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A Synthetic Cell-Penetrating Heparin-Binding Peptide Derived from BMP4 with Anti-Inflammatory and Chondrogenic Functions for the Treatment of Arthritis

We report dual therapeutic effects of a synthetic heparin-binding peptide (HBP) corresponding to residues 15–24 of the heparin binding site in BMP4 in a collagen-induced rheumatic arthritis model (CIA) for the first time. The cell penetrating capacity of HBP led to improved cartilage recovery and an...

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Autores principales: Choi, Da Hyeon, Lee, Dongwoo, Jo, Beom Soo, Park, Kwang-Sook, Lee, Kyeong Eun, Choi, Ju Kwang, Park, Yoon Jeong, Lee, Jue-Yeon, Park, Yoon Shin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352680/
https://www.ncbi.nlm.nih.gov/pubmed/32549254
http://dx.doi.org/10.3390/ijms21124251
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author Choi, Da Hyeon
Lee, Dongwoo
Jo, Beom Soo
Park, Kwang-Sook
Lee, Kyeong Eun
Choi, Ju Kwang
Park, Yoon Jeong
Lee, Jue-Yeon
Park, Yoon Shin
author_facet Choi, Da Hyeon
Lee, Dongwoo
Jo, Beom Soo
Park, Kwang-Sook
Lee, Kyeong Eun
Choi, Ju Kwang
Park, Yoon Jeong
Lee, Jue-Yeon
Park, Yoon Shin
author_sort Choi, Da Hyeon
collection PubMed
description We report dual therapeutic effects of a synthetic heparin-binding peptide (HBP) corresponding to residues 15–24 of the heparin binding site in BMP4 in a collagen-induced rheumatic arthritis model (CIA) for the first time. The cell penetrating capacity of HBP led to improved cartilage recovery and anti-inflammatory effects via down-regulation of the iNOS-IFNγ-IL6 signaling pathway in inflamed RAW264.7 cells. Both arthritis and paw swelling scores were significantly improved following HBP injection into CIA model mice. Anti-rheumatic effects were accelerated upon combined treatment with Enbrel(®) and HBP. Serum IFNγ and IL6 concentrations were markedly reduced following intraperitoneal HBP injection in CIA mice. The anti-rheumatic effects of HBP in mice were similar to those of Enbrel(®). Furthermore, the combination of Enbrel(®) and HBP induced similar anti-rheumatic and anti-inflammatory effects as Enbrel(®). We further investigated the effect of HBP on damaged chondrocytes in CIA mice. Regenerative capacity of HBP was confirmed based on increased expression of chondrocyte biomarker genes, including aggrecan, collagen type II and TNFα, in adult human knee chondrocytes. These findings collectively support the utility of our cell-permeable bifunctional HBP with anti-inflammatory and chondrogenic properties as a potential source of therapeutic agents for degenerative inflammatory diseases.
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spelling pubmed-73526802020-07-21 A Synthetic Cell-Penetrating Heparin-Binding Peptide Derived from BMP4 with Anti-Inflammatory and Chondrogenic Functions for the Treatment of Arthritis Choi, Da Hyeon Lee, Dongwoo Jo, Beom Soo Park, Kwang-Sook Lee, Kyeong Eun Choi, Ju Kwang Park, Yoon Jeong Lee, Jue-Yeon Park, Yoon Shin Int J Mol Sci Article We report dual therapeutic effects of a synthetic heparin-binding peptide (HBP) corresponding to residues 15–24 of the heparin binding site in BMP4 in a collagen-induced rheumatic arthritis model (CIA) for the first time. The cell penetrating capacity of HBP led to improved cartilage recovery and anti-inflammatory effects via down-regulation of the iNOS-IFNγ-IL6 signaling pathway in inflamed RAW264.7 cells. Both arthritis and paw swelling scores were significantly improved following HBP injection into CIA model mice. Anti-rheumatic effects were accelerated upon combined treatment with Enbrel(®) and HBP. Serum IFNγ and IL6 concentrations were markedly reduced following intraperitoneal HBP injection in CIA mice. The anti-rheumatic effects of HBP in mice were similar to those of Enbrel(®). Furthermore, the combination of Enbrel(®) and HBP induced similar anti-rheumatic and anti-inflammatory effects as Enbrel(®). We further investigated the effect of HBP on damaged chondrocytes in CIA mice. Regenerative capacity of HBP was confirmed based on increased expression of chondrocyte biomarker genes, including aggrecan, collagen type II and TNFα, in adult human knee chondrocytes. These findings collectively support the utility of our cell-permeable bifunctional HBP with anti-inflammatory and chondrogenic properties as a potential source of therapeutic agents for degenerative inflammatory diseases. MDPI 2020-06-15 /pmc/articles/PMC7352680/ /pubmed/32549254 http://dx.doi.org/10.3390/ijms21124251 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Choi, Da Hyeon
Lee, Dongwoo
Jo, Beom Soo
Park, Kwang-Sook
Lee, Kyeong Eun
Choi, Ju Kwang
Park, Yoon Jeong
Lee, Jue-Yeon
Park, Yoon Shin
A Synthetic Cell-Penetrating Heparin-Binding Peptide Derived from BMP4 with Anti-Inflammatory and Chondrogenic Functions for the Treatment of Arthritis
title A Synthetic Cell-Penetrating Heparin-Binding Peptide Derived from BMP4 with Anti-Inflammatory and Chondrogenic Functions for the Treatment of Arthritis
title_full A Synthetic Cell-Penetrating Heparin-Binding Peptide Derived from BMP4 with Anti-Inflammatory and Chondrogenic Functions for the Treatment of Arthritis
title_fullStr A Synthetic Cell-Penetrating Heparin-Binding Peptide Derived from BMP4 with Anti-Inflammatory and Chondrogenic Functions for the Treatment of Arthritis
title_full_unstemmed A Synthetic Cell-Penetrating Heparin-Binding Peptide Derived from BMP4 with Anti-Inflammatory and Chondrogenic Functions for the Treatment of Arthritis
title_short A Synthetic Cell-Penetrating Heparin-Binding Peptide Derived from BMP4 with Anti-Inflammatory and Chondrogenic Functions for the Treatment of Arthritis
title_sort synthetic cell-penetrating heparin-binding peptide derived from bmp4 with anti-inflammatory and chondrogenic functions for the treatment of arthritis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352680/
https://www.ncbi.nlm.nih.gov/pubmed/32549254
http://dx.doi.org/10.3390/ijms21124251
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