<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mehta N</submitter><funding>National Science Foundation</funding><pagination>2103955</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8680429</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>31(43)</volume><pubmed_abstract>Stem cell-based therapies carry significant promise for treating human diseases. However, clinical translation of stem cell transplants for effective treatment requires precise non-destructive evaluation of the purity of stem cells with high sensitivity (&lt;0.001% of the number of cells). Here, a novel methodology using hyperspectral imaging (HSI) combined with spectral angle mapping-based machine learning analysis is reported to distinguish differentiating human adipose-derived stem cells (hASCs) from control stem cells. The spectral signature of adipogenesis generated by the HSI method enables identifying differentiated cells at single-cell resolution. The label-free HSI method is compared with the standard techniques such as Oil Red O staining, fluorescence microscopy, and qPCR that are routinely used to evaluate adipogenic differentiation of hASCs. HSI is successfully used to assess the abundance of adipocytes derived from transplanted cells in a transgenic mice model. Further, Raman microscopy and multiphoton-based metabolic imaging is performed to provide complementary information for the functional imaging of the hASCs. Finally, the HSI method is validated using matrix-assisted laser desorption/ionization-mass spectrometry imaging of the stem cells. The study presented here demonstrates that multimodal imaging methods enable label-free identification of stem cell differentiation with high spatial and chemical resolution.</pubmed_abstract><journal>Advanced functional materials</journal><pubmed_title>Multimodal Label-Free Monitoring of Adipogenic Stem Cell Differentiation Using Endogenous Optical Biomarkers.</pubmed_title><pmcid>PMC8680429</pmcid><funding_grant_id>2045640</funding_grant_id><pubmed_authors>Mehta N</pubmed_authors><pubmed_authors>Shaik S</pubmed_authors><pubmed_authors>Fu X</pubmed_authors><pubmed_authors>Sheikh E</pubmed_authors><pubmed_authors>Chaichi A</pubmed_authors><pubmed_authors>Gartia MR</pubmed_authors><pubmed_authors>Liu Q</pubmed_authors><pubmed_authors>Devireddy R</pubmed_authors><pubmed_authors>Donnarumma F</pubmed_authors><pubmed_authors>Hasan SMA</pubmed_authors><pubmed_authors>Prasad A</pubmed_authors><pubmed_authors>Sahu SP</pubmed_authors><pubmed_authors>Murray KK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multimodal Label-Free Monitoring of Adipogenic Stem Cell Differentiation Using Endogenous Optical Biomarkers.</name><description>Stem cell-based therapies carry significant promise for treating human diseases. However, clinical translation of stem cell transplants for effective treatment requires precise non-destructive evaluation of the purity of stem cells with high sensitivity (&lt;0.001% of the number of cells). Here, a novel methodology using hyperspectral imaging (HSI) combined with spectral angle mapping-based machine learning analysis is reported to distinguish differentiating human adipose-derived stem cells (hASCs) from control stem cells. The spectral signature of adipogenesis generated by the HSI method enables identifying differentiated cells at single-cell resolution. The label-free HSI method is compared with the standard techniques such as Oil Red O staining, fluorescence microscopy, and qPCR that are routinely used to evaluate adipogenic differentiation of hASCs. HSI is successfully used to assess the abundance of adipocytes derived from transplanted cells in a transgenic mice model. Further, Raman microscopy and multiphoton-based metabolic imaging is performed to provide complementary information for the functional imaging of the hASCs. Finally, the HSI method is validated using matrix-assisted laser desorption/ionization-mass spectrometry imaging of the stem cells. The study presented here demonstrates that multimodal imaging methods enable label-free identification of stem cell differentiation with high spatial and chemical resolution.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2025-04-04T07:26:38.733Z</modification><creation>2025-04-04T07:26:38.733Z</creation></dates><accession>S-EPMC8680429</accession><cross_references><pubmed>34924914</pubmed><doi>10.1002/adfm.202103955</doi></cross_references></HashMap>