Note (General)application/pdf
Hematopoiesis was considered a hierarchical stepwise process but was revised to a continuous process following single-cell RNA sequencing. However, the uncertainty or fluctuation of single-cell transcriptome dynamics during differentiation was not considered, and the dendritic cell (DC) pathway in the lymphoid context remains unclear. Here, we identify human B-plasmacytoid DC (pDC) bifurcation as large fluctuating transcriptome dynamics in the putative B/NK progenitor region by dry and wet methods. By converting splicing kinetics intodiffusiondynamics in a deepgenerativemodel,our original computationalmethodology reveals strongfluctuation at B/pDC bifurcation in IL-7Ra+ regions, and LFA-1 fluctuates positively in the pDCdirection at the bifurcation. These expectancies are validated by the presence of B/pDCprogenitors in the IL-7Ra+ fraction and preferential expression of LFA-1 in pDC-biased progenitors with a niche-like culture system.Weprovide a model of fluctuation-based differentiation, which reconciles continuous and discrete models and is applicable to other developmental systems.
本文/Department of Hematology and Oncology, Mie University Graduate School of Medicine, Tsu 514-8507, Japan
22p
Collection (particular)国立国会図書館デジタルコレクション > デジタル化資料 > 博士論文
Date Accepted (W3CDTF)2023-10-11T15:41:06+09:00
Data Provider (Database)国立国会図書館 : 国立国会図書館デジタルコレクション