Identification of a Novel Osteogenetic Oligodeoxynucleotide (osteoDN) That Promotes Osteoblast Differentiation in a TLR9-Independent Manner

Bibliographic Details
Title: Identification of a Novel Osteogenetic Oligodeoxynucleotide (osteoDN) That Promotes Osteoblast Differentiation in a TLR9-Independent Manner
Authors: Yuma Nihashi, Mana Miyoshi, Koji Umezawa, Takeshi Shimosato, Tomohide Takaya
Source: Nanomaterials, Vol 12, Iss 10, p 1680 (2022)
Publisher Information: MDPI AG, 2022.
Publication Year: 2022
Collection: LCC:Chemistry
Subject Terms: osteogenetic oligodeoxynucleotide (osteoDN), osteoblast, bone differentiation, calcification, mineralization, Toll-like receptor 9 (TLR9), Chemistry, QD1-999
More Details: Dysfunction of bone-forming cells, osteoblasts, is one of the causes of osteoporosis. Accumulating evidence has indicated that oligodeoxynucleotides (ODNs) designed from genome sequences have the potential to regulate osteogenic cell fate. Such osteogenetic ODNs (osteoDNs) targeting and activating osteoblasts can be the candidates of nucleic acid drugs for osteoporosis. In this study, the ODN library derived from the Lacticaseibacillus rhamnosus GG genome was screened to determine its osteogenetic effect on murine osteoblast cell line MC3T3-E1. An 18-base ODN, iSN40, was identified to enhance alkaline phosphatase activity of osteoblasts within 48 h. iSN40 also induced the expression of osteogenic genes such as Msx2, osterix, collagen type 1α, osteopontin, and osteocalcin. Eventually, iSN40 facilitated calcium deposition on osteoblasts at the late stage of differentiation. Intriguingly, the CpG motif within iSN40 was not required for its osteogenetic activity, indicating that iSN40 functions in a TLR9-independent manner. These data demonstrate that iSN40 serves as a novel osteogenetic ODN (osteoDN) that promotes osteoblast differentiation. iSN40 provides a potential seed of the nucleic acid drug that activating osteoblasts for osteoporosis therapy.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 12101680
2079-4991
Relation: https://www.mdpi.com/2079-4991/12/10/1680; https://doaj.org/toc/2079-4991
DOI: 10.3390/nano12101680
Access URL: https://doaj.org/article/c126998845944ec3800f5e9de803d5e7
Accession Number: edsdoj.126998845944ec3800f5e9de803d5e7
Database: Directory of Open Access Journals
More Details
ISSN:12101680
20794991
DOI:10.3390/nano12101680
Published in:Nanomaterials
Language:English