Elevated calcium in α-Gal A (-/0) neurons suggests disrupted calcium homeostasis and potential cellular damage.

Ca²⁺ ATPase activity is reduced in α-Gal A (-/0) neurons, impairing calcium regulation and cellular function.

Lower PMCA activity and acidic pH in α-Gal A (-/0) neurons hinder calcium extrusion, causing cytosolic buildup.

Mitochondria in α-Gal A (-/0) neurons show poor calcium buffering, worsening calcium signaling homeostasis.

Impaired lysosomal function in α-Gal A (-/0) neurons disrupts autophagy and increases cellular stress.

Neuropathic pain is a hallmark symptom in Fabry disease (FD), a hereditary X-linked lysosomal storage disorder caused by a reduced activity of α-galactosidase A (α-Gal A). The α-Gal A deficiency results in the progressive accumulation of globotriaosylceramide (Gb3) and globotriaosylsphingosine (lyso-Gb3) in the body fluids and lysosomes of various cell types, including sensory ganglia. The FD neuropathy affects the small thinly myelinated Aδ fibers and unmyelinated C fibers leading to the loss of intra-epidermal neuronal terminations, along with altered thermal and mechanical perception. Lipid accumulation, such as Gb3 and lyso-Gb3, is implicated in various cellular dysfunctions, including the alteration of ionic currents. It has been shown that administration of Gb3 to human umbilical vein endothelial cells leads to the downregulation of the calcium (Ca2+)-activated K+ channel KCa3.1, whereas lyso-Gb3 evokes cytosolic Ca2+ transients and an enhancement of voltage-activated Ca2+ currents in murine dorsal root ganglia. Therefore, we examined the mechanism underlying Ca2+ regulation in primary afferent neurons from the α-Gal A (−/0) mouse model. The obtained results suggest that other transport proteins participate in Ca2+ homeostasis in FD and their dysfunction may be directly involved in nociception. In this context, plasma-membrane Ca2+ ATPases exhibited reduced activity in FD, leading to an increased resting [Ca2+]i in sensory neurons. The reduced activity was associated with a decrease of cytosolic pH which weakened the PMCA-dependent calcium extrusion. We finally evaluated the contribution of mitochondria to the Ca2+ signalling and we observed impairment of the mitochondrial buffer capacity, as well as dysfunctional mitochondria and enhanced autophagy/mitophagy. These findings provide a basis for future insights into the alterations of calcium signalling underlying the onset of neuropathic symptoms in FD.

Fabry disease

Neuropathic pain

Globotriaosylceramide (Gb3)

Mouse model α-gal a (−/0)

DRG neurons

Calcium ions

Mitochondrial calcium

Plasma membrane calcium ATPase (PMCA)

© 2025 The Authors. Published by Elsevier Inc.