Alejandro Gella

Dr. Alejandro Gella

orcid

Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2009 in Cell Adhesion & Migration
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Journal Article
Closed access
AGAlejandro Gella
Alejandro Gella
NDNuria Durany
Nuria Durany
Alzheimer disease (AD) is a progressive dementia affecting a large proportion of the aging population. The histopathological changes in AD include neuronal cell death, formation of amyloid plaques ...

1 January 2010 in Neurobiology of Disease
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Journal Article
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TVTony Valente
Tony Valente
AGAlejandro Gella
Alejandro Gella
Xavier Fernàndez-BusquetsXavier Fernàndez-Busquets
Xavier Fernàndez-Busquets
MUMercedes Unzeta
Mercedes Unzeta
NDNuria Durany
Nuria Durany

13 December 2012 in Journal of Neural Transmission
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Journal Article
Closed access
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IBIrene Bolea
Irene Bolea
AGAlejandro Gella
Alejandro Gella
MUMercedes Unzeta
Mercedes Unzeta

22 September 2011 in Biomacromolecules
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Journal Article
Closed access
Oxana KlementievaOxana Klementieva
Oxana Klementieva
NBNuria Benseny-Cases
Nuria Benseny-Cases
AGAlejandro Gella
Alejandro Gella
DADietmar Appelhans
Dietmar Appelhans
BVBrigitte Voit
Brigitte Voit
JCJosep Cladera
Josep Cladera

12 August 2019 in eLife
Verified
Journal Article
Open access
IBIrene Bolea
Irene Bolea
AGAlejandro Gella
Alejandro Gella
ESElisenda Sanz
Elisenda Sanz
PPPatricia Prada-Dacasa
Patricia Prada-Dacasa
FMFabien Menardy
Fabien Menardy
Albert QuintanaAlbert Quintana
Albert Quintana
Mitochondrial deficits in energy production cause untreatable and fatal pathologies known as mitochondrial disease (MD). Central nervous system affectation is critical in Leigh Syndrome (LS), a common MD presentation, leading to motor and respiratory deficits, seizures and premature death. However, only specific neuronal populations are affected. Furthermore, their molecular identity and their contribution to the disease remains unknown. Here, using a mouse model of LS lacking the mitochondrial complex I subunit Ndufs4, we dissect the critical role of genetically-defined neuronal populations in LS progression. Ndufs4 inactivation in Vglut2-expressing glutamatergic neurons leads to decreased neuronal firing, brainstem inflammation, motor and respiratory deficits, and early death. In contrast, Ndufs4 deletion in GABAergic neurons causes basal ganglia inflammation without motor or respiratory involvement, but accompanied by hypothermia and severe epileptic seizures preceding death. These results provide novel insight in the cell type-specific contribution to the pathology, dissecting the underlying cellular mechanisms of MD.

4 September 2024 in Nature Communications
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Journal Article
Open access
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EPEmma Puighermanal
Emma Puighermanal
MLMarta Luna-Sánchez
Marta Luna-Sánchez
AGAlejandro Gella
Alejandro Gella
GWGunter van der Walt
Gunter van der Walt
AUAndrea Urpi
Andrea Urpi
Albert QuintanaAlbert Quintana
Albert Quintana
Mutations in mitochondrial energy-producing genes lead to a heterogeneous group of untreatable disorders known as primary mitochondrial diseases (MD). Leigh syndrome (LS) is the most common pediatric MD and is characterized by progressive neuromuscular affectation and premature death. Here, we show that daily cannabidiol (CBD) administration significantly extends lifespan and ameliorates pathology in two LS mouse models, and improves cellular function in fibroblasts from LS patients. CBD delays motor decline and neurodegenerative signs, improves social deficits and breathing abnormalities, decreases thermally induced seizures, and improves neuropathology in affected brain regions. Mechanistically, we identify peroxisome proliferator-activated receptor gamma (PPARγ) as a key nuclear receptor mediating CBD’s beneficial effects, while also providing proof of dysregulated PPARγ expression and activity as a common feature in both mouse neurons and fibroblasts from LS patients. Taken together, our results provide the first evidence for CBD as a potential treatment for LS.