A highly sensitive strategy for monitoring real-time proliferation of targeted cell types in vivo.
Hiroto SugawaraJunta ImaiJunpei YamamotoTomohito IzumiYohei KawanaAkira EndoMasato KohataJunro SeikeHaremaru KuboHiroshi KomamuraYuichiro MunakataYoichiro AsaiShinichiro HosakaShojiro SawadaShinjiro KodamaKei TakahashiKeizo KanekoHideki KatagiriPublished in: Nature communications (2023)
Cell proliferation processes play pivotal roles in timely adaptation to many biological situations. Herein, we establish a highly sensitive and simple strategy by which time-series showing the proliferation of a targeted cell type can be quantitatively monitored in vivo in the same individuals. We generate mice expressing a secreted type of luciferase only in cells producing Cre under the control of the Ki67 promoter. Crossing these with tissue-specific Cre-expressing mice allows us to monitor the proliferation time course of pancreatic β-cells, which are few in number and weakly proliferative, by measuring plasma luciferase activity. Physiological time courses, during obesity development, pregnancy and juvenile growth, as well as diurnal variation, of β-cell proliferation, are clearly detected. Moreover, this strategy can be utilized for highly sensitive ex vivo screening for proliferative factors for targeted cells. Thus, these technologies may contribute to advancements in broad areas of biological and medical research.
Keyphrases
- induced apoptosis
- cell proliferation
- signaling pathway
- cell cycle arrest
- high fat diet induced
- cancer therapy
- dna methylation
- healthcare
- insulin resistance
- metabolic syndrome
- gene expression
- single cell
- body mass index
- weight loss
- transcription factor
- fluorescent probe
- adipose tissue
- stem cells
- neoadjuvant chemotherapy
- skeletal muscle
- single molecule
- pregnancy outcomes
- cell therapy