Abstract
Dendritic cells (DCs) play key roles in the interface between innate and adaptive immunity. They are capable of detecting a wide range of pathogens and other stimuli; they internalize, process, and present antigens; and they modulate the activity of other immune cells. Recent advances have demonstrated that distinct subsets of DCs play unique roles at steady state and under inflammatory conditions. We found that the transcription factors Bcl11a and Zeb2 are each essential for development of plasmacytoid DCs but dispensable for development of classical DCs in vivo. Zeb2-deficient bone marrow cells are also deficient in replenishment of monocytes, which along with their macrophage progeny represent a hematopoietic lineage closely related to that of DCs. Finally, we developed a lineage-tracing mouse strain using Cre recombinase under the control of the transcription factor-encoding locus Mafb; with that model, we determined that Langerhans cells in the skin are unique in displaying certain characteristics of both macrophages and DCs.
Committee Chair
Kenneth M. Murphy
Committee Members
Deepta Bhattacharya, Marco Colonna, Takeshi Egawa, Thaddeus S. Stappenbeck,
Degree
Doctor of Philosophy (PhD)
Author's Department
Biology & Biomedical Sciences (Immunology)
Document Type
Dissertation
Date of Award
Spring 5-15-2018
Language
English (en)
DOI
https://doi.org/10.7936/K76M368H
Recommended Citation
Wu, Xiaodi, "Classical Dendritic Cell Development Excludes Alternative Myeloid Cell Fates Characterized by Distinct Transcription Factors" (2018). Arts & Sciences Theses and Dissertations. 1601.
The definitive version is available at https://doi.org/10.7936/K76M368H
Comments
Permanent URL: https://doi.org/10.7936/K76M368H