Nicotinamide Riboside Modulates HIF-1 Signaling to Maintain and Enhance Odontoblastic Differentiation in Human Dental Pulp Stem Cells
© The Author(s) 2023. Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissionsoup.com..
Human dental pulp stem cells (hDPSCs) play a vital role in the regeneration of the pulp-dentin complex after pulp disease. While the regeneration efficiency relies on the odontoblastic differentiation capacity of hDPSCs, this is difficult to regulate within the pulp cavity. Although nicotinamide riboside (NR) has been found to promote tissue regeneration, its specific role in pulp-dentin complex regeneration is not fully understood. Here, we aimed to explore the role of NR in the odontoblastic differentiation of hDPSCs and its underlying molecular mechanism. It was found that NR enhanced the viability and retarded senescence in hDPSCs with higher NAD+/NADH levels. In contrast to the sustained action of NR, the multi-directional differentiation of hDPSCs was enhanced after NR pre-treatment. Moreover, in an ectopic pulp regeneration assay in nude mice, transplantation of hDPSCs pretreated with NR promoted the formation of a dentin-like structure surrounded by cells positively expressing DMP-1 and DSPP. RNA-Seq demonstrated inhibition of the HIF-1 signaling pathway in hDPSCs pretreated with NR. The number of HIF-1α-positive cells was significantly decreased in hDPSCs pretreated by NR in vivo. Similarly, NR significantly downregulated the expression of HIF-1α in vitro. The findings suggested that NR could potentially regulate hDPSC odontoblastic differentiation and promote the development of innovative strategies for dental pulp repair.
Errataetall: | |
---|---|
Medienart: |
E-Artikel |
Erscheinungsjahr: |
2024 |
---|---|
Erschienen: |
2024 |
Enthalten in: |
Zur Gesamtaufnahme - volume:42 |
---|---|
Enthalten in: |
Stem cells (Dayton, Ohio) - 42(2024), 2 vom: 08. Feb., Seite 116-127 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Zhan, Peimeng [VerfasserIn] |
---|
Links: |
---|
Anmerkungen: |
Date Completed 16.02.2024 Date Revised 14.03.2024 published: Print ErratumIn: Stem Cells. 2023 Dec 30;:. - PMID 38158633 Citation Status MEDLINE |
---|
doi: |
10.1093/stmcls/sxad083 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM364437618 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | NLM364437618 | ||
003 | DE-627 | ||
005 | 20240314234641.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231226s2024 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1093/stmcls/sxad083 |2 doi | |
028 | 5 | 2 | |a pubmed24n1328.xml |
035 | |a (DE-627)NLM364437618 | ||
035 | |a (NLM)37952104 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Zhan, Peimeng |e verfasserin |4 aut | |
245 | 1 | 0 | |a Nicotinamide Riboside Modulates HIF-1 Signaling to Maintain and Enhance Odontoblastic Differentiation in Human Dental Pulp Stem Cells |
264 | 1 | |c 2024 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 16.02.2024 | ||
500 | |a Date Revised 14.03.2024 | ||
500 | |a published: Print | ||
500 | |a ErratumIn: Stem Cells. 2023 Dec 30;:. - PMID 38158633 | ||
500 | |a Citation Status MEDLINE | ||
520 | |a © The Author(s) 2023. Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissionsoup.com. | ||
520 | |a Human dental pulp stem cells (hDPSCs) play a vital role in the regeneration of the pulp-dentin complex after pulp disease. While the regeneration efficiency relies on the odontoblastic differentiation capacity of hDPSCs, this is difficult to regulate within the pulp cavity. Although nicotinamide riboside (NR) has been found to promote tissue regeneration, its specific role in pulp-dentin complex regeneration is not fully understood. Here, we aimed to explore the role of NR in the odontoblastic differentiation of hDPSCs and its underlying molecular mechanism. It was found that NR enhanced the viability and retarded senescence in hDPSCs with higher NAD+/NADH levels. In contrast to the sustained action of NR, the multi-directional differentiation of hDPSCs was enhanced after NR pre-treatment. Moreover, in an ectopic pulp regeneration assay in nude mice, transplantation of hDPSCs pretreated with NR promoted the formation of a dentin-like structure surrounded by cells positively expressing DMP-1 and DSPP. RNA-Seq demonstrated inhibition of the HIF-1 signaling pathway in hDPSCs pretreated with NR. The number of HIF-1α-positive cells was significantly decreased in hDPSCs pretreated by NR in vivo. Similarly, NR significantly downregulated the expression of HIF-1α in vitro. The findings suggested that NR could potentially regulate hDPSC odontoblastic differentiation and promote the development of innovative strategies for dental pulp repair | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a HIF-1 | |
650 | 4 | |a human dental pulp stem cells | |
650 | 4 | |a nicotinamide riboside | |
650 | 4 | |a odontoblastic differentiation | |
650 | 4 | |a regeneration | |
650 | 7 | |a Niacinamide |2 NLM | |
650 | 7 | |a 25X51I8RD4 |2 NLM | |
650 | 7 | |a nicotinamide-beta-riboside |2 NLM | |
650 | 7 | |a 0I8H2M0L7N |2 NLM | |
650 | 7 | |a Pyridinium Compounds |2 NLM | |
650 | 7 | |a HIF1A protein, human |2 NLM | |
700 | 1 | |a Zhang, Xinfang |e verfasserin |4 aut | |
700 | 1 | |a Xie, Zhuo |e verfasserin |4 aut | |
700 | 1 | |a Chen, Lingling |e verfasserin |4 aut | |
700 | 1 | |a Huang, Shuheng |e verfasserin |4 aut | |
700 | 1 | |a Huang, Qiting |e verfasserin |4 aut | |
700 | 1 | |a Lin, Zhengmei |e verfasserin |4 aut | |
700 | 1 | |a Wang, Runfu |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Stem cells (Dayton, Ohio) |d 1994 |g 42(2024), 2 vom: 08. Feb., Seite 116-127 |w (DE-627)NLM074655477 |x 1549-4918 |7 nnns |
773 | 1 | 8 | |g volume:42 |g year:2024 |g number:2 |g day:08 |g month:02 |g pages:116-127 |
856 | 4 | 0 | |u http://dx.doi.org/10.1093/stmcls/sxad083 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 42 |j 2024 |e 2 |b 08 |c 02 |h 116-127 |