Piao Guanghao, Fan Limin, Zhang Yanmin, Jiang Wen, Guo Xiaoping, Liu Rui, Wang Qian, Jia Sihan, Liang Junqin, Li Yizhou
Department of Orthopedics, The Affiliated Hospital of Inner Mongolia Medical University, Hohhot, 010000, People's Republic of China.
Department of Orthopedics, Baogang Hospital of Inner Mongolia, Baotou, 014010, People's Republic of China.
Int J Nanomedicine. 2025 Jun 17;20:7743-7762. doi: 10.2147/IJN.S517633. eCollection 2025.
This study introduces a novel imaging approach for early detection of degenerative paraspinal muscle disorders, which are a key contributor to lower back pain and lumbar-related diseases. The core concept involves the use of a lanthanide-doped nanoprobe with a core@shell structure (NaYbF₄:x%Er@NaYF₄:x%Yb@NaYF₄), designed to function as a second near-infrared (NIR-II) fluorescent probe. This probe demonstrates significant advantages such as deep tissue penetration, high spatial and temporal resolution, and exceptional stability, enabling in vivo monitoring of muscle degeneration.
To achieve precise imaging of degenerative paraspinal muscles, a core@shell structure lanthanide nanoprobe of NaYbF4:x%Er@NaYF4:x%Yb @NaYF4 was designed through adjusting the lanthanide concentration parameters and outer shell structure thickness in the probe structure so that these adjustments improved its fluorescence efficiency and long fluorescence life. Based on the results of mRNA sequencing, our findings support Sidt2 as a reliable and potentially specific marker for paraspinal muscle degeneration. The fluorescent probe was functionalized with an antibody specifically targeting the upregulated lysosomal membrane protein Sidt2.
Notably, in a mice model of degenerative paraspinal muscles, the Sidt2-targeted nanoprobe selectively accumulated in the degenerative muscle tissues, displaying intense fluorescence signals. Fluorescence intensity measurements from the region of interest (ROI) in the degenerated paraspinal muscle showed NIR-II intensities of up to 200 a.u. with consistent fluorescence for 8 hours post-injection. Biological assays demonstrated a strong correlation between fluorescence intensity and the extent of muscle degeneration.
This study presents a platform for ultra-early detection of degenerative paraspinal muscles using NIR-II imaging, providing a theoretical basis for early intervention based on the multifunctionality of nanoprobes. This is the first application of NIR-II fluorescence imaging to assess muscle tissue lesions, and the results strongly support advancing to the next phase, which involves using multifunctional probe technology to intervene in paraspinal muscle degeneration.
本研究引入了一种用于早期检测椎旁肌退行性疾病的新型成像方法,这些疾病是下背痛和腰椎相关疾病的关键成因。其核心概念是使用具有核壳结构(NaYbF₄:x%Er@NaYF₄:x%Yb@NaYF₄)的镧系掺杂纳米探针,设计用作第二近红外(NIR-II)荧光探针。该探针具有诸如深层组织穿透、高空间和时间分辨率以及出色稳定性等显著优势,能够在体内监测肌肉退化。
为实现对退行性椎旁肌的精确成像,通过调整探针结构中的镧系元素浓度参数和外壳结构厚度,设计了一种NaYbF4:x%Er@NaYF4:x%Yb @NaYF4的核壳结构镧系纳米探针,以使这些调整提高其荧光效率和长荧光寿命。基于mRNA测序结果,我们的研究结果支持Sidt2作为椎旁肌退化的可靠且潜在特异性标志物。荧光探针用特异性靶向上调的溶酶体膜蛋白Sidt2的抗体进行功能化修饰。
值得注意的是,在退行性椎旁肌的小鼠模型中,靶向Sidt2的纳米探针选择性地积聚在退化的肌肉组织中,显示出强烈的荧光信号。来自退化椎旁肌感兴趣区域(ROI)的荧光强度测量显示,NIR-II强度高达200任意单位,注射后8小时荧光持续一致。生物学分析表明荧光强度与肌肉退化程度之间存在强相关性。
本研究提出了一个使用NIR-II成像超早期检测退行性椎旁肌的平台,为基于纳米探针多功能性的早期干预提供了理论基础。这是NIR-II荧光成像首次应用于评估肌肉组织病变,结果有力地支持推进到下一阶段,即使用多功能探针技术干预椎旁肌退化。