Histidine decarboxylase (HDC)-expressing granulocytic myeloid cells induce and recruit Foxp3+ regulatory T cells in murine colon cancer. (4th March 2017)
- Record Type:
- Journal Article
- Title:
- Histidine decarboxylase (HDC)-expressing granulocytic myeloid cells induce and recruit Foxp3+ regulatory T cells in murine colon cancer. (4th March 2017)
- Main Title:
- Histidine decarboxylase (HDC)-expressing granulocytic myeloid cells induce and recruit Foxp3+ regulatory T cells in murine colon cancer
- Authors:
- Chen, Xiaowei
Takemoto, Yoshihiro
Deng, Huan
Middelhoff, Moritz
Friedman, Richard A.
Chu, Timothy H.
Churchill, Michael J.
Ma, Yan
Nagar, Karan K.
Tailor, Yagnesh H.
Mukherjee, Siddhartha
Wang, Timothy C. - Abstract:
- ABSTRACT: The colorectal tumor microenvironment contains a diverse population of myeloid cells that are recruited and converted to immunosuppressive cells, thus facilitating tumor escape from immunoediting. We have identified a genetically and functionally distinct subset of dynamic bone marrow myeloid cells that are characterized by histidine decarboxylase (HDC) expression. Lineage tracing in Hdc-CreERT2;R26-LSL-tdTomato mice revealed that in homeostasis, there is a strong bias by HDC + myeloid cells toward the CD11b + Ly6G hi granulocytic lineage, which was accelerated during azoxymethane/dextran sodium sulfate (AOM/DSS)-induced colonic carcinogenesis. More importantly, HDC + myeloid cells strongly promoted colonic tumorigenesis, and colon tumor progression was profoundly suppressed by diphtheria toxin A (DTA)-mediated depletion of HDC + granulocytic myeloid cells. In addition, tumor infiltration by Foxp3 + regulatory T cells (Tregs) was markedly impaired following HDC + myeloid cell depletion. We identified an HDC + myeloid-derived Cxcl13/Cxcr5 axis that mediated Foxp3 expression and Treg proliferation. Ablation of HDC + myeloid cells or disruption of the Cxcl13/Cxcr5 axis by gene knockdown impaired the production and recruitment of Tregs. Cxcl13 induction of Foxp3 expression in Tregs during tumorigenesis was associated with Stat3 phosphorylation. Overall, HDC + granulocytic myeloid cells affect CD8 + T cells directly and indirectly through the modulation of Tregs andABSTRACT: The colorectal tumor microenvironment contains a diverse population of myeloid cells that are recruited and converted to immunosuppressive cells, thus facilitating tumor escape from immunoediting. We have identified a genetically and functionally distinct subset of dynamic bone marrow myeloid cells that are characterized by histidine decarboxylase (HDC) expression. Lineage tracing in Hdc-CreERT2;R26-LSL-tdTomato mice revealed that in homeostasis, there is a strong bias by HDC + myeloid cells toward the CD11b + Ly6G hi granulocytic lineage, which was accelerated during azoxymethane/dextran sodium sulfate (AOM/DSS)-induced colonic carcinogenesis. More importantly, HDC + myeloid cells strongly promoted colonic tumorigenesis, and colon tumor progression was profoundly suppressed by diphtheria toxin A (DTA)-mediated depletion of HDC + granulocytic myeloid cells. In addition, tumor infiltration by Foxp3 + regulatory T cells (Tregs) was markedly impaired following HDC + myeloid cell depletion. We identified an HDC + myeloid-derived Cxcl13/Cxcr5 axis that mediated Foxp3 expression and Treg proliferation. Ablation of HDC + myeloid cells or disruption of the Cxcl13/Cxcr5 axis by gene knockdown impaired the production and recruitment of Tregs. Cxcl13 induction of Foxp3 expression in Tregs during tumorigenesis was associated with Stat3 phosphorylation. Overall, HDC + granulocytic myeloid cells affect CD8 + T cells directly and indirectly through the modulation of Tregs and thus appear to play key roles in suppressing tumoricidal immunity. … (more)
- Is Part Of:
- Oncoimmunology. Volume 6:Number 3(2017)
- Journal:
- Oncoimmunology
- Issue:
- Volume 6:Number 3(2017)
- Issue Display:
- Volume 6, Issue 3 (2017)
- Year:
- 2017
- Volume:
- 6
- Issue:
- 3
- Issue Sort Value:
- 2017-0006-0003-0000
- Page Start:
- Page End:
- Publication Date:
- 2017-03-04
- Subjects:
- Colitis-associated colorectal cancer -- Cxcl13/Cxcr5 axis -- HDC+ myeloid cells -- immunosuppression -- regulatory T cells
Tumors -- Immunological aspects -- Periodicals
Neoplasms -- therapy -- Periodicals
Immunotherapy -- Periodicals
616.994 - Journal URLs:
- http://www.landesbioscience.com/journals/oncoimmunology/ ↗
http://www.tandfonline.com/toc/koni20/current ↗
http://www.tandf.co.uk/journals/ ↗ - DOI:
- 10.1080/2162402X.2017.1290034 ↗
- Languages:
- English
- ISSNs:
- 2162-402X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 5277.xml