Discovery of CYP11A1 initiated metabolism of pro-vitamin D to 7? steroids (subject to UVB photoconversion to corresponding secosteroids) and sequential hydroxylation of vitamin D producing 20(OH)D3 and other hydroxyderivatives, defined new metabolic pathways of which the main intermediate, 20(OH)D3, is biologically active, while being nontoxic and noncalcemic in rats and mice at doses as high as 60 ?kg. These pathways can operate ex vivo in placenta, adrenal gland and epidermal keratinocytes. We also detected 20(OH)D3 in human serum. 20(OH)D3 is at least as potent as 1,25(OH)2D3 in anti-proliferative, pro-differentiation and anti-inflammatory assays and attenuates development of bleomycin induced fibrosis in mice. However, a major barrier for using 20(OH)D3 in preclinical models of scleroderma is a lack of understanding of the mechanism of its action on dermal fibroblasts. The goal of this R21 is to test hypothesis is that 20(OH)D3 acting directly on vitamin D receptor (VDR)- or/and on retinoic acid orphan receptor (ROR)- dependent mechanisms inhibit profibrotic fibroblast activities. To study this hypothesis one mechanistically oriented specific aim is designed with four subaims: 1. To test the mechanism of antifibrotic action of 20(OH)D3 in dermal fibroblasts.
Sub aim 1 : We will investigate which signaling pathways utilized by TGF-?1 in dermal fibroblasts are inhibited by 20(OH)D3. We will determine whether this secosteroid inhibits other profibrotic effects of TGF-?1 and determine its relative potency on each pathway;
Sub aim 2 : We will investigate the involvement of VDR-dependent pathways by testing the effects of 20(OH)D3 on fibroblasts derived from VDR-/- mice. Confirmations for humans will be carried out using dermal fibroblasts with receptors silenced by RNAi technology. These will be complemented by quantitative testing of ligand-induced VDR translocation to the nucleus and activation of VDRE transcriptional activity using VDR-GFP and VDRE-LUC constructs, respectively;
Sub aim 3 : The hypothesis that 20(OH)D3 acting on ROR? and ROR? will regulate fibroblast activities will be tested. We will define interactions of 20(OH)D3 with ROR? and ROR? using biochemical and cell-based assays. Involvement of those receptors in the regulation of a phenotype will be evaluated using fibroblasts from ROR?- and ROR?-/- mice with further confirmation in human dermal fibroblasts with receptors silenced by RNAi. Divergence and overlaps between the actions on VDR, ROR? and ROR? will also be tested by whole genome RNAseq analysis supplemented by testing gene expression and bioinformatic analysis. This will define which phenotypic traits are regulated by VDR and which by ROR? or ROR?;
Sub aim 4 : We will test whether antifibrotic activity of 20(OH)D3 is regulated by hydroxylation at C1? and/or C25. Techniques of biochemistry, gene silencing technology and cell biology will be used and will further be supplemented by pharmacological approaches. Defining which phenotypic treats are regulated through VDR or ROR? and ROR? by 20(OH)D3, would allow to perform future testing on proper KO mice to define role of the receptor in in vivo scleroderma models.

Public Health Relevance

We will define mechanisms of action of 20-hydroxyvitamin D3, the main intermediate of newly discovered metabolic pathway of vitamin D3 metabolism started by the action of CYP11A1 and modified by CYP27B1 activity. These studies are necessary for projected in vivo preclinical studies prior the planned Phase I clinical trials on scleroderma. .

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21AR066505-01A1
Application #
8833514
Study Section
Arthritis, Connective Tissue and Skin Study Section (ACTS)
Program Officer
Tseng, Hung H
Project Start
2014-09-18
Project End
2016-08-31
Budget Start
2014-09-18
Budget End
2015-08-31
Support Year
1
Fiscal Year
2014
Total Cost
$198,000
Indirect Cost
$66,000
Name
University of Tennessee Health Science Center
Department
Pathology
Type
Schools of Medicine
DUNS #
941884009
City
Memphis
State
TN
Country
United States
Zip Code
38163
Manna, Pulak R; Stetson, Cloyce L; Slominski, Andrzej T et al. (2016) Role of the steroidogenic acute regulatory protein in health and disease. Endocrine 51:7-21
Slominski, Andrzej T; Kim, Tae-Kang; Hobrath, Judith V et al. (2016) Endogenously produced nonclassical vitamin D hydroxy-metabolites act as "biased" agonists on VDR and inverse agonists on RORα and RORγ. J Steroid Biochem Mol Biol :
Lin, Zongtao; Marepally, Srinivasa R; Kim, Tae-Kang et al. (2016) Design, Synthesis and Biological Activities of Novel Gemini 20S-Hydroxyvitamin D3 Analogs. Anticancer Res 36:877-86
Brożyna, Anna A; Jóżwicki, Wojciech; Skobowiat, Cezary et al. (2016) RORα and RORγ expression inversely correlates with human melanoma progression. Oncotarget :
Slominski, Andrzej T; Zmijewski, Michal A; Jetten, Anton M (2016) RORα is not a receptor for melatonin (response to DOI 10.1002/bies.201600018). Bioessays 38:1193-1194
Płonka, Przemysław M; Picardo, Mauro; Slominski, Andrzej T (2016) Does melanin matter in the dark? Exp Dermatol :
Skobowiat, Cezary; Slominski, Andrzej T (2016) Ultraviolet B stimulates proopiomelanocortin signalling in the arcuate nucleus of the hypothalamus in mice. Exp Dermatol 25:120-3
Skobowiat, Cezary; Postlethwaite, Arnold E; Slominski, Andrzej T (2016) Skin Exposure to Ultraviolet B Rapidly Activates Systemic Neuroendocrine and Immunosuppressive Responses. Photochem Photobiol :
Wierzbicka, Justyna M; Żmijewski, Michał A; Piotrowska, Anna et al. (2016) Bioactive forms of vitamin D selectively stimulate the skin analog of the hypothalamus-pituitary-adrenal axis in human epidermal keratinocytes. Mol Cell Endocrinol 437:312-322
Skobowiat, Cezary; Slominski, Andrzej T (2016) Sun-derived infrared A and ultraviolet B radiation: allies or enemies in melanomagenesis? Exp Dermatol 25:760-2

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