Thank you for your interest! Here, I will introduce my research experiences.
This project was the focus of my master’s research, and I’m excited to share that our paper is currently under review.
Repairing severe injuries and soft tissue defects is challenging, with vascularization essential for tissue engineering success. Regenerative biomaterials
, especially natural ones, show promise by reducing immune response and promoting vascular integration, making them key for tissue restoration. For this work, I extracted an acellular extracellular matrix
from human adipose tissue, making it an ideal model for studying biomaterial vascularization due to its natural origin and lack of host cell interference.
Initially, I observed that the vasculature in our matrix derived from a host-generated collagen membrane formed on its surface [we name it Vascular Matrix Complex (VMC)
], which seemed at first consistent with the foreign-body capsule response often observed with implants. However, by employing vessel-tracing
techniques, I discovered that the true vascular source was the subcutaneous fascia rather than the surrounding tissue. Using in situ matrix-tracing
, cell-tracing
, Sirius red staining
, and collagen type analysis
, I uncovered a surprising finding: the collagen matrix wasn’t a result of a foreign-body reaction but rather a migrated layer of fascia that brought with it embedded blood vessels. Through repeated experiments—including fascia removal and blocking
—I confirmed that this migrating fascia was essential for the matrix’s vascularization.
The second part of this study explored the changes in vascular structures within the migrating fascia on the matrix surface. Using SEM
and whole-mount staining
, I observed a clear temporal pattern: blood vessels first developed on the matrix surface before penetrating into its core. Employing CurveAlign
and R
for fiber analysis, I found a correlation between this vascular growth pattern and the collagen architecture of the fascia, suggesting that fascia collagen might be directing vascularization.
Interestingly, the migrating fascia also exhibited spontaneous adipogenesis—a phenomenon I’m investigating further to understand whether it is induced by the adipose-derived matrix or other unknown factors. Going forward, I plan to continue exploring the role of fascia collagen in regulating blood vessel formation and its connection to this spontaneous adipogenesis.
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This project builds on our "Fascia-Mediated Biomaterial Vascularization" research. Our earlier findings revealed that the collagenous membrane, the VMC, surrounding implanted matrices resembles migrated fascia rather than a typical foreign body capsule.
Here, we compared histological properties between VMC and the fibrotic capsules of silicone implants, finding significant differences in thickness, collagen content, fiber density, and cellular infiltration. We also demonstrated the potential of Sodium Succinate to reduce fibrosis, offering promising insights for preventing post-implant contractures.
This experience was a truly formative one that ignited my passion for surgery. During my undergraduate years, I engaged in a two-year anatomy practicum at SMU, where I had the privilege of dissecting human specimens within China’s first established anatomy department. Over the two years, I meticulously dissected 18 facial muscle and vascular specimens and 45 foot ligament specimens, which were then displayed in our anatomy museum and utilized for systemic and regional anatomy courses for second-year students.
The experience also inspired my early research pursuits, leading me to initiate two projects. The first focused on the anatomy of the superior and inferior labial arteries
in relation to safe injection practices in facial aesthetics. This work mapped arterial distances from key landmarks on the lips to enhance guidance on avoiding danger zones in cosmetic injections. The second project, published in the Orthopaedic Journal of Sports Medicine, analyzed the anatomical variations in the ATFL and CFL ligaments of the ankle
to aid in reconstructive techniques after sprains, dissecting and measuring 66 foot ligament specimens to provide a foundation for ankle ligament reconstruction.
in Dissection Practice
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Lead researcher on a clinical and experimental study assessing correlations between BMI, Coleman fat density, stromal vascular fraction (SVF) cell count and viability, and ECM content to predict autologous fat graft retention.
Responsibilities included clinical sample collection
, laboratory processing, data measurement
, and establishing an animal fat graft model
. Histological assessments are ongoing, and the manuscript draft is in progress.
A clinical study assessing the effectiveness and safety of adipose collagen fragments (ACF)
in treating dark circles.
Responsibilities included ACF preparation
, extracellular vesicle extraction
from ACF, and histological characterization
of ACF properties. ↓↓↓
$Mesenchymal stem cells and their extracellular vesicles for autoimmune-related fibrotic skin diseases. ——— a review by Han Yang et al.$
This is my life.
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Dec 6, 2024, in Nanfang Hospital, Guangzhou