用张量补全方法恢复荧光显微镜下的稀疏3D细胞图像，提升信噪比与结构保真度。

Fluorescence microscopy (FM) imaging is a fundamental technique for observing live cell division, one of the most essential processes in the cycle of life and death. Observing 3D live cells requires scanning through the cell volume while minimizing lethal phototoxicity. That limits acquisition time and results in sparsely sampled volumes with anisotropic resolution and high noise. Existing image restoration methods, primarily based on inverse problem modeling, assume known and stable degradation processes and struggle under such conditions, especially in the absence of high-quality reference volumes. In this paper, from a new perspective, we propose a novel tensor completion framework tailored to the nature of FM imaging, which inherently involves nonlinear signal degradation and incomplete observations. Specifically, FM imaging with equidistant Z-axis sampling is essentially a tensor completion task under a uniformly random sampling condition. On one hand, we derive the theoretical lower bound for exact cell tensor completion, validating the feasibility of accurately recovering 3D cell tensor. On the other hand, we reformulate the tensor completion problem as a mathematically equivalent score-based generative model. By incorporating structural consistency priors, the generative trajectory is effectively guided toward denoised and geometrically coherent reconstructions. Our method demonstrates state-of-the-art performance on SR-CACO-2 and three real \textit{in vivo} cellular datasets, showing substantial improvements in both signal-to-noise ratio and structural fidelity.