PEČINKA, Lukáš, Lukáš MORÁŇ, Jarmila HERŮDKOVÁ, Katarína ČIMBOROVÁ, Türkan PORTAKAL, Petra KOVAČOVICOVÁ, Vendula PELKOVÁ, Hana KOTASOVÁ, Josef HAVEL, Aleš HAMPL a Petr VAŇHARA. Mass spectrometry for monitoring and quality control of differentiation of pluripotent stem cells to lung progenitors using biostatistical models. In 8th Lipidomics Forum. 2023.
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Základní údaje
Originální název Mass spectrometry for monitoring and quality control of differentiation of pluripotent stem cells to lung progenitors using biostatistical models
Autoři PEČINKA, Lukáš (203 Česká republika, domácí), Lukáš MORÁŇ (203 Česká republika, domácí), Jarmila HERŮDKOVÁ (703 Slovensko, domácí), Katarína ČIMBOROVÁ (703 Slovensko, domácí), Türkan PORTAKAL (792 Turecko, domácí), Petra KOVAČOVICOVÁ (703 Slovensko, domácí), Vendula PELKOVÁ (203 Česká republika, domácí), Hana KOTASOVÁ (203 Česká republika, domácí), Josef HAVEL (203 Česká republika, domácí), Aleš HAMPL (203 Česká republika, domácí) a Petr VAŇHARA (203 Česká republika, garant, domácí).
Vydání 8th Lipidomics Forum, 2023.
Další údaje
Originální jazyk angličtina
Typ výsledku Konferenční abstrakt
Obor 30402 Technologies involving the manipulation of cells, tissues, organs or the whole organism
Stát vydavatele Rakousko
Utajení není předmětem státního či obchodního tajemství
WWW URL
Kód RIV RIV/00216224:14310/23:00134279
Organizační jednotka Přírodovědecká fakulta
Klíčová slova anglicky Lung progenitors; tissue engineering; MALDI TOF MS;quality control; stem cells
Změnil Změnil: doc. RNDr. Petr Vaňhara, Ph.D., učo 43385. Změněno: 24. 11. 2023 07:28.
Anotace
With increasing demands on precise analyses of biological samples in complex biological matrices, there is also need to develop and optimize mass spectrometric (MS) methods. The whole cell MALDI TOF MS is already used in clinical microbiology and diagnostics. In recent years it has been introduced also to cell biology, immunology, and cancer biology. Recently we used the whole cell-MS to monitor cultures of stem cells and progenitors and elucidate phenotypic shifts in long-term cultures. Here we demonstrated precise tracking of differentiation trajectory of human embryonic stem cells (hESCs) to lung epithelial progenitors by whole cell MS coupled with biostatistical modelling. Human embryonic stem cells (hESCs) possess unlimited differentiation potential and capacity to self-renew indefinitely. The hESC-derived, expandable lung epithelia (ELEP) used in this study were recently established in our lab to address histogenesis and regeneration of functional lung cell types. Differentiation of hESCs towards ELEPs is a complex process that shows substantial heterogeneity and can also produce aberrant cells with unwanted properties, such as lack of functional phenotype, or propensity to cancer growth. The differentiation process can be outlined specifically by molecular markers, but an unbiased, sensitive, and robust tool for the discrimination of ELEPs from pluripotent or transitional stages is still missing. In this work, we optimized the whole cell MS for lipid analysis, and coupled it with the multivariate statistical methods and supervised methods based on machine learning to follow differentiation of hESCs to ELEPs. We visualized the full differentiation trajectory based on spectral data only and revealed also some phenotypic abnormalities linked to passage number, and by proxy aneuploidy status of hESCs. Various extraction methods were tested to monitor changes in cellular lipids during the differentiation process. Finally, Folch´s method using chloroform/methanol/water has been selected and followed through this work. Sinapinic acid and 9-Aminoacridine matrix were used for MS measurement. MS measurements were combined with in-house developed R scripts. Data obtained from mass spectra were analyzed via several methods including principal component analysis (PCA), heatmap, and boxplots. Data were also analyzed by supervised methods (decision tree, random forest, and artificial neural networks). Mass spectra at various differentiation stages revealed different spectral fingerprints which allowed for successful classification in mathematical space using PCA and others. In summary, whole cell-MS is a promising tool for complex cultures of hESC-derived lung cells and progenitors, with potential clinical translation. Supported by the Grant Agency of Czech Republic (GA23-06675S) and by Masaryk University (MUNI/A/1298/2022, MUNI/A/1301/2022, and MUNI/11/ACC/3/2022).
Návaznosti
GA23-06675S, projekt VaVNázev: Plicní stres a regenerace
Investor: Grantová agentura ČR, Plicní stres a regenerace
MUNI/A/1298/2022, interní kód MUNázev: Základní a aplikovaný výzkum a vývoj metod chemické a fyzikálně chemické analýzy pro studium přírody a pokročilé technologie
Investor: Masarykova univerzita, Základní a aplikovaný výzkum a vývoj metod chemické a fyzikálně chemické analýzy pro studium přírody a pokročilé technologie
MUNI/A/1301/2022, interní kód MUNázev: Zdroje pro tkáňové inženýrství 13
Investor: Masarykova univerzita, Zdroje pro tkáňové inženýrství 13
MUNI/11/ACC/3/2022, interní kód MUNázev: Bioanalytical quality control of cGMP/ATMP-grade stem cells and progenitors
Investor: Masarykova univerzita, Bioanalytical quality control of cGMP/ATMP-grade stem cells and progenitors, Accelerate
VytisknoutZobrazeno: 18. 7. 2024 09:38