FOROSTYAK, Serhij, O. FOROSTYAK, J. C. F. KWOK, N. ROMANYUK, Monika REHOROVA, Jan KRISKA, G. DAYANITHI, R. RAHA-CHOWDHURY, Pavla JENDELOVA, Miroslava ANDEROVA, J. W. FAWCETT a Eva SYKOVA. Transplantation of Neural Precursors Derived from Induced Pluripotent Cells Preserve Perineuronal Nets and Stimulate Neural Plasticity in ALS Rats. International Journal of Molecular Sciences. Basel: Multidisciplinary Digital Publishing Institute, 2020, roč. 21, č. 24, s. 1-25. ISSN 1422-0067. Dostupné z: https://dx.doi.org/10.3390/ijms21249593.
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Základní údaje
Originální název Transplantation of Neural Precursors Derived from Induced Pluripotent Cells Preserve Perineuronal Nets and Stimulate Neural Plasticity in ALS Rats
Autoři FOROSTYAK, Serhij (203 Česká republika, garant, domácí), O. FOROSTYAK, J. C. F. KWOK, N. ROMANYUK, Monika REHOROVA (203 Česká republika), Jan KRISKA (203 Česká republika), G. DAYANITHI, R. RAHA-CHOWDHURY, Pavla JENDELOVA (203 Česká republika), Miroslava ANDEROVA (203 Česká republika), J. W. FAWCETT a Eva SYKOVA (203 Česká republika).
Vydání International Journal of Molecular Sciences, Basel, Multidisciplinary Digital Publishing Institute, 2020, 1422-0067.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 10608 Biochemistry and molecular biology
Stát vydavatele Švýcarsko
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 5.923
Kód RIV RIV/00216224:14110/20:00117891
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.3390/ijms21249593
UT WoS 000603507100001
Klíčová slova anglicky proteoglycans; plasticity; neurodegeneration; stem cells; iPS; ALS; motoneuron death; transplantation
Štítky 14110229, rivok
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Mgr. Tereza Miškechová, učo 341652. Změněno: 21. 7. 2021 10:28.
Anotace
A promising therapeutic strategy for amyotrophic lateral sclerosis (ALS) treatment is stem cell therapy. Neural progenitors derived from induced pluripotent cells (NP-iPS) might rescue or replace dying motoneurons (MNs). However, the mechanisms responsible for the beneficial effect are not fully understood. The aim here was to investigate the mechanism by studying the effect of intraspinally injected NP-iPS into asymptomatic and early symptomatic superoxide dismutase (SOD)1(G93A) transgenic rats. Prior to transplantation, NP-iPS were characterized in vitro for their ability to differentiate into a neuronal phenotype. Motor functions were tested in all animals, and the tissue was analyzed by immunohistochemistry, qPCR, and Western blot. NP-iPS transplantation significantly preserved MNs, slowed disease progression, and extended the survival of all treated animals. The dysregulation of spinal chondroitin sulfate proteoglycans was observed in SOD1(G93A) rats at the terminal stage. NP-iPS application led to normalized host genes expression (versican, has-1, tenascin-R, ngf, igf-1, bdnf, bax, bcl-2, and casp-3) and the protection of perineuronal nets around the preserved MNs. In the host spinal cord, transplanted cells remained as progenitors, many in contact with MNs, but they did not differentiate. The findings suggest that NP-iPS demonstrate neuroprotective properties by regulating local gene expression and regulate plasticity by modulating the central nervous system (CNS) extracellular matrix such as perineuronal nets (PNNs).
VytisknoutZobrazeno: 27. 5. 2024 16:38