Sel Punca Adiposa Sebagai Alternatif Terapi Penyakit Neurodegeneratif

Lathifah Yasmine Wulandari

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Terapi dengan sel punca adiposa dapat mengisi sel yang hilang dan melindungi area di bawah proses kerusakan degeneratif saraf. Terapi sel punca ini diharapkan dapat dipertimbangkan sebagai potensi dan mengurangi manifestasi klinis  pada penyakit neurodegeneratif. Tujuan artikel ini untuk mengetahui potensi dan fungsi terapi sel punca adiposa sebagai salah satu terapi alternatif untuk penyakit neurodegeneratifArtikel dibuat dengan metode literature review, melibatkan 37 pustaka yang berupa buku dan jurnal internasional. Sel punca adiposa bersifat totipoten (dapat menjadi berbagai jenis sel) sehingga dapat menggantikan sel saraf yang rusak. Selain itu, sel punca adiposa mengekspresikan protein seperti NGF (nerve growth factor), brain-derived neurotrophic factor (BDNF), PGC1a (proliferator-activated receptor-g coactivator 1a), Neuro2A, VEGF (Vascular endothel growth factor) dan HGF (hepatocyte growth factor) yang mendorong regenerasi neurit, mengurangi inflamasi, memicu pembentukan jaringan baru dan bersifat neuroprotektif..                                                                                  Berdasarkan studi literatur disimpulkan bahwa sel punca adiposa merupakan sel yang baik untuk terapi penyakit neurodegeneratif.


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Bourin P et al., 2013. Stromal cells from the adipose tissue-derived stromal vascular fraction and culture expanded adipose tissue-derived stromal/stem cells: A joint statement of the International Federation for Adipose Therapeutics and Science (IFATS) and the International Society for Cellular Therapy(ISCT) Cytotherapy. 2013;15:641–648

Chan et al., 2014. ADSC Therapy in Neurodegenerative Disorders. Cell Transplantation, Vol. 23, pp. 549–557, 2014

Chivet et al., 2013.Exosomes as a novel way of interneuronal communication. Biochem. Soc. Trans. 41(1):241–244; 2013.

Chu et al., 2019. Adipose Tissue Stem Cells for Therapy: An Update on the Progress of Isolation, Culture, Storage, and Clinical Application. Cell. Biochem. 98(5):1076–1084

Chun et al., 2019. Preparation and Characterization of Human Adipose Tissue-Derived Extra-cellular Matrix, Growth Factors, and Stem Cells: A Concise Review. Tissue Eng Regen Med. 2019 Jul 5;16 (4):385-393.

Clarke et al., 2011. Stem Cell Growth and Differentiation. Tocris Scientific Review Series; Biological Sciences and Department of Chemistry, Durham University.

de la Cruz, Pérez . Effectiveness of aquatic therapy for the control of pain and increased functionality in people with-Parkinson's- disease: a random-ized clinical trial. Eur J Phys Rehabil Med. 2017 Dec-;53(6):825-832. 2017

Faust et al., 2009. Neuroprotective effects of compounds with antioxidant and anti-inflammatory properties in a Drosophila model of Parkinson’s disease. BMC Neurosci. 10:109; 2009.

Fedorova, et al., 2011. Levodopa medications in the treatment of Parkinson’s disease]. Zh. Nevrol. Psikhiatr. Im. S. S. Korsakova 111(5):30–36.

Ferraiuolo et al., 2011. Molecular pathways of motor neuron injury in amyotrophic lateral sclerosis. Nat. Rev. Neurol. 7(11):616– 630.

Glascock et al., 2013. Delivery of therapeutic agents through intracerebroventricular (ICV) and intravenous (IV) injection in mice. J. Vis. Exp. 56:2968

Gu et al., 2013. Adipose stromal cells-conditioned medium blocks 6- hydroxydopamine-induced neurotoxicity and reactive oxygen species. Neurosci. Lett. 544:15–19.

Gutierrez-Fernandez et al, 2013. Adipose tissue- derived stem cells in stroke treatment: from bench to bedside. Discov Med. 2013 Aug;16:37–43.

Gutiérrez-Fernández et al., 2015. Comparison between xenogeneic and allogeneic adipose mesenchymal stem cells in the treatment of acute cerebral infarct: proof of concept in rats. Journal of translational medicine. 2015;13:46.

Gombash et al., 2012. Striatal pleiotrophin overexpression provides functional and morphological neuroprotection in the 6-hydroxydopamine model. Mol. Ther. 20(3):544–554.

Ikegame et al., 2011. Comparison of mesenchymal stem cells from adipose tissue and bone marrow for ischemic stroke therapy. Cytotherapy. 2011;13:675–685.

Im, W et al., 2013. Extracts of adipose derived stem cells slows progression In the R6/2 Model of Huntington’s disease. PLoS One 8(4):e59438.

Jeon et al., 2013. Transplantation of Neuro2a Cells into the Developing Postnatal Mouse Eye. Acta Histochem Cytochem. 2015 Dec 25;48(6):205-14.

Jones et al., 2012. Human adipose stem cell-conditioned medium increases survival of Friedreich’s ataxia cells submitted to oxidative stress. Stem Cells Dev. 21(15):2817–2826.

Jucker dan Walker et al., 2013. Self-propagation of pathogenic protein aggregates in neurodegenerative diseases. Nature 501(7465):45–51.

Kalia et al., 2013. alpha-Synuclein oligomers and clinical implications Parkinson disease. Ann. Neurol. 73(2):155–169.

Kalra dan Tomar. 2014. Stem Cell: Basics, Classification and Applications. American Journal of Phytomedicine and Clinical Therapeutics :ISSN 2321 – 2748.

Kim et al., 2012. The preventive and therapeutic effects of intravenous human adipose-derived stem cells in Alzheimer’s disease mice. PLoS One 7(9):e45757.

Liu et al., 2013. Stem cell applic-ations in regenerative medicine for neurological disorders. Cell Transplantion Journal. 22(4):631–637.

Ma et al., 2013. Intracerebral transplantation of adipose-derived mesenchymal stem cells alternatively activates microglia and ameliorates neuro-pathological deficits in Alzheimer’s disease mice. Cell Transplant. 22(S1):113–126.

Maucksch, C et al., 2013. Stem cell-based therapy for Huntington’s disease. J. Cell. Biochem. 114(4):754–763.

Moriyama et al., 2012. Human adipose tissue-derived multilineage progenitor cells exposed to oxidative stress induce neurite outgrowth in PC12 cells through p38 MAPK signaling. BMC Cell Biol. 13:21.

Pérez-González et al., 2011. Leptin induces proliferation of neuronal progenitors and neuroprotection in a mouse model of Alzheimer’s disease. J.Alzheimers Dis. 24(Suppl 2):17–25.

Roos, R. A. 2010. Huntington’s disease: A clinical review. Orphanet J. Rare Dis. 5(1):40.

Sabol et al., 2018. Therapeutic Potential of Adipose Stem Cells. Adv. Exp. Med. Biol. 2018

Subramaniam et al., 2009. Rhes, a striatal specific protein, mediates mutant-huntingtin cytotoxicity. Science 324(5932):1327–1330;

Talbott et al., 2016. The epidemiology of amyotrophic lateral sclerosis. Pittsburg : Handb Clin Neurol .2016;138:225-38

Tanzi, R. E .2013. A brief history of Alzheimer’s disease gene dis- covery. J. Alzheimers Dis. 33(Suppl 1):S5–S13.

Torrent dan Polli, 2018. Mesenchymal stem cell transplantation for neuro-degenerative diseases. Cell Transplant.Journal 17(10–11): 1103–1113.

van der Marck et al. 2009. Multidisciplinary care for patients with Parkinson’s disease. Parkinsonism Relat. Disord. 15(Sup3):S219–S223

Zhou et al., 2013. Recovery of behavioral symptoms in hemi-parkinsonian rhesus monkeys through combined gene and stem cell therapy.Cytotherapy 15(4):467–480.




DOI: https://doi.org/10.33024/jfm.v2i2.2221

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