Cyclase-associated protein 2 (CAP2) is a synaptic actin-binding protein involved in cofilin-mediated spine remodelling, Alzheimer’s Disease synaptic failure and myofibril maintenance, indicating its potential involvement in motor neuron disease (MND). This study examined cerebrospinal fluid (CSF) levels of CAP2 in 60 patients with MND and 40 healthy controls (HC) to assess its diagnostic and prognostic value and its relationship with neuronal, glial and synaptic markers. Glial fibrillary acidic protein (GFAP), neurofilament light chain (NfL), phosphorylated and total tau (p-Tau 181, t-Tau), CAP2 and synaptosomal-associated protein 25 (SNAP-25) were quantified using ELISA, Lumipulse and SIMOA platforms. MND patients displayed increased GFAP, NfL, t-Tau, p-Tau 181 levels and CAP2 while SNAP-25 was reduced. CAP2 correlated with tau markers, but not with NfL or GFAP. Unlike NfL, which was higher in upper motor neuron–predominant cases and predicted faster progression and poorer survival, CAP2 did not vary with disease subtypes or severity. The study showed that CAP2 is associated with MND independently from neuronal, glial and presynaptic dysfunction. Integrating CAP2 into multi-marker panels could enhance understanding of synaptic pathology in MND.

Synaptic and cytoskeletal CSF signatures of motor neuron disease: the role of cyclase-associated protein 2 / A. Pilotto, S.P.. - In: SCIENTIFIC REPORTS. - ISSN 2045-2322. - 16:1(2026 Feb 16), pp. 8703.1-8703.8. [10.1038/s41598-026-39274-0]

Synaptic and cytoskeletal CSF signatures of motor neuron disease: the role of cyclase-associated protein 2

S. Pelucchi
Co-primo
;
F. Gorla;L. D'Andrea;R. Stringhi;M. Di Luca;E. Marcello
Co-ultimo
;
2026

Abstract

Cyclase-associated protein 2 (CAP2) is a synaptic actin-binding protein involved in cofilin-mediated spine remodelling, Alzheimer’s Disease synaptic failure and myofibril maintenance, indicating its potential involvement in motor neuron disease (MND). This study examined cerebrospinal fluid (CSF) levels of CAP2 in 60 patients with MND and 40 healthy controls (HC) to assess its diagnostic and prognostic value and its relationship with neuronal, glial and synaptic markers. Glial fibrillary acidic protein (GFAP), neurofilament light chain (NfL), phosphorylated and total tau (p-Tau 181, t-Tau), CAP2 and synaptosomal-associated protein 25 (SNAP-25) were quantified using ELISA, Lumipulse and SIMOA platforms. MND patients displayed increased GFAP, NfL, t-Tau, p-Tau 181 levels and CAP2 while SNAP-25 was reduced. CAP2 correlated with tau markers, but not with NfL or GFAP. Unlike NfL, which was higher in upper motor neuron–predominant cases and predicted faster progression and poorer survival, CAP2 did not vary with disease subtypes or severity. The study showed that CAP2 is associated with MND independently from neuronal, glial and presynaptic dysfunction. Integrating CAP2 into multi-marker panels could enhance understanding of synaptic pathology in MND.
Cerebrospinal fluid (CSF); Motor neuron disease (MND); Neurofilament light chain (NfL); Synaptic biomarkers
Settore BIOS-11/A - Farmacologia
Settore MEDS-12/A - Neurologia
   Identification and validation of COmmon pathways at the CrOssrOads of neurodegeneration and Neuroprotection (COCOON)
   COCOON
   MINISTERO DELL'ISTRUZIONE E DEL MERITO
   2017MYJ5TH_001

   Soma TO syNapsE: the inverse communication ruling plasticity at specific synapses (STONE)
   STONE
   MINISTERO DELL'UNIVERSITA' E DELLA RICERCA
   FIS00000560

   Identification and validation of COmmon pathways at the CrOssrOads of neurodegeneration and Neuroprotection (COCOON)
   COCOON
   MINISTERO DELL'ISTRUZIONE E DEL MERITO
   2017MYJ5TH_001
16-feb-2026
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1249918
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