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首页利用HSP27抗体标记的光声纳米探针成像检测神经损伤
利用HSP27抗体标记的光声纳米探针成像检测神经损伤
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更新于2024-08-27
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"利用HSP27抗体功能化的光声纳米探针成像神经损伤" 这篇论文探讨了神经损伤早期检测的重要性和一种创新的检测方法。神经损伤的及时诊断和治疗对于恢复神经功能至关重要。在遭受压伤一周后,研究发现沿着坐骨神经全长会过度表达热休克蛋白27(HSP27)。文章提出了一种新策略,即通过将HSP27抗体连接到金纳米粒子上,然后利用这些标记的纳米探针进行光声显微镜成像来检测受伤的神经。 光声成像技术结合了光学和声学的优点,可以提供高分辨率的深度成像,特别适用于生物组织内的结构和功能成像。在这项研究中,HSP27抗体的功能化金纳米粒子被用于特异性地靶向并标记受伤的神经。这些纳米探针能够吸收光能并转化为声波信号,使得在光声显微镜下可以清晰地观察到受损的神经部位。 实验结果显示,通过注射这些纳米探针,可以在损伤发生后的3至7天内,特别是在早期阶段,有效地通过光声成像技术检测到受伤的神经。这种方法可能对临床神经损伤的早期诊断具有重大意义,因为它能够在传统影像技术可能无法识别损伤的早期阶段提供清晰的图像。 此外,该研究还强调了HSP27作为一种潜在的生物标志物在神经损伤诊断中的价值。由于HSP27在损伤后表达增加,这为开发针对特定损伤状态的靶向成像策略提供了可能性。金纳米粒子因其良好的生物相容性、稳定的光学性质以及易于化学修饰的特性,成为了理想的成像载体。 这项工作展示了新型光声纳米探针在神经损伤检测中的应用潜力,为未来开发更高效的诊断工具和治疗方法提供了新的思路。同时,这也为理解和追踪神经修复过程提供了新的成像平台,可能对未来神经科学和临床神经医学领域产生深远影响。
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Imaging of nerve injury with HSP27 antibody-
functionalized photoacoustic nanoprobes
Hongjiang Chen (陈洪江)
1
, Zhongjiang Chen (陈重江)
2
,
Jankun Xu (许建坤)
1
, and Jun Hu (胡 军)
1,2,
*
1
Department of Orthopaedics, the First Affiliated Hospital, Shantou University Medical College,
Shantou 515041, China
2
MOE Key Laboratory of Laser Life Science & Institute of Laser Life Science, College of Biophotonics,
South China Normal University, Guangzhou 510631, China
*Corresponding author: hjzkm@vip.163.com
Received May 19, 2015; accepted August 28, 2015; posted online October 16, 2015
Early detection and timely treatment of nerve injury is crucial for the repair of nerve function. One week follow-
ing a crush injury, heat shock protein 27 (HSP27) is over-expressed along the entire length of the sciatic nerve.
Herein, we present an approach to detect injured nerves by photoacoustic microscopy after labeling the injured
nerve with HSP27 antibody-conjugated gold nanoparticles. The studies reveal that nanoprobe administration
enabled the detection of injured nerves by photoacoustic microscopy, especially during the early stages within
3–7 days post injury. In conclusion, photoacoustic microscopy combined with antibody-conjugated nanopar-
ticles holds potential for the early detection of nerve injury.
OCIS codes: 170.0170, 170.3880, 170.5120.
doi: 10.3788/COL201513.111701.
Evidence suggests that injured nerves can achieve better
functional recovery when treated in a timely manner
[1]
.
Therefore, early diagnosis and appropriate treatment is
very important in cases of nerve injury and would likely
lead to better functional restoration. Electromyography
(EMG) is the only approach that can detect injured motor
or sensory nerves. However, EMG is invasive and only
detects abnormalities at approximately 14–21 days after
the injury occurred
[2,3]
. Since tissue and nerves possess
early the same parameters of density and acoustic imped-
ance, conventional methods, such as ultrasound imaging,
X-rays, computed tomography (CT), and magnetic reso-
nance imaging (MRI), cannot provide high contrast imag-
ing sufficient for identifying injured nerves in situ
[2,4,5]
.
Therefore, a novel and more effective technology for the
early detection of nerve injury is urgently needed.
Advances in nanotechnology have identified promising
candidates that are more suitable for biological and
biomedical applications over a wide variety of disorders.
Nanoparticles (NPs) with unique properties such as small
particle size, novel physicochemical properties, and easy
surface modification are widely used for biomedical pur-
poses
[6,7]
. Targeting ligands, imaging labels, and therapeu -
tic drugs could all be integrated with contrast reagents as
a promising approach for targeted molecular imaging and
therapy
[8,9]
. Due to the photoacoustic effect, photoacoustic
microscopy is a noninvasive imaging modality with high
resolution and high contrast
[10–13]
. It has been successfully
applied to several biomedical applications for obtaining
structural and functional information, including the
detection of hemoglobin oxygen saturation and carboxy-
hemoglobin saturation, monitoring of vascular damage
during pho todynamic therapy treatment of tumors,
noninvasive monitoring of tr aumatic brain injury, and
post-traumatic rehabilitation
[14–17]
. Previous studies have
shown that heat shock protein 27 (HSP27) in peripheral
nerves can protect injured cells by preventing oxidative
stress
[18]
and resisting heat shock
[19]
. Costigan et al. found
that HSP27 was upregulated by 9-foldin the ipsilateral
dorsal root gang lion (DRG) 48 h after axotomy of the sci-
atic nerve
[20]
. Hirata et al. also found that HSP27 localiza-
tion extended from the proximal to the distal part of the
axon and propagated through the entire nerve within one
week after the surgery
[21]
. Therefore, due to the dramatic
upregulation of HSP27 in injured neurons, we hypoth-
esized that HSP27 could act as an effective marker for
early nerve injury. Four-week-old Sprague–Dawley (SD)
rats (male) weighing 80–100 g were used in the experi-
ments. The rats were placed under general anesthesia with
sodium pentobarbital (200 mg∕kg, i.p.) and then the left
sciatic nerve of the rat was crushed at the middle of the
femur for 30 s with Jeweler’s force ps. Control animals
received the same surgical procedure but without crushing
the nerve. Neurons were cultured according to the method
previously described
[20]
. All procedures followed the rules
of the National Animal Protection of China.
A diagram of the photoacoustic microscopy system is
presented in Fig.
1. Briefly, a tunable pulsed laser source
(Vibrant B 532I, Opotek, USA) with wavelengths of 532
and 680–960 nm, a pulse width of 10 ns, and a pulse rep-
etition rate of 10 Hz, was used to provide optical illumi-
nation. The laser beam was focused by an objective lens
through a small hole in the center of the hollow sensor
and a photodiode was used to monitor and calibrate the
beam intensity and stability. The cylindrical lens and the
position sensor device (PSD) acted as an autofocusing
COL 13(11), 111701(2015) CHINESE OPTICS LETTERS November 10, 2015
1671-7694/2015/111701(5) 111701-1 © 2015 Chinese Optics Letters
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