|
|
Effects of PLGA Degradation on Angiogenesis in vitro |
WU Yan-ge, SUN Xue-feng, YANG Lin, WANG Zheng |
Shenzhen People's Hospital, the Second Clinical Medical College of Jinan University, Shenzhen 518020, China |
|
|
Abstract Objective: To investigate the influences of degradable PLGA scaffold on proliferation, migration and the formation of tube-like structure (TLS formation) of vascular endothelial cells.Methods: PLGA scaffold were immersed in PBS fluid to stimulate the degradation for 1, 2, and 4 weeks. HUVEC (Human Umbilical Vein Endothelial Cells) was cultured with degradation fluid. Cell proliferation, migration and TLS formation were detected by Brdu ELISA, Transwell chamber and tube formation.Results: The PLGA degradation fluid showed no effects on the migration, TLS formation of HUVEC, but the proliferation was increased in 1 week. With the prolonged degradation time, the migration and TLS formation were significantly decreased in 2 weeks, and the proliferation, migration and TLS formation were reduced remarkably in 4 weeks.Conclusions: At the beginning of degradation, PLGA could improve the proliferation function. The concentration of acid products increased with the increase of degradation time, and cell behaviors were retrained, thus inhibiting the angiogenesis of endothelial cells.
|
Received: 01 February 2012
Published: 25 July 2012
|
|
|
|
[1] Esmaeili F, Ghahremani M H, Esmaeili B, et al. PLGA nanoparticles of different surface properties: preparation and evaluation of their body distribution. International Journal of Pharmaceutics, 2008, 349(1-2): 249-255. [2] Chung T W, Wang S S, Tsai W J. Accelerating thrombolysis with chitosan-coated plasminogen activators encapsulated in poly (lactide-co-glycolide) (PLGA) nanoparticles. Biomaterials, 2008, 29(2): 228-237. [3] Macchiarini P, Jungebluth P, Go T, et al. Clinical transplantation of a tissue engineered airway. Lancet, 2008, 372(9655): 2023-2030. [4] Griffith L G, Naughton G. Tissue engineering-current challenges and expanding opportunities. Science, 2002, 295(8):1009-1014. [5] Cassell O C, Hofer S O, Morrison W A, et al. Vascularisation of tissue-engineered grafts: the regulation of angiogenesis in reconstructive surgery and in disease states. Br J Plast Surg, 2002, 55(8): 603-610. [6] Nomi M, Atala A, Coppi P D, et al. Principals of neovascularization for tissue engineering. Mol Aspects Med, 2002, 23(6): 463-483. [7] Bouhadir K H, Mooney D J. Promoting angiogenesis in engineered tissues. J Drug Target, 2001, 9(6): 397-406. [8] Pelissier P, Villars F, Mathoulin-Pelissier S, et al. Influences of vascularization and osteogenic cells on heterotopic bone formation within a madreporic ceramic in rats. Plast Reconstr Surg, 2003, 111(6): 1932-1941. [9] Elcin Y M, Dixit V, Gitnick G. Extensive in vivo angiogenesis following controlled release of human vascular endothelial cell growth factor: Implications for tissue engineering and wound healing. Artif Organs, 2001, 25(7): 558-565. [10] Peretes A, Baruch Y, Weisbuch F, et al. Enhancing the vascularization of three-dimensional porous alginate scaffolds by incorporation controlled release basic fibroblast growth factor microspheres. J Biomed Mater Res A, 2003, 65(4): 489-497. [11] Henno S, Lambotte J C, Glez D, et al. Characterization and quantification of angiogenesis in β-tricalcium phosphate implants by immunohistochemistry and transmission electron microscopy. Biomaterials, 2003, 24(19): 3173-3181. [12] 白峰, 王臻, 李爱民, 等. 两种不同三维结构β-TCP材料体内血管化的比较研究. 中国矫形外科杂志, 2007, 6(15): 451-454. Bai F, Wang Z, Li A M, et al. Comparative study on vascularization of two different three-dimensional structure β-TCP biomaterials in vivo. Orthopedic Journal of China, 2007, 6(15): 451-454. |
|
Viewed |
|
|
|
Full text
|
|
|
|
|
Abstract
|
|
|
|
|
Cited |
|
|
|
|
|
Shared |
|
|
|
|
|
Discussed |
|
|
|
|