Immune Netw.  2018 Dec;18(6):e44. 10.4110/in.2018.18.e44.

Skewed Dendritic Cell Differentiation of MyD88-Deficient Donor Bone Marrow Cells, Instead of Massive Expansion as Myeloid-Derived Suppressor Cells, Aggravates GVHD

Affiliations
  • 1Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul 03080, Korea. eycii@snu.ac.kr
  • 2Institute of Human Environment Interface Biology, Seoul National University College of Medicine, Seoul 03080, Korea.
  • 3Department of Food and Nutrition, Seoul National University College of Human Ecology, Seoul 08826, Korea. shindm@snu.ac.kr
  • 4Department of Internal Medicine, Seoul St. Mary's Hospital, The Catholic University of Korea, Seoul 06951, Korea.

Abstract

Graft-versus-host disease (GVHD), a life-threatening complication after bone marrow transplantation (BMT), is induced by activation of alloreactive donor T cells. Our previous study demonstrated that transplantation of myeloid differentiation factor 88 (MyD88)-deficient knockout (KO) bone marrow (BM) resulted in aggravation of GVHD. Here, to understand the cellular mechanism, we performed longitudinal in vivo imaging and flow cytometric analyses followed by transcriptome and functional examination of donor MyD88-KO BM progenies in GVHD hosts, using a major histocompatibility complex-matched but minor histocompatibility antigen-mismatched C57BL/6→BALB.B model. In GVHD hosts with MyD88-KO BMT, donor BM-derived CD11b+Gr-1+ cells were found to undergo cell death, a fate significantly different from the explosive expansion shown by the wild type (WT) counterparts, and also from the moderate expansion of the WT or MyD88-KO BM-derived cells in non-GVHD hosts. It was also revealed that MyD88-KO CD11b+Gr-1+ cells preferred differentiation into CD11c+ dendritic cells (DCs) to expansion as myeloid-derived suppressor cells in GVHD hosts or in high inflammatory in vitro conditions. These CD11c+ DCs comprised the majority of MyD88-KO CD11b+Gr-1+ apoptotic cells in GVHD hosts. Their ability to cross-present alloantigens of host origin contributed to the enhancement of T cell alloreactivity, causing GVHD aggravation and eventually death through the killing function of activated T cells. These results provide insights into the roles of MyD88 in myelopoiesis of donor BM and the protective effects in GVHD hosts, helpful information for development of a strategy to control GVHD.

Keyword

Bone marrow transplantation; Dendritic cells; Graft-versus-host disease; Myeloid differentiation factor 88; Myeloid-derived suppressor cells

MeSH Terms

Bone Marrow Cells*
Bone Marrow Transplantation
Bone Marrow*
Cell Death
Dendritic Cells*
Graft vs Host Disease
Histocompatibility
Homicide
Humans
In Vitro Techniques
Isoantigens
Myeloid Differentiation Factor 88
Myelopoiesis
T-Lymphocytes
Tissue Donors*
Transcriptome
Isoantigens
Myeloid Differentiation Factor 88
Full Text Links
  • IN
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr