Human B-cell development at the single-cell level
Abstract
B cells play an integral part of our immune system. In adults they develop in the bone marrow in a regulated process in which the specificity of their B-cell antigen receptor (BCR), a membrane bound antibody, is established. This is generated by somatic recombination of immunoglobulin (Ig) gene segments that encode the antigen binding region of Ig heavy and light chains. Most studies of B-cell development have been carried out in mouse models, while those in humans have mainly been performed at the population level. This thesis aimed to delineate early B-cell development in human bone marrow and investigate how the BCR repertoire is shaped, at the single-cell level. To this end, we analysed human bone marrow early B-lineage cells using flow cytometry and 5’ single-cell RNA- and VDJ sequencing.
In Paper I, we investigated the influence of BCR and T-cell antigen receptor genes on unsupervised clustering and downstream analyses in 5’ single-cell RNA sequencing data from B and T cells. In Paper II, we aimed to delineate the stages of B-cell development in the adult human bone marrow at the single-cell level and investigate how the BCR repertoire is shaped throughout development. In Paper III, we analysed the expression of Ig light chain transcripts during B-cell development, to infer recombination status of the kappa and lambda light chain loci.
In conclusion, we have developed a protocol to analyse 5’ single-cell RNA sequencing data which generates biologically relevant clusters of B and T cells. By using flow cytometry and the protocol developed in Paper I to analyse 5’ single-cell RNA and VDJ sequencing data, we can put forward a novel model of human B-cell development, which includes shaping of the BCR repertoire from the earliest pro-B cells to mature naïve B cells. For instance, we show a step-wise selection of the BCR repertoire, mainly exerted on the H-CDR3 region. Moreover, our data indicate that recombination of Ig lambda light chain is independent of that of kappa, a model that challenges the current dogma.
Parts of work
1) Timothy Sundell, Kristoffer Grimstad, Alessandro Camponeschi, Andreas Tilevik, Inger Gjertsson, Inga-Lill Mårtensson. Single-cell RNA sequencing analyses: interference by the genes that encode the B-cell and T-cell receptors, Briefings in Functional Genomics, Volume 22, Issue 3, May 2023, Pages 263–273, https://doi.org/10.1093/bfgp/elac044 2) Timothy Sundell, Alessandro Camponeschi, Alaitz Aranburu, Gustav Arvidsson, Jessica Nordlund, Ann-Christine Syvänen, Gunnel Nordmark, Inger Gjertsson, Inga-Lill Mårtensson. Shaping the human immune repertoire. Manuscript (2024) 3) Timothy Sundell*, Alessandro Camponeschi*, Alaitz Aranburu, Gustav Arvidsson, Jessica Nordlund, Ann-Christine Syvänen, Gunnel Nordmark, Inger Gjertsson, Inga-Lill Mårtensson. Ig light chain recombination and expression during human B-cell development. Manuscript (2024)
* Equal contribution.
Degree
Doctor of Philosophy (Medicine)
University
University of Gothenburg. Sahlgrenska Academy
Institution
Institute of Medicine. Department of Rheumatology and Inflammation Research
Disputation
Torsdagen den 12 december 2024, kl. 9.00, Föreläsningssal vån. 3, Guldhedsgatan 10A, Göteborg
Date of defence
2024-12-12
timothy.sundell@gu.se
Date
2024-11-21Author
Sundell, Timothy
Keywords
B-cell development
BCR
Tolerance
single-cell RNA-sequencing
Publication type
Doctoral thesis
ISBN
978-91-8069-929-7 (PRINT)
978-91-8069-930-3 (PDF)
Language
eng