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Sökning: WFRF:(Aguila Julio) > Spatial RNA Sequenc...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003828naa a2200505 4500
001oai:DiVA.org:su-197224
003SwePub
008210929s2021 | |||||||||||000 ||eng|
009oai:prod.swepub.kib.ki.se:147260202
024a https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-1972242 URI
024a https://doi.org/10.3389/fnmol.2021.6995622 DOI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1472602022 URI
040 a (SwePub)sud (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Aguila, Julio4 aut
2451 0a Spatial RNA Sequencing Identifies Robust Markers of Vulnerable and Resistant Human Midbrain Dopamine Neurons and Their Expression in Parkinson's Disease
264 c 2021-07-08
264 1b Frontiers Media SA,c 2021
338 a print2 rdacarrier
520 a Defining transcriptional profiles of substantia nigra pars compacta (SNc) and ventral tegmental area (VTA) dopamine neurons is critical to understanding their differential vulnerability in Parkinson's Disease (PD). Here, we determine transcriptomes of human SNc and VTA dopamine neurons using LCM-seq on a large sample cohort. We apply a bootstrapping strategy as sample input to DESeq2 and identify 33 stably differentially expressed genes (DEGs) between these two subpopulations. We also compute a minimal sample size for identification of stable DEGs, which highlights why previous reported profiles from small sample sizes display extensive variability. Network analysis reveal gene interactions unique to each subpopulation and highlight differences in regulation of mitochondrial stability, apoptosis, neuronal survival, cytoskeleton regulation, extracellular matrix modulation as well as synapse integrity, which could explain the relative resilience of VTA dopamine neurons. Analysis of PD tissues showed that while identified stable DEGs can distinguish the subpopulations also in disease, the SNc markers SLIT1 and ATP2A3 were down-regulated and thus appears to be biomarkers of disease. In summary, our study identifies human SNc and VTA marker profiles, which will be instrumental for studies aiming to modulate dopamine neuron resilience and to validate cell identity of stem cell-derived dopamine neurons.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Neurovetenskaper0 (SwePub)301052 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Neurosciences0 (SwePub)301052 hsv//eng
653 a human midbrain dopamine neurons
653 a spatial transcriptomics
653 a laser microdissection
653 a RNA sequencing
653 a substantia nigra compacta
653 a ventral tegmental area
653 a Parkinson's disease
700a Cheng, Shangli4 aut
700a Kee, Nigelu Stockholms universitet,Institutionen för biokemi och biofysik,Karolinska Institutet, Sweden4 aut0 (Swepub:su)nike0958
700a Cao, Ming4 aut
700a Wang, Menghan4 aut
700a Deng, Qiaolinu Karolinska Institutet4 aut
700a Hedlund, Evau Stockholms universitet,Institutionen för biokemi och biofysik,Karolinska Institutet, Sweden4 aut0 (Swepub:su)evhe5970
710a Stockholms universitetb Institutionen för biokemi och biofysik4 org
773t Frontiers in Molecular Neuroscienced : Frontiers Media SAg 14q 14x 1662-5099
856u https://doi.org/10.3389/fnmol.2021.699562y Fulltext
856u https://www.frontiersin.org/articles/10.3389/fnmol.2021.699562/pdf
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-197224
8564 8u https://doi.org/10.3389/fnmol.2021.699562
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:147260202

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