BMP-9 Improves the Osteogenic Differentiation Ability over BMP-2 through p53 Signaling In Vitro in Human Periosteum-Derived Cells
Bone morphogenetic proteins (BMPs) have tremendous therapeutic potential regarding the treatment of bone and musculoskeletal disorders due to their osteo-inductive ability. More than twenty BMPs have been identified in the human body with various functions, such as embryonic development, skeleton ge...
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2023-10-01
|
Series: | International Journal of Molecular Sciences |
Subjects: | |
Online Access: | https://www.mdpi.com/1422-0067/24/20/15252 |
_version_ | 1797573642055319552 |
---|---|
author | Jin-Ho Park Eun-Byeol Koh Young-Jin Seo Hye-Seong Oh June-Ho Byun |
author_facet | Jin-Ho Park Eun-Byeol Koh Young-Jin Seo Hye-Seong Oh June-Ho Byun |
author_sort | Jin-Ho Park |
collection | DOAJ |
description | Bone morphogenetic proteins (BMPs) have tremendous therapeutic potential regarding the treatment of bone and musculoskeletal disorders due to their osteo-inductive ability. More than twenty BMPs have been identified in the human body with various functions, such as embryonic development, skeleton genesis, hematopoiesis, and neurogenesis. BMPs can induce the differentiation of MSCs into the osteoblast lineage and promote the proliferation of osteoblasts and chondrocytes. BMP signaling is also involved in tissue remodeling and regeneration processes to maintain homeostasis in adults. In particular, growth factors, such as BMP-2 and BMP-7, have already been approved and are being used as treatments, but it is unclear as to whether they are the most potent BMPs that induce bone formation. According to recent studies, BMP-9 is known to be the most potent inducer of the osteogenic differentiation of mesenchymal stem cells, both in vitro and in vivo. However, its exact role in the skeletal system is still unclear. In addition, research results suggest that the molecular mechanism of BMP-9-mediated bone formation is also different from the previously known BMP family, suggesting that research on signaling pathways related to BMP-9-mediated bone formation is actively being conducted. In this study, we performed a phosphorylation array to investigate the signaling mechanism of BMP-9 compared with BMP-2, another influential bone-forming growth factor, and we compared the downstream signaling system. We present a mechanism for the signal transduction of BMP-9, focusing on the previously known pathway and the p53 factor, which is relatively upregulated compared with BMP-2. |
first_indexed | 2024-03-10T21:11:59Z |
format | Article |
id | doaj.art-a4d6f1261eb44ad587d1adf97cfbc38d |
institution | Directory Open Access Journal |
issn | 1661-6596 1422-0067 |
language | English |
last_indexed | 2024-03-10T21:11:59Z |
publishDate | 2023-10-01 |
publisher | MDPI AG |
record_format | Article |
series | International Journal of Molecular Sciences |
spelling | doaj.art-a4d6f1261eb44ad587d1adf97cfbc38d2023-11-19T16:43:57ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672023-10-0124201525210.3390/ijms242015252BMP-9 Improves the Osteogenic Differentiation Ability over BMP-2 through p53 Signaling In Vitro in Human Periosteum-Derived CellsJin-Ho Park0Eun-Byeol Koh1Young-Jin Seo2Hye-Seong Oh3June-Ho Byun4Department of Nutritional Science, University of Michigan School of Public Health, Ann Arbor, MI 48109, USADepartment of Oral and Maxillofacial Surgery, Gyeongsang National University School of Medicine, Gyeongsang National University Hospital, Institute of Medical Sciences, Gyeongsang National University, Jinju 52727, Republic of KoreaDepartment of Oral and Maxillofacial Surgery, Gyeongsang National University School of Medicine, Gyeongsang National University Hospital, Institute of Medical Sciences, Gyeongsang National University, Jinju 52727, Republic of KoreaDepartment of Oral and Maxillofacial Surgery, Gyeongsang National University School of Medicine, Gyeongsang National University Hospital, Institute of Medical Sciences, Gyeongsang National University, Jinju 52727, Republic of KoreaDepartment of Oral and Maxillofacial Surgery, Gyeongsang National University School of Medicine, Gyeongsang National University Hospital, Institute of Medical Sciences, Gyeongsang National University, Jinju 52727, Republic of KoreaBone morphogenetic proteins (BMPs) have tremendous therapeutic potential regarding the treatment of bone and musculoskeletal disorders due to their osteo-inductive ability. More than twenty BMPs have been identified in the human body with various functions, such as embryonic development, skeleton genesis, hematopoiesis, and neurogenesis. BMPs can induce the differentiation of MSCs into the osteoblast lineage and promote the proliferation of osteoblasts and chondrocytes. BMP signaling is also involved in tissue remodeling and regeneration processes to maintain homeostasis in adults. In particular, growth factors, such as BMP-2 and BMP-7, have already been approved and are being used as treatments, but it is unclear as to whether they are the most potent BMPs that induce bone formation. According to recent studies, BMP-9 is known to be the most potent inducer of the osteogenic differentiation of mesenchymal stem cells, both in vitro and in vivo. However, its exact role in the skeletal system is still unclear. In addition, research results suggest that the molecular mechanism of BMP-9-mediated bone formation is also different from the previously known BMP family, suggesting that research on signaling pathways related to BMP-9-mediated bone formation is actively being conducted. In this study, we performed a phosphorylation array to investigate the signaling mechanism of BMP-9 compared with BMP-2, another influential bone-forming growth factor, and we compared the downstream signaling system. We present a mechanism for the signal transduction of BMP-9, focusing on the previously known pathway and the p53 factor, which is relatively upregulated compared with BMP-2.https://www.mdpi.com/1422-0067/24/20/15252BMP-9p53PI3K/AKTperiosteum-derived cellsosteogenic differentiation |
spellingShingle | Jin-Ho Park Eun-Byeol Koh Young-Jin Seo Hye-Seong Oh June-Ho Byun BMP-9 Improves the Osteogenic Differentiation Ability over BMP-2 through p53 Signaling In Vitro in Human Periosteum-Derived Cells International Journal of Molecular Sciences BMP-9 p53 PI3K/AKT periosteum-derived cells osteogenic differentiation |
title | BMP-9 Improves the Osteogenic Differentiation Ability over BMP-2 through p53 Signaling In Vitro in Human Periosteum-Derived Cells |
title_full | BMP-9 Improves the Osteogenic Differentiation Ability over BMP-2 through p53 Signaling In Vitro in Human Periosteum-Derived Cells |
title_fullStr | BMP-9 Improves the Osteogenic Differentiation Ability over BMP-2 through p53 Signaling In Vitro in Human Periosteum-Derived Cells |
title_full_unstemmed | BMP-9 Improves the Osteogenic Differentiation Ability over BMP-2 through p53 Signaling In Vitro in Human Periosteum-Derived Cells |
title_short | BMP-9 Improves the Osteogenic Differentiation Ability over BMP-2 through p53 Signaling In Vitro in Human Periosteum-Derived Cells |
title_sort | bmp 9 improves the osteogenic differentiation ability over bmp 2 through p53 signaling in vitro in human periosteum derived cells |
topic | BMP-9 p53 PI3K/AKT periosteum-derived cells osteogenic differentiation |
url | https://www.mdpi.com/1422-0067/24/20/15252 |
work_keys_str_mv | AT jinhopark bmp9improvestheosteogenicdifferentiationabilityoverbmp2throughp53signalinginvitroinhumanperiosteumderivedcells AT eunbyeolkoh bmp9improvestheosteogenicdifferentiationabilityoverbmp2throughp53signalinginvitroinhumanperiosteumderivedcells AT youngjinseo bmp9improvestheosteogenicdifferentiationabilityoverbmp2throughp53signalinginvitroinhumanperiosteumderivedcells AT hyeseongoh bmp9improvestheosteogenicdifferentiationabilityoverbmp2throughp53signalinginvitroinhumanperiosteumderivedcells AT junehobyun bmp9improvestheosteogenicdifferentiationabilityoverbmp2throughp53signalinginvitroinhumanperiosteumderivedcells |