Related Experiment Video
Updated: Jun 16, 2026

Characterization of Adipocyte-Derived Extracellular Vesicle Secretion Using a CD63-GFP Reporter Mouse Model In Vivo and In Vitro
Published on: December 5, 2025
Extracellular vesicles enriched with mitochondrial components from intermittently cold-exposed adipose tissue drive
Shaowei Zhu1,2,3, Jie Sun4, Chenggang Yi5
1The State Key Laboratory of Fluid Power and Mechatronic Systems, School of Mechanical Engineering, Zhejiang University, Hangzhou, 310027, China.
Abstract:
Current acellular adipose tissue engineering focuses primarily on structural regeneration, whereas functional metabolic recovery remains a major challenge. Extracellular vesicles (EV) derived from adipose tissue (AT-EV) have recently emerged as potent mediators of tissue regeneration, and cold stimulation has been reported to enhance the metabolic reprogramming of AT-EV. We have previously reported that fat grafts from cold-stimulated mice exhibited enhanced survival and adipose regeneration. Yet whether cold-induced AT-EV contribute to in vivo metabolic adipose regeneration remains unclear. Moreover, the cold stimulation temperatures used in traditional mouse models are often intolerable for humans. To address this, we developed a short-term intermittent mild cold exposure (STIMCE) protocol to metabolically activate murine adipose tissue for EV isolation (STIMCE-EV). Following only 3 or 7 days of STIMCE treatment, adipose tissue exhibited increased EV secretion and enrichment of mitochondrial components. Moreover, STIMCE-EV were efficiently incorporated into human acellular adipose matrix (AAM) hydrogel and exhibited controlled release in vitro. Injectable AAM@STIMCE-EV hydrogel transplantation in nude mice showed improved adipogenesis and volume retention in situ after 2 months. Importantly, the AAM@STIMCE-EV grafts improved cold adaptation and enhanced the thermogenic function of the host mice. Mechanistically, mmu-miR-296-3p was identified as a key regulatory factor within STIMCE-EV. Exogenous mmu-miR-296-3p supplementation significantly improved the adipogenic regeneration of AAM. Overall, this study presents a metabolically activated, cell-free adipose regeneration strategy that combines STIMCE-EV with AAM scaffolds. This minimally invasive and injectable system enables functional adipose tissue regeneration with systemic thermogenic metabolic activity, providing a promising translational solution for soft tissue reconstruction.
