Microscopic image-based classification of adipocyte differentiation by machine learning

被引:1
|
作者
Noguchi, Yoshiyuki [1 ]
Murakami, Masataka [2 ]
Murata, Masayuki [3 ]
Kano, Fumi [4 ]
机构
[1] Univ Tokyo, Inst Adv Study, Int Res Ctr Neurointelligence, 7-3-1, Hongo, Bunkyo Ku, Tokyo 1138654, Japan
[2] Univ Tokyo, Grad Sch Arts & Sci, Dept Life Sci, 3-8-1 Komaba,Meguro Ku, Tokyo 1538902, Japan
[3] Tokyo Inst Technol, Multimodal Cell Anal Collaborat Res Cluster, 4259 Nagatsuta, Midori Ku, Yokohama, Kanagawa 2268503, Japan
[4] Tokyo Inst Technol, Inst Innovat Res, Cell Biol Ctr, 4259 Nagatsuta, Midori Ku, Yokohama, Kanagawa 2268503, Japan
关键词
Adipocyte differentiation; Obesity; Machine learning; Image analysis; PPAR-GAMMA; ADIPOGENIC DIFFERENTIATION; IN-VIVO; EXPRESSION; CELLS; GENE; GLUCOSE; FAT; MICE;
D O I
10.1007/s00418-022-02168-z
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Adipocyte differentiation is a sequential process involving increased expression of peroxisome proliferator-activated receptor gamma (PPAR gamma), adipocyte-specific gene expression, and accumulation of lipid droplets in the cytoplasm. Expression of the transcription factors involved is usually detected using canonical biochemical or biomolecular procedures such as Western blotting or qPCR of pooled cell lysates. While this provides a useful average index for adipogenesis for some populations, the precise stage of adipogenesis cannot be distinguished at the single-cell level, because the heterogenous nature of differentiation among cells limits the utility of averaged data. We have created a classifier to sort cells, and used it to determine the stage of adipocyte differentiation at the single-cell level. We used a machine learning method with microscopic images of cell stained for PPAR gamma and lipid droplets as input data. Our results show that the classifier can successfully determine the precise stage of differentiation. Stage classification and subsequent model fitting using the sequential reaction model revealed the action of pioglitazone and rosiglitazone to be promotion of transition from the stage of increased PPAR gamma expression to the next stage. This indicates that these drugs are PPAR gamma agonists, and that our classifier and model can accurately estimate drug action points and would be suitable for evaluating the stage/state of individual cells during differentiation or disease progression. The incorporation of both biochemical and morphological information derived from immunofluorescence image of cells and so overcomes limitations of current models.
引用
收藏
页码:313 / 327
页数:15
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