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Isolation and Culture of Primary Mouse Keratinocytes from Neonatal and Adult Mouse Skin
Published on: July 14, 2017
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MiR-378b Promotes Differentiation of Keratinocytes through NKX3.1
Xi-Liang Wang1, Tao Zhang1, Jing Wang2
1Key Laboratory of Cell Biology, Ministry of Public Health of China, Department of Stem Cells and Regenerative Medicine, China Medical University, Shenyang, 110122, China.
Plos One
|August 28, 2015
Summary
MicroRNA-378b (miR-378b) promotes keratinocyte differentiation by targeting NKX3.1. This finding offers a potential new strategy for skin injury and repair treatments.
Area of Science:
- Molecular Biology
- Cell Biology
- Dermatology
Background:
- MicroRNAs (miRNAs) are key regulators in cellular processes, including keratinocyte differentiation.
- Understanding miRNA roles is crucial for skin biology and therapeutic development.
Purpose of the Study:
- To investigate the role of miR-378b in keratinocyte differentiation.
- To identify the molecular targets of miR-378b in this process.
Main Methods:
- Microarray assay to measure miRNA expression during keratinocyte differentiation.
- Functional assays to assess the effects of miR-378b on keratinocyte proliferation, migration, and differentiation.
- Luciferase reporter assays to confirm direct targeting of NKX3.1 by miR-378b.
Main Results:
- miR-378b expression significantly increased during keratinocyte differentiation.
- miR-378b inhibited keratinocyte proliferation, migration, and differentiation.
- miR-378b was confirmed to directly target NKX3.1.
- Silencing NKX3.1 mimicked the effects of miR-378b overexpression.
Conclusions:
- miR-378b promotes keratinocyte differentiation by targeting NKX3.1.
- Modulating miR-378b presents a potential therapeutic strategy for skin injury and repair.

