Your browser doesn't support javascript.
loading
Development of a Mature B Lymphocyte Probe through Gating-Oriented Live-Cell Distinction (GOLD) and Selective Imaging of Topical Spleen.
Cho, Heewon; Kwon, Haw-Young; Kim, Youngsook; Kim, Kyungwon; Lee, Eun Jig; Kang, Nam-Young; Chang, Young-Tae.
  • Cho H; Department of Chemistry, Pohang University of Science and Technology (POSTECH), Pohang, Gyeongsangbuk-do 37673, Republic of Korea.
  • Kwon HY; Department of Chemistry, Pohang University of Science and Technology (POSTECH), Pohang, Gyeongsangbuk-do 37673, Republic of Korea.
  • Kim Y; Center for Self-Assembly and Complexity, Institute for Basic Science (IBS), Pohang, Gyeongsangbuk-do 37673, Republic of Korea.
  • Kim K; Endocrinology, Institute of Endocrine Research, Department of Internal Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
  • Lee EJ; Endocrinology, Institute of Endocrine Research, Department of Internal Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
  • Kang NY; Endocrinology, Institute of Endocrine Research, Department of Internal Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
  • Chang YT; Department of Convergence IT Engineering, Pohang University of Science and Technology (POSTECH), Pohang, Gyeongsangbuk-do 37673, Republic of Korea.
JACS Au ; 4(4): 1450-1457, 2024 Apr 22.
Article en En | MEDLINE | ID: mdl-38665660
ABSTRACT
B lymphocytes play a pivotal role in the adaptive immune system by facilitating antibody production. Young B cell progenitors originate in the bone marrow and migrate to the spleen for antigen-dependent maturation, leading to the development of diverse B cell subtypes. Thus, tracking B cell trajectories through cell type distinction is essential for an appropriate checkpoint assessment. Despite its significance, monitoring specific B cell subclasses in live states has been hindered by a lack of suitable molecular tools. In this study, we introduce CDoB as the first mature B cell-selective probe, enabling real-time discrimination of three classified stages in B-cell development progenitor, transitional, and mature B cells, through a single analysis using CyTOF. The selective mechanism of CDoB, elucidated as gating-oriented live-cell distinction (GOLD), targets SLC25A16, identified through systematic screening of SLC-CRISPRa and CRISPRi libraries. CDoB selectively brightens mature B cells in the mitochondrial area using SLC25A16 as the main gate, and the staining intensity correlates positively with the expression level of SLC25A16 along the B cell maturation continuum. In spleen tissues, CDoB demonstrates selective marking in mature B cell areas in live tissue status, representing the first performance achieved by a small-molecule fluorescent probe.