[2] Kyoto Univ, Grad Sch Pharmaceut Sci, Dept Pathofunct Bioanal, Kyoto, Japan
[3] Kobe Pharmaceut Univ, Lab Biophys Chem, Kobe, Hyogo, Japan
基金
日本学术振兴会;
关键词
macrophage; inflammation; cerebral aneurysm; iron oxide nanoparticles; fluorescent imaging; indocyanine green; KAPPA-B; FERUMOXYTOL; PROGRESSION; HEMODYNAMICS; WALL;
D O I
10.3389/fnins.2020.00370
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background and Purpose Chronic inflammation is involved in the formation and enlargement of cerebral aneurysms (CAs), with macrophages playing a key role in the process. The present study evaluated visualization of macrophages present in CAs using an activatable fluorescent probe (IONP-ICG) comprising an iron oxide nanoparticles (IONPs) conjugated with indocyanine green (ICG). Methods IONP-ICG was intravenously administered to 15-week-old CA model rats (n = 8), and ex vivo near-infrared fluorescence (NIRF) imaging and histological assessment of exposed CAs and cerebral arteries were performed 48 h later. Similar evaluations were performed in the control group, which included CA model rats given IONPs or ICG (n = 8 each). Results ICG-derived NIRF signals were detected in three IONP-ICG group rats but not in IONP or ICG control groups. Among the three rats that exhibited signals, NIRF signal accumulation was observed in the CA of two rats and at the site of hemodynamic stress in the left posterior cerebral artery in one rat. Histologically, NIRF signals correlated strongly with macrophage localization. A total of 13 CAs formed in the IONP-ICG group. The number of macrophages in the CA wall was significantly greater in the two CAs that exhibited NIRF signals compared to the remaining 11 CAs that did not (P = 0.037). Moreover, all 11 CAs that did not exhibit NIRF signals were iron-negative, while the two CAs that exhibited NIRF signals were both iron-positive (P = 0.013). Conclusion NIRF imaging using an activatable IONP-ICG probe is feasible for detecting the macrophage-rich regions in CAs and the cerebral artery wall, which is considered an early lesion in the process of CA formation.
引用
收藏
页数:10
相关论文
共 30 条
  • [11] A target cell-specific activatable fluorescence probe for in vivo molecular imaging of cancer based on a self-quenched avidin-rhodamine conjugate
    Hama, Yukihiro
    Urano, Yasuteru
    Koyama, Yoshinori
    Kamiya, Mako
    Bernardo, Marcelino
    Paik, Ronald S.
    Shin, In Soo
    Paik, Chang H.
    Choyke, Peter L.
    Kobayashi, Hisataka
    [J]. CANCER RESEARCH, 2007, 67 (06) : 2791 - 2799
  • [12] Evidence That Acetylsalicylic Acid Attenuates Inflammation in the Walls of Human Cerebral Aneurysms: Preliminary Results
    Hasan, David M.
    Chalouhi, Nohra
    Jabbour, Pascal
    Dumont, Aaron S.
    Kung, David K.
    Magnotta, Vincent A.
    Young, William L.
    Hashimoto, Tomoki
    Winn, H. Richard
    Heistad, Donald
    [J]. JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2013, 2 (01): : e000019
  • [13] Macrophage Imaging Within Human Cerebral Aneurysms Wall Using Ferumoxytol-Enhanced MRI: A Pilot Study
    Hasan, David M.
    Mahaney, Kelly B.
    Magnotta, Vincent A.
    Kung, David K.
    Lawton, Michael T.
    Hashimoto, Tomoki
    Winn, H. Richard
    Saloner, David
    Martin, Alastair
    Gahramanov, Seymur
    Dosa, Edit
    Neuwelt, Edward
    Young, William L.
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2012, 32 (04) : 1032 - 1038
  • [14] HASHIMOTO N, 1980, SURG NEUROL, V13, P41
  • [15] Treatment of Recurrent Intracranial Aneurysms After Clipping: A Report of 23 Cases and a Review of the Literature
    Hokari, Masaaki
    Kazumara, Ken
    Nakayama, Naoki
    Ushikoshi, Satoshi
    Sugiyama, Taku
    Asaoka, Katsunori
    Uchida, Kazuki
    Shimbo, Daisuke
    Itamoto, Koji
    Yokoyama, Yuka
    Isobe, Masanori
    Imai, Tetsuaki
    Osanai, Toshiya
    Houkin, Kiyohiro
    [J]. WORLD NEUROSURGERY, 2016, 92 : 434 - 444
  • [16] Activatable fluorescence imaging of macrophages in atherosclerotic plaques using iron oxide nanoparticles conjugated with indocyanine green
    Ikeda, Hiroyuki
    Ishii, Akira
    Sano, Kohei
    Chihara, Hideo
    Arai, Daisuke
    Abekura, Yu
    Nishi, Hidehisa
    Ono, Masahiro
    Saji, Hideo
    Miyamoto, Susumu
    [J]. ATHEROSCLEROSIS, 2018, 275 : 1 - 10
  • [17] Dipeptidyl Peptidase-4 Inhibitor Anagliptin Prevents Intracranial Aneurysm Growth by Suppressing Macrophage Infiltration and Activation
    Ikedo, Taichi
    Minami, Manabu
    Kataoka, Hiroharu
    Hayashi, Kosuke
    Nagata, Manabu
    Fujikawa, Risako
    Higuchi, Sei
    Yasui, Mika
    Aoki, Tomohiro
    Fukuda, Miyuki
    Yokode, Masayuki
    Miyamoto, Susumu
    [J]. JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2017, 6 (06):
  • [18] Multimodality Imaging Reveals a Gradual Increase in Matrix Metalloproteinase Activity at Aneurysmal Lesions in Live Fibulin-4 Mice
    Kaijzel, Eric L.
    van Heijningen, Paula M.
    Wielopolski, Piotr A.
    Vermeij, Marcel
    Koning, Gerben A.
    van Cappellen, Wiggert A.
    Que, Ivo
    Chan, Alan
    Dijkstra, Jouke
    Ramnath, Natasja W. M.
    Hawinkels, Lukas J. A. C.
    Bernsen, Monique R.
    Lowik, Clemens W. G. M.
    Essers, Jeroen
    [J]. CIRCULATION-CARDIOVASCULAR IMAGING, 2010, 3 (05) : 567 - 577
  • [19] Critical Roles of Macrophages in the Formation of Intracranial Aneurysm
    Kanematsu, Yasuhisa
    Kanematsu, Miyuki
    Kurihara, Chie
    Tada, Yoshiteru
    Tsou, Tsung-Ling
    van Rooijen, Nico
    Lawton, Michael T.
    Young, William L.
    Liang, Elena I.
    Nuki, Yoshitsugu
    Hashimoto, Tomoki
    [J]. STROKE, 2011, 42 (01) : 173 - 178
  • [20] Molecular Mechanisms of the Formation and Progression of Intracranial Aneurysms
    Kataoka, Hiroharu
    [J]. NEUROLOGIA MEDICO-CHIRURGICA, 2015, 55 (03) : 214 - 229