VEGFR1PRIMES A UNIQUE COHORT OF DENTAL PULP STEM CELLS FOR VASCULOGENIC DIFFERENTIATION

Author(s)

Bergamo, M. T. ^{[1, 2]} ; Zhang, Z. ^[2] ; Oliveira, T. M. ^[1] ; Nor, J. E. ^[2]

Affiliation

^[1] Univ Sao Paulo, Bauru Sch Dent, Dept Pediat Dent Orthodont & Collect Hlth, Bauru, SP - Brazil

^[2] Univ Michigan, Sch Dent, Dept Cariol Restorat Sci & Endodont, 1011 N Univ Rm G049, Ann Arbor, MI 48109 - USA

• Document type: Journal article
• Source: EUROPEAN CELLS & MATERIALS; v. 41, p. 332-344, JAN-JUN 2021.
• Web of Science Citations: 0

Abstract

Dental pulp stem cells (DPSCs) constitute a unique group of cells endowed with multipotency, self-renewal, and capacity to regenerate the dental pulp tissue. While much has been learned about these cells in recent years, it is still unclear if each DPSC is multipotent or if unique sub-populations of DPSCs are ``primed{''} to undergo specific differentiation paths. The purpose of the present study was to define whether a subpopulation of DPSCs was uniquely primed to undergo vasculogenic differentiation. Permanent-tooth DPSCs or stem cells from human exfoliated deciduous teeth (SHED) were flow-sorted for vascular endothelial growth factor receptor I (VEGFR1) and exposed to vasculogenic differentiation medium, i.e., Microvascular Endothelial Cell Growth Medium-2 BulletKit (TM) supplemented with 50 ng/mL rhVEGF(165) in the presence of 0 or 25 mu g/mL anti-human VEGF antibody (bevacizumab; Genentech). In addition, sorted SHED (i.e., VEGFR1(high) or VEGFR1(low)) were seeded in biodegradable scaffolds and transplanted into the subcutaneous space of immunodeficient mice. Despite proliferating at a similar rate, VEGFR1(high) generated more in vitro sprouts than VEGFR1(low) cells (p < 0.05). Blockade of VEGF signaling with bevacizumab inhibited VEGFR1(high)-derived sprouts, demonstrating specificity of responses. Similarly, VEGFR1(high) SHED generated more blood vessels when transplanted into murine hosts than VEGFR1(low) cells (p < 0.05). Collectively, these data demonstrated that DPSCs contain a unique sub-population of cells defined by high VEGFR1 expression that are primed to differentiate into vascular endothelial cells. These data raise the possibility of purifying stem cells with high vasculogenic potential for regeneration of vascularized tissues or for vascular engineering in the treatment of ischemic conditions. (AU)

• FAPESP's process: 18/13675-0 - Dental pulp stem cell biology
• Grantee: Mariel Tavares de Oliveira Prado Bergamo
• Support Opportunities: Scholarships abroad - Research Internship - Doctorate