Understanding heterogeneity of human bone marrow plasma cell maturation and survival pathways by single-cell analyses

Bibliographic Details
Title: Understanding heterogeneity of human bone marrow plasma cell maturation and survival pathways by single-cell analyses
Authors: Meixue Duan, Doan C. Nguyen, Chester J. Joyner, Celia L. Saney, Christopher M. Tipton, Joel Andrews, Sagar Lonial, Caroline Kim, Ian Hentenaar, Astrid Kosters, Eliver Ghosn, Annette Jackson, Stuart Knechtle, Stalinraja Maruthamuthu, Sindhu Chandran, Tom Martin, Raja Rajalingam, Flavio Vincenti, Cynthia Breeden, Ignacio Sanz, Greg Gibson, F. Eun-Hyung Lee
Source: Cell Reports, Vol 42, Iss 7, Pp 112682- (2023)
Publisher Information: Elsevier, 2023.
Publication Year: 2023
Collection: LCC:Biology (General)
Subject Terms: CP: Immunology, Biology (General), QH301-705.5
More Details: Summary: Human bone marrow (BM) plasma cells are heterogeneous, ranging from newly arrived antibody-secreting cells (ASCs) to long-lived plasma cells (LLPCs). We provide single-cell transcriptional resolution of 17,347 BM ASCs from five healthy adults. Fifteen clusters are identified ranging from newly minted ASCs (cluster 1) expressing MKI67 and high major histocompatibility complex (MHC) class II that progress to late clusters 5–8 through intermediate clusters 2–4. Additional ASC clusters include the following: immunoglobulin (Ig) M predominant (likely of extra-follicular origin), interferon responsive, and high mitochondrial activity. Late ASCs are distinguished by G2M checkpoints, mammalian target of rapamycin (mTOR) signaling, distinct metabolic pathways, CD38 expression, utilization of tumor necrosis factor (TNF)-receptor superfamily members, and two distinct maturation pathways involving TNF signaling through nuclear factor κB (NF-κB). This study provides a single-cell atlas and molecular roadmap of LLPC maturation trajectories essential in the BM microniche. Altogether, understanding BM ASC heterogeneity in health and disease enables development of new strategies to enhance protective ASCs and to deplete pathogenic ones.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2211-1247
Relation: http://www.sciencedirect.com/science/article/pii/S2211124723006939; https://doaj.org/toc/2211-1247
DOI: 10.1016/j.celrep.2023.112682
Access URL: https://doaj.org/article/e2cfa9f8c92144a5ae6fadda3ba129f7
Accession Number: edsdoj.2cfa9f8c92144a5ae6fadda3ba129f7
Database: Directory of Open Access Journals
More Details
ISSN:22111247
DOI:10.1016/j.celrep.2023.112682
Published in:Cell Reports
Language:English