Influence of 2-hydroxyethyl methacrylate (HEMA) exposure on angiogenic differentiation of dental pulp stem cells (DPSCs)

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • André Jochums
  • Joachim Volk
  • Renke Perduns
  • Melanie Plum
  • Peter Schertl
  • Athina Bakopoulou
  • Werner Geurtsen

Organisationseinheiten

Externe Organisationen

  • Medizinische Hochschule Hannover (MHH)
  • Aristotle University of Thessaloniki (A.U.Th.)
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Details

OriginalspracheEnglisch
Seiten (von - bis)534-546
Seitenumfang13
FachzeitschriftDental Materials
Jahrgang37
Ausgabenummer3
Frühes Online-Datum23 Feb. 2021
PublikationsstatusVeröffentlicht - März 2021

Abstract

OBJECTIVE: The angiogenic differentiation of dental pulp stem cells (DPSCs) is important for tissue homeostasis and wound healing. In this study the influence of 2-hydroxyethyl methacrylate (HEMA) on angiogenic differentiation was investigated.

METHODS: To evaluate HEMA effects on angiogenic differentiation, DPSCs were cultivated in angiogenic differentiation medium (ADM) in the presence or absence of non-toxic HEMA concentrations (0.1 mM and 0.5 mM). Subsequently, angiogenic differentiation was analyzed on the molecular level by qRT-PCR and protein profiler analyzes of angiogenic markers and flow cytometry of PECAM1. The influence of HEMA on angiogenic phenotypes was analyzed by cell migration and sprouting assays.

RESULTS: Treatment with 0.5 mM HEMA during differentiation can lead to a slight reduction of angiogenic markers on mRNA level. HEMA also seems to slightly reduce the quantity of angiogenic cytokines (not significant). However, these HEMA concentrations have no detectable influence on cell migration, the abundance of PECAM1 and the formation of capillaries. Higher concentrations caused primary cytotoxic effects in angiogenic differentiation experiments conducted for longer periods than 72 h.

SIGNIFICANCE: Non-cytotoxic HEMA concentrations seem to have a minor impact on the expression of angiogenic markers, essentially on the mRNA level, without affecting the angiogenic differentiation process itself on a detectable level.

ASJC Scopus Sachgebiete

Zitieren

Influence of 2-hydroxyethyl methacrylate (HEMA) exposure on angiogenic differentiation of dental pulp stem cells (DPSCs). / Jochums, André; Volk, Joachim; Perduns, Renke et al.
in: Dental Materials, Jahrgang 37, Nr. 3, 03.2021, S. 534-546.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Jochums A, Volk J, Perduns R, Plum M, Schertl P, Bakopoulou A et al. Influence of 2-hydroxyethyl methacrylate (HEMA) exposure on angiogenic differentiation of dental pulp stem cells (DPSCs). Dental Materials. 2021 Mär;37(3):534-546. Epub 2021 Feb 23. doi: 10.1016/j.dental.2020.12.008
Jochums, André ; Volk, Joachim ; Perduns, Renke et al. / Influence of 2-hydroxyethyl methacrylate (HEMA) exposure on angiogenic differentiation of dental pulp stem cells (DPSCs). in: Dental Materials. 2021 ; Jahrgang 37, Nr. 3. S. 534-546.
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title = "Influence of 2-hydroxyethyl methacrylate (HEMA) exposure on angiogenic differentiation of dental pulp stem cells (DPSCs)",
abstract = "OBJECTIVE: The angiogenic differentiation of dental pulp stem cells (DPSCs) is important for tissue homeostasis and wound healing. In this study the influence of 2-hydroxyethyl methacrylate (HEMA) on angiogenic differentiation was investigated.METHODS: To evaluate HEMA effects on angiogenic differentiation, DPSCs were cultivated in angiogenic differentiation medium (ADM) in the presence or absence of non-toxic HEMA concentrations (0.1 mM and 0.5 mM). Subsequently, angiogenic differentiation was analyzed on the molecular level by qRT-PCR and protein profiler analyzes of angiogenic markers and flow cytometry of PECAM1. The influence of HEMA on angiogenic phenotypes was analyzed by cell migration and sprouting assays.RESULTS: Treatment with 0.5 mM HEMA during differentiation can lead to a slight reduction of angiogenic markers on mRNA level. HEMA also seems to slightly reduce the quantity of angiogenic cytokines (not significant). However, these HEMA concentrations have no detectable influence on cell migration, the abundance of PECAM1 and the formation of capillaries. Higher concentrations caused primary cytotoxic effects in angiogenic differentiation experiments conducted for longer periods than 72 h.SIGNIFICANCE: Non-cytotoxic HEMA concentrations seem to have a minor impact on the expression of angiogenic markers, essentially on the mRNA level, without affecting the angiogenic differentiation process itself on a detectable level.",
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TY - JOUR

T1 - Influence of 2-hydroxyethyl methacrylate (HEMA) exposure on angiogenic differentiation of dental pulp stem cells (DPSCs)

AU - Jochums, André

AU - Volk, Joachim

AU - Perduns, Renke

AU - Plum, Melanie

AU - Schertl, Peter

AU - Bakopoulou, Athina

AU - Geurtsen, Werner

N1 - Funding Information: Our thanks are due to Ms. S. Taubeler-Gerling for her commitment and excellent technical assistance. This study was supported by a grant of the Deutsche Forschungsgemeinschaft /German National Science Foundation (DFG) ( GE 455/17-1 ).

PY - 2021/3

Y1 - 2021/3

N2 - OBJECTIVE: The angiogenic differentiation of dental pulp stem cells (DPSCs) is important for tissue homeostasis and wound healing. In this study the influence of 2-hydroxyethyl methacrylate (HEMA) on angiogenic differentiation was investigated.METHODS: To evaluate HEMA effects on angiogenic differentiation, DPSCs were cultivated in angiogenic differentiation medium (ADM) in the presence or absence of non-toxic HEMA concentrations (0.1 mM and 0.5 mM). Subsequently, angiogenic differentiation was analyzed on the molecular level by qRT-PCR and protein profiler analyzes of angiogenic markers and flow cytometry of PECAM1. The influence of HEMA on angiogenic phenotypes was analyzed by cell migration and sprouting assays.RESULTS: Treatment with 0.5 mM HEMA during differentiation can lead to a slight reduction of angiogenic markers on mRNA level. HEMA also seems to slightly reduce the quantity of angiogenic cytokines (not significant). However, these HEMA concentrations have no detectable influence on cell migration, the abundance of PECAM1 and the formation of capillaries. Higher concentrations caused primary cytotoxic effects in angiogenic differentiation experiments conducted for longer periods than 72 h.SIGNIFICANCE: Non-cytotoxic HEMA concentrations seem to have a minor impact on the expression of angiogenic markers, essentially on the mRNA level, without affecting the angiogenic differentiation process itself on a detectable level.

AB - OBJECTIVE: The angiogenic differentiation of dental pulp stem cells (DPSCs) is important for tissue homeostasis and wound healing. In this study the influence of 2-hydroxyethyl methacrylate (HEMA) on angiogenic differentiation was investigated.METHODS: To evaluate HEMA effects on angiogenic differentiation, DPSCs were cultivated in angiogenic differentiation medium (ADM) in the presence or absence of non-toxic HEMA concentrations (0.1 mM and 0.5 mM). Subsequently, angiogenic differentiation was analyzed on the molecular level by qRT-PCR and protein profiler analyzes of angiogenic markers and flow cytometry of PECAM1. The influence of HEMA on angiogenic phenotypes was analyzed by cell migration and sprouting assays.RESULTS: Treatment with 0.5 mM HEMA during differentiation can lead to a slight reduction of angiogenic markers on mRNA level. HEMA also seems to slightly reduce the quantity of angiogenic cytokines (not significant). However, these HEMA concentrations have no detectable influence on cell migration, the abundance of PECAM1 and the formation of capillaries. Higher concentrations caused primary cytotoxic effects in angiogenic differentiation experiments conducted for longer periods than 72 h.SIGNIFICANCE: Non-cytotoxic HEMA concentrations seem to have a minor impact on the expression of angiogenic markers, essentially on the mRNA level, without affecting the angiogenic differentiation process itself on a detectable level.

KW - Cell Differentiation

KW - Cells, Cultured

KW - Dental Pulp

KW - Methacrylates

KW - Stem Cells

KW - Migration

KW - Spheroid sprouting

KW - Angiogenic differentiation

KW - Dental material

KW - Gene expression

KW - Composite resin

KW - Proteome profiler

KW - HEMA

KW - Dental pulp stem cells

KW - Matrigel

UR - http://www.scopus.com/inward/record.url?scp=85100795758&partnerID=8YFLogxK

U2 - 10.1016/j.dental.2020.12.008

DO - 10.1016/j.dental.2020.12.008

M3 - Article

C2 - 33579530

VL - 37

SP - 534

EP - 546

JO - Dental Materials

JF - Dental Materials

SN - 0109-5641

IS - 3

ER -

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