Langerhans cells (LC) reside in the epidermis of the skin--a barrier site that provides LC access to cutaneous pathogens and neoplasia as well as benign commensal microorganisms. Work from our group and others indicates that LC suppress immune responses to cutaneous antigen in vivo and may prevent inappropriate responses to skin commensal microorganisms. A key regulated step in the life-cycle of LC is activation and migration from the epidermis to the lymph node where they present antigen to T cells. LC migration occurs in response to a variety of inflammatory stimuli. Though IL- 12 and TNF1 are thought to be key mediators of LC migration, introduction of pharmacological levels of these cytokines in vivo induces migration of only a relatively small number of LC suggesting that other mechanisms of LC activation/migration exist. We have previously shown that LC development requires autocrine TGF21. To examine the role of TGF21 in the steady state, we have recently developed transgenic mice that express tamoxifen inducible Cre selectively in LC. When bred to TGF21-flox mice, tamoxifen injection ablates TGF21 from adult LC and induces spontaneous activation and migration of virtually all LC. Based on this unexpected finding, we hypothesize that autocrine TGF21 signaling plays a key role in LC migration. We propose a model in which TGF21 secreted by LC is activated by integrin av26 on keratinocytes and then acts directly on LC to maintain their immature state. When keratonocytes encounter a danger signal, they decrease surface expression of av26 thereby reducing the amount of activated TGF21 available to LC. The resulting decreased levels of TGF21 signaling in LC promotes their activation and migration. This represents a novel mechanism of DC activation that would have a significant impact on skin and DC biology in general could provide a therapeutic target for the inhibition LC activation. The objective of this proposal is to test the validity of this hypothesis and explore its underlying mechanisms.

Public Health Relevance

Langerhans cells (LC) are the prototypic tissue-type DC that reside in the epidermis of the skin where they are exposed to cutaneous pathogens and neoplasia as well as benign commensal microorganisms. A key regulated step in the life-cycle of LC is activation and migration from the epidermis to the lymph node where they present antigen to T cells. Based on our novel discovery that the ablation of TGF21 in LC results in activation and migration, we hypothesize that TGF21 signaling plays a key role in regulating this process. The objective of this proposal is to test the validity of this hypothesis and explore its underlying mechanisms.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
5R01AR060744-03
Application #
8508067
Study Section
Arthritis, Connective Tissue and Skin Study Section (ACTS)
Program Officer
Cibotti, Ricardo
Project Start
2011-09-15
Project End
2016-07-31
Budget Start
2013-08-01
Budget End
2014-07-31
Support Year
3
Fiscal Year
2013
Total Cost
$322,763
Indirect Cost
$109,013
Name
University of Minnesota Twin Cities
Department
Dermatology
Type
Schools of Medicine
DUNS #
555917996
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Kashem, Sakeen W; Kaplan, Daniel H (2018) Isolation of Murine Skin Resident and Migratory Dendritic Cells via Enzymatic Digestion. Curr Protoc Immunol 121:e45
Kashem, Sakeen W; Haniffa, Muzlifah; Kaplan, Daniel H (2017) Antigen-Presenting Cells in the Skin. Annu Rev Immunol 35:469-499
Kaplan, Daniel H (2017) Ontogeny and function of murine epidermal Langerhans cells. Nat Immunol 18:1068-1075
Strandt, Helen; Pinheiro, Douglas Florindo; Kaplan, Daniel H et al. (2017) Neoantigen Expression in Steady-State Langerhans Cells Induces CTL Tolerance. J Immunol 199:1626-1634
Mohammed, Javed; Beura, Lalit K; Bobr, Aleh et al. (2016) Stromal cells control the epithelial residence of DCs and memory T cells by regulated activation of TGF-?. Nat Immunol 17:414-21
Kashem, Sakeen W; Kaplan, Daniel H (2016) Skin Immunity to Candida albicans. Trends Immunol 37:440-450
Huang, Huizhen; Kuzirian, Marissa S; Cai, Xiaoyun et al. (2016) Generation of a NK1R-CreER knockin mouse strain to study cells involved in Neurokinin 1 Receptor signaling. Genesis 54:593-601
Scholz, Felix; Naik, Shruti; Sutterwala, Fayyaz S et al. (2015) Langerhans Cells Suppress CD49a+ NK Cell-Mediated Skin Inflammation. J Immunol 195:2335-42
Kashem, Sakeen W; Igyarto, Botond Z; Gerami-Nejad, Maryam et al. (2015) Candida albicans morphology and dendritic cell subsets determine T helper cell differentiation. Immunity 42:356-366
Kashem, Sakeen W; Riedl, Maureen S; Yao, Chen et al. (2015) Nociceptive Sensory Fibers Drive Interleukin-23 Production from CD301b+ Dermal Dendritic Cells and Drive Protective Cutaneous Immunity. Immunity 43:515-26

Showing the most recent 10 out of 18 publications