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Old 11-07-2012, 09:37 AM   #1
Lani
Senior Member
 
Join Date: Mar 2006
Posts: 4,778
Thumbs up ?hope for effective treatment/cure for lymphedema

Therapeutic Lymphangiogenesis With Implantation of Adipose‐Derived Regenerative Cells

Yuuki Shimizu; Rei Shibata; Satoshi Shintani; Masakazu Ishii; Toyoaki Murohara
+ Author Affiliations

From the Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan
Correspondence to
: Toyoaki Murohara, MD, PhD, Department of Cardiology, Nagoya University Graduate School of Medicine, 65 Tsurumai, Showa‐ku, Nagoya, 466‐8550 Japan. E‐mail murohara@med.nagoya-u.ac.jp



Background Lymphedema is one of the serious clinical problems that can occur after surgical resection of malignant tumors such as breast cancer or intra‐pelvic cancers. However, no effective treatment options exist at present. Here, we report that implantation of adipose‐derived regenerative cells (ADRCs) can induce lymphangiogenesis in a mouse model of reparative lymphedema.

Methods and Results ADRCs were isolated from C57BL/6J mice. To examine the therapeutic efficacy of ADRC implantation in vivo, we established a new mouse model of tail lymphedema. Lymphedema was improved significantly by local injection of ADRCs (P<0.05). Histological analysis revealed that lymphatic capillary density was greater in the ADRC group than in the phosphate‐buffered saline control group (P<0.01). Tissue expression of vascular endothelial growth factor C mRNA and plasma levels of vascular endothelial growth factor C were greater in the ADRC group than in the control group (P<0.01 and P<0.05, respectively). ADRCs released vascular endothelial growth factor C, which directly stimulated lymphangiogenesis. Implantation of ADRCs also enhanced recruitment of bone marrow–derived M2 macrophages, which served as lymphatic endothelial progenitor cells.

Conclusions Implantation of autologous ADRCs could be a useful treatment option for patients with severe lymphedema via mediation of lymphangiogenesis. (J Am Heart Assoc. 2012;1:e000877 doi: 10.1161/JAHA.112.000877.)
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