Shelter in place: live CLL cells inside the bone marrow fibroblasts and its implication in residual disease persistence

作者：Pin Lu, Carrie A Franzen, Aldana Vistarop, Andrey Efimov, Sk Abrar Shahriyar, Shengchun Wang, Shilpa Rao, Marcus Messmer, Shazia Nakhoda, Edna Cukierman, Shuo Ma, Janusz Franco‐Barraza, Juehua Gao, Y. Lynn Wang · 发表于：Blood Neoplasia · 年份：2025 · DOI：10.1016/j.bneo.2025.100142 · 被引用次数：1 · 研究领域：Chronic Lymphocytic Leukemia Research、Chronic Myeloid Leukemia Treatments、Acute Lymphoblastic Leukemia research

Bruton tyrosine kinase inhibitors (BTKis) have been successful in treating B-cell malignancies including chronic lymphocytic leukemia (CLL). However, a deep response to BTK inhibition is uncommon. It is unknown what mechanism results in minimal residual disease (MRD) persistence. Cell-in-cell (CIC) describes the microscopic observations of embodiment of an intact cell by another whole cell. CIC has been sporadically described by pathologists in human fixed tissues for over a century. However, its biological, pathological, and clinical significance remains obscure. In this study, we investigated human primary CLL samples using a clinically faithful ex vivo model system that accurately recapitulates the lymphoma tumor microenvironment. We observed that CLL cells were actively internalized by Bone marrow fibroblasts (BMF) and remained alive and mobile for days. We hypothesized that live CIC may represent a new mechanism for tumor cells to evade therapies and survive as residual disease. Indeed, CIC events were identified directly in the bone marrow of patients being treated with BTKis. Using confocal microscopy, we demonstrated that the ex vivo exposure to BTKi drove CLL cells into BMF. We further showed that CIC inside the BMF were indeed protected from drug-induced apoptosis compared to cells that stayed outside. Mechanistically, we identified that CXCR4 receptor was required for CIC because CXCR4 antagonists and CRISPR-mediated genetic depletion completely abrogated CIC. Alto...