Tanshinone IIA and Cryptotanshinone Counteract Inflammation by Regulating Gene and miRNA Expression in Human SGBS Adipocytes

Author:

Carpi Sara123ORCID,Quarta Stefano4ORCID,Doccini Stefano5ORCID,Saviano Anella6,Marigliano Noemi6,Polini Beatrice37ORCID,Massaro Marika8,Carluccio Maria Annunziata8ORCID,Calabriso Nadia8ORCID,Wabitsch Martin9ORCID,Santorelli Filippo Maria5,Cecchini Marco2ORCID,Maione Francesco6ORCID,Nieri Paola3ORCID,Scoditti Egeria8ORCID

Affiliation:

1. Science of Health Department, Magna Græcia University, 88100 Catanzaro, Italy

2. NEST, Istituto Nanoscienze-CNR and Scuola Normale Superiore, 56100 Pisa, Italy

3. Department of Pharmacy, University of Pisa, 56100 Pisa, Italy

4. Department of Biological and Environmental Sciences and Technologies (DISTEBA), University of Salento, 73100 Lecce, Italy

5. IRCCS Fondazione Stella Maris, Calambrone, 56128 Pisa, Italy

6. ImmunoPharmaLab, Department of Pharmacy, School of Medicine and Surgery, University of Naples Federico II, 80131 Naples, Italy

7. Department of Pathology, University of Pisa, 56100 Pisa, Italy

8. National Research Council (CNR), Institute of Clinical Physiology (IFC), 73100 Lecce, Italy

9. Division of Pediatric Endocrinology, Diabetes and Obesity, Department of Pediatrics and Adolescent Medicine, University of Ulm, 89075 Ulm, Germany

Abstract

Inflammation of the adipose tissue contributes to the onset and progression of several chronic obesity-related diseases. The two most important lipophilic diterpenoid compounds found in the root of Salvia milthorrhiza Bunge (also called Danshen), tanshinone IIA (TIIA) and cryptotanshinone (CRY), have many favorable pharmacological effects. However, their roles in obesity-associated adipocyte inflammation and related sub-networks have not been fully elucidated. In the present study, we investigated the gene, miRNAs and protein expression profile of prototypical obesity-associated dysfunction markers in inflamed human adipocytes treated with TIIA and CRY. The results showed that TIIA and CRY prevented tumor necrosis factor (TNF)-α induced inflammatory response in adipocytes, by counter-regulating the pattern of secreted cytokines/chemokines associated with adipocyte inflammation (CCL2/MCP-1, CXCL10/IP-10, CCL5/RANTES, CXCL1/GRO-α, IL-6, IL-8, MIF and PAI-1/Serpin E1) via the modulation of gene expression (as demonstrated for CCL2/MCP-1, CXCL10/IP-10, CCL5/RANTES, CXCL1/GRO-α, and IL-8), as well as related miRNA expression (miR-126-3p, miR-223-3p, miR-124-3p, miR-155-5p, and miR-132-3p), and by attenuating monocyte recruitment. This is the first demonstration of a beneficial effect by TIIA and CRY on adipocyte dysfunction associated with obesity development and complications, offering a new outlook for the prevention and/or treatment of metabolic diseases.

Funder

MIUR

Publisher

MDPI AG

Subject

Molecular Biology,Biochemistry

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