: Heparin and heparan sulfate (HS) glycosaminoglycans (GAGs) are essential regulators of neurotrophic signaling. However, their therapeutic applications are hindered by structural heterogeneity, batch variability, and anticoagulant activity. Thus, there is a need for well-defined glycomimetics that replicate the function of native HS in regenerative medicine. Here, we synthesized HS glycomimetics through a modular strategy that enables the installation of sulfate groups at the designated positions along the sugar backbone. These glycomimetics selectively bind and stabilize neurotrophins, such as fibroblast growth factors (FGF-1, FGF-2) and nerve growth factor (NGF), in a sulfation-dependent manner with dissociation constants in the low micromolar range. They exhibit no anticoagulant activity, a crucial prerequisite for clinical translation. We show that our lead compound has neuritogenic ability because in two neuronal cell models, PC12 and SH-SY5Y, it enhances NGF-mediated neural maturation when immobilized on a surface. Furthermore, in primary rat hippocampal neurons, it promotes FGF-2-mediated neurite outgrowth and spontaneous synaptic activity. Our findings show that HS glycomimetics have the potential for regenerative therapies.

Unraveling the Potential of Small Molecule Heparin Glycomimetics in Neuroregenerative Therapeutics / Özkan, Melis; Cellot, Giada; Pawar, Sujeet; Sardana, Deepika; Barravecchia, Ivana; Ballerini, Laura; Angeloni, Debora; Micera, Silvestro; Stellacci, Francesco. - In: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. - ISSN 0002-7863. - 147:50(2025), pp. ---. [10.1021/jacs.5c13142]

Unraveling the Potential of Small Molecule Heparin Glycomimetics in Neuroregenerative Therapeutics

Giada Cellot
Secondo
;
Laura Ballerini;Francesco Stellacci
2025-01-01

Abstract

: Heparin and heparan sulfate (HS) glycosaminoglycans (GAGs) are essential regulators of neurotrophic signaling. However, their therapeutic applications are hindered by structural heterogeneity, batch variability, and anticoagulant activity. Thus, there is a need for well-defined glycomimetics that replicate the function of native HS in regenerative medicine. Here, we synthesized HS glycomimetics through a modular strategy that enables the installation of sulfate groups at the designated positions along the sugar backbone. These glycomimetics selectively bind and stabilize neurotrophins, such as fibroblast growth factors (FGF-1, FGF-2) and nerve growth factor (NGF), in a sulfation-dependent manner with dissociation constants in the low micromolar range. They exhibit no anticoagulant activity, a crucial prerequisite for clinical translation. We show that our lead compound has neuritogenic ability because in two neuronal cell models, PC12 and SH-SY5Y, it enhances NGF-mediated neural maturation when immobilized on a surface. Furthermore, in primary rat hippocampal neurons, it promotes FGF-2-mediated neurite outgrowth and spontaneous synaptic activity. Our findings show that HS glycomimetics have the potential for regenerative therapies.
2025
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11368/3122065
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