Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/75107

TítuloA biocompatible and injectable hydrogel to boost the efficacy of stem cells in neurodegenerative diseases treatment
Autor(es)Ferreira, Helena Susana Costa Machado
Amorim, Diana
Lima, Ana Cláudia Fernandes
Pirraco, Rogério P.
Pinto, Ana Rita Costa
Almeida, Rui
Almeida, Armando
Reis, R. L.
Pinto-Ribeiro, Filipa
Neves, N. M.
Palavras-chaveBone marrow mesenchymal stem cells
CNS delivery
Experimental autoimmune encephalomyelitis rat model
Hydrogel
Multiple sclerosis
Neurodegenerative diseases
Experimental autoimmune encephalomyelitis
rat model
DataOut-2021
EditoraElsevier
RevistaLife Sciences
CitaçãoFerreira H., Amorim D., Lima Ana C., Pirraco R. P., Costa-Pinto A. R., Almeida R., Almeida A., Reis R. L., Pinto-Ribeiro F., Neves N. M. A biocompatible and injectable hydrogel to boost the efficacy of stem cells in neurodegenerative diseases treatment, Life Sciences, Vol. 287, pp. 120108, doi:10.1016/j.lfs.2021.120108, 2021
Resumo(s)Aims: Stem cell therapies emerged as treatment modalities with potential to cure neurodegenerative diseases (NDs). However, despite high expectations, their clinical use is still limited. Critical issues in treatment outcomes may be related to stem cells formulation and administration route. We develop a hydrogel as a cell carrier, consisting of compounds (phospholipids and hyaluronic acid-HA) naturally present in the central nervous system (CNS). The HA-based hydrogel physically crosslinked with liposomes is designed for direct injection into the CNS to significantly increase the bone marrow mesenchymal stem cells (BMSCs) bioavailability. Materials and methods: Hydrogel compatibility is confirmed in vitro with BMSCs and in vivo through its intracerebroventricular injection in rats. To assess its efficacy, the main cause of chronic neurologic disability in young adults is selected, namely multiple sclerosis (MS). The efficacy of the developed formulation containing a lower number of cells than previously reported is demonstrated using an experimental autoimmune encephalomyelitis (EAE) rat model. Key findings: The distribution of the engineered hydrogel into corpus callosum can be ideal for NDs treatment, since damage of this white matter structure is responsible for important neuronal deficits. Moreover, the BMSCs laden hydrogel significantly decreases disease severity and maximum clinical score and eliminated the relapse. Significance: The engineering of advanced therapies using this natural carrier can result in efficacious treatmentsfor MS and related debilitating conditions.
TipoArtigo
URIhttps://hdl.handle.net/1822/75107
DOI10.1016/j.lfs.2021.120108
ISSN0024-3205
Versão da editorahttps://pubmed.ncbi.nlm.nih.gov/34717909/
Arbitragem científicayes
AcessoAcesso restrito UMinho
Aparece nas coleções:3B’s - Artigos em revistas/Papers in scientific journals

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