【摘 要】 目的 音猬因子(Sonic hedgehog,Shh)介導(dǎo)的信號(hào)參與調(diào)控血管生成的重要環(huán)節(jié)。研究不同濃度的重組Shh-N(recombinant Shh N-termitant,rShh-N)對(duì)BMSCs表達(dá)和分泌VEGF和bFGF的影響。 方法 取健康3日齡SD大鼠骨髓分離培養(yǎng)BMSCs,體外擴(kuò)增至第3代,分別用含0、10、100、200 ng/mL rShh-N的L-DMEM培養(yǎng)BMSCs,作為A、B、C、D組。培養(yǎng)12、24、48、72 h后行ELISA法檢測(cè)各組上清液中VEGF和bFGF的濃度,實(shí)時(shí)熒光定量PCR法檢測(cè)各組VEGF和bFGF mRNA的表達(dá)水平。 結(jié)果 在基因表達(dá)水平上,D組各時(shí)間點(diǎn)的VEGF和bFGF mRNA表達(dá)量均明顯高于A組(P lt; 0.05),且在12、48 h表達(dá)量高于24、72 h(P lt; 0.01);C組在各時(shí)間點(diǎn)均促進(jìn)bFGF mRNA表達(dá)(P lt; 0.05),在24~72 h促進(jìn)VEGF mRNA表達(dá)(P lt; 0.05),且在72 h時(shí)表達(dá)量均最高(P lt; 0.01);B組在12 h抑制VEGF mRNA表達(dá)(P lt; 0.05),48 h和72 h表現(xiàn)出促進(jìn)作用(P lt; 0.05),在12~48 h明顯促進(jìn)bFGF mRNA表達(dá)(P lt; 0.05),且在48 h時(shí)的表達(dá)量最高(P lt; 0.01)。在蛋白水平上,D組各時(shí)間點(diǎn)VEGF和bFGF分泌量均高于A組(P lt; 0.01);C組在24~72 h VEGF和bFGF分泌量明顯多于A組(P lt; 0.05);B組在12 h和48 h抑制VEGF的分泌(P lt; 0.05),24 h增加其分泌作用(P lt; 0.05),而在24 h和48 h促進(jìn)bFGF的分泌(P lt; 0.05)。各組在48 h和72 h時(shí)的VEGF和bFGF分泌量明顯多于12 h和24 h(P lt; 0.05)。 結(jié)論 rShh-N可促進(jìn)BMSCs表達(dá)和分泌VEGF和bFGF,為進(jìn)一步探討rShh-N和MSCs聯(lián)合應(yīng)用于治療缺血性相關(guān)疾病以及促進(jìn)骨修復(fù)重建的可行性提供了實(shí)驗(yàn)依據(jù)。
引用本文: 蔡加琴 ,黃益洲,陳曉禾,謝紅蕾,黃永燦,鄧力. 音猬因子調(diào)控BMSCs表達(dá)和分泌VEGF及bFGF的實(shí)驗(yàn)研究. 中國修復(fù)重建外科雜志, 2012, 26(1): 112-116. doi: 復(fù)制
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1. | Med, 2007, 17(3): 77-83. |
2. | signaling. Nat Med, 2005, 11(11): 1197-1204. |
3. | of bone marrow stromal cells after cerebral ischemia in rats. Stroke, 2001, 32(4): 1005-1011. |
4. | hedgehog pathway in response to skeletal muscle ischemia. Circulation, 2003, 108(4): 479-485. |
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8. | stem cells improves cardiac function in rats with acute myocardial. |
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16. | Kusano KF, Pola R, Murayama T, et al. Sonic hedgehog myocardial gene therapy: tissue repair through transient reconstitution of embryonic. |
17. | Lavine KJ, Kovacs A, Ornitz DM. Hedgehog signaling is critical for maintenance of the adult coronary vasculature in mice. J Clin Invest, 2008, 118(7): 2404-2414. |
18. | 蔡加琴, 鄧力. Hedgehog信號(hào)通路對(duì)MSCs的調(diào)控. 中國修復(fù)重建外科雜志, 2010, 24(8): 993-996. |
19. | Donahue JK. Gene therapy, angiogenesis, Sonic Hedgehog: Sonic the Hedgehog to the rescue? Gene Ther, 2006, 13(13): 998-999. |
20. | Chen J, Li Y, Wang L, et al. Therapeutic benefit of intravenous administration. |
21. | Tang J, Xie Q, Pan G, et al. Mesenchymal stem cells participate in angiogenesis and improve heart function in rat model of myocardial ischemia with reperfusion. Eur J Cardiothorac Surg, 2006, 30(2): 353-361. |
22. | Al-Khaldi A, Al-Sabti H, Galipeau J, et al. Therapeutic angiogenesis using autologous bone marrow stromal cells: improved blood flow in a chronic limb ischemia model. Ann Thorac Surg, 2003, 75(1): 204-209. |
23. | Zhou Y, Guan XX, Zhu ZL, et al. Caffeine inhibits the viability and osteogenic differentiation of rat bone marrow-derived mesenchymal stromal cells. Br J Pharmacol, 2010, 161(7): 1542-1552. |
24. | 金惠銘, 李先濤. 血管新生的調(diào)控. 中國微循環(huán), 2001, 5(2): 85-88. |
25. | Pola R, Ling L, Aprahamian TR, et al. Postnatal recapitulation of embryonic. |
26. | Kusano KF, Allendoerfer KL, Munger W, et al. Sonic hedgehog induces arteriogenesis in diabetic vasa nervorum and restores function in diabetic. |
27. | Asai J, Takenaka H, Kusano KF, et al. Topical sonic hedgehog gene therapy accelerates wound healing in diabetes by enhancing endothelial. |
28. | Warzecha J, Göttig S, Brüning C, et al. Sonic hedgehog protein promotes. |
29. | Nagaya N, Fujii T, Iwase T, et al. Intravenous administration of mesenchymal. |
30. | Jemtland R, Divieti P, Lee K, et al. Hedgehog promotes primary osteoblast. |
31. | Yuasa T, Kataoka H, Kinto N, et al. Sonic hedgehog is involved in osteoblast differentiation by cooperating with BMP-2. J Cell Physiol, 2002, 193(2): 225-232. |
32. | Dohle E, Fuchs S, Marlen K, et al. Sonic hedgehog promotes angiogenesis. |
33. | Suzuki T, Miyamoto T, Fujita N, et al. Osteoblast-specific An gio poi etin1 overexpression increases bone mass. Biochem Biophys Res Commun, 2007, 362(4): 1019-1025. |
- 1. Med, 2007, 17(3): 77-83.
- 2. signaling. Nat Med, 2005, 11(11): 1197-1204.
- 3. of bone marrow stromal cells after cerebral ischemia in rats. Stroke, 2001, 32(4): 1005-1011.
- 4. hedgehog pathway in response to skeletal muscle ischemia. Circulation, 2003, 108(4): 479-485.
- 5. neuropathy. Arterioscler Thromb Vasc Biol, 2004, 24(11): 2102-2107.
- 6. progenitor cell-mediated microvascular remodeling. Circulation, 2006, 113(20): 2413-2424.
- 7. proliferation and chondrogenic differentiation of bone marrow-derived mesenchymal stem cells in vitro. J Orthop Sci, 2006, 11(5): 491-496.
- 8. stem cells improves cardiac function in rats with acute myocardial.
- 9. infarction through angiogenesis and myogenesis. Am J Physiol Heart Circ Physiol, 2004, 287(6): 2670-2676.
- 10. differentiation and increases pthrp mRNA expression and ipthrp secretion. Bone, 2003, 32(6): 611-620.
- 11. and osteogenesis in a coculture system consisting of primary osteoblasts and outgrowth endothelial cells. Tissue Eng Part A, 2010, 16(4): 1235-1246.
- 12. Cohen MM Jr. The hedgehog signaling network. Am J Med Genet A, 2003, 123A(1): 5-28.
- 13. Pola R, Ling L, Silver M, et al. The morphogen sonic hedgehog is an indirect angiogenic agent upregulating two families of angiogenic growth factors. Nat Med, 2001, 7(6): 706-711.
- 14. Byrd N, Grabel L. Hedgehog signaling in murine vasculogenesis and angiogenesis. Trends Cardiovasc Med, 2004, 14(8): 308-313.
- 15. Lavine KJ, Ornitz DM. Rebuilding the coronary vasculature: hedgehog as a new candidate for pharmacologic revascularization. Trends Cardiovasc.
- 16. Kusano KF, Pola R, Murayama T, et al. Sonic hedgehog myocardial gene therapy: tissue repair through transient reconstitution of embryonic.
- 17. Lavine KJ, Kovacs A, Ornitz DM. Hedgehog signaling is critical for maintenance of the adult coronary vasculature in mice. J Clin Invest, 2008, 118(7): 2404-2414.
- 18. 蔡加琴, 鄧力. Hedgehog信號(hào)通路對(duì)MSCs的調(diào)控. 中國修復(fù)重建外科雜志, 2010, 24(8): 993-996.
- 19. Donahue JK. Gene therapy, angiogenesis, Sonic Hedgehog: Sonic the Hedgehog to the rescue? Gene Ther, 2006, 13(13): 998-999.
- 20. Chen J, Li Y, Wang L, et al. Therapeutic benefit of intravenous administration.
- 21. Tang J, Xie Q, Pan G, et al. Mesenchymal stem cells participate in angiogenesis and improve heart function in rat model of myocardial ischemia with reperfusion. Eur J Cardiothorac Surg, 2006, 30(2): 353-361.
- 22. Al-Khaldi A, Al-Sabti H, Galipeau J, et al. Therapeutic angiogenesis using autologous bone marrow stromal cells: improved blood flow in a chronic limb ischemia model. Ann Thorac Surg, 2003, 75(1): 204-209.
- 23. Zhou Y, Guan XX, Zhu ZL, et al. Caffeine inhibits the viability and osteogenic differentiation of rat bone marrow-derived mesenchymal stromal cells. Br J Pharmacol, 2010, 161(7): 1542-1552.
- 24. 金惠銘, 李先濤. 血管新生的調(diào)控. 中國微循環(huán), 2001, 5(2): 85-88.
- 25. Pola R, Ling L, Aprahamian TR, et al. Postnatal recapitulation of embryonic.
- 26. Kusano KF, Allendoerfer KL, Munger W, et al. Sonic hedgehog induces arteriogenesis in diabetic vasa nervorum and restores function in diabetic.
- 27. Asai J, Takenaka H, Kusano KF, et al. Topical sonic hedgehog gene therapy accelerates wound healing in diabetes by enhancing endothelial.
- 28. Warzecha J, Göttig S, Brüning C, et al. Sonic hedgehog protein promotes.
- 29. Nagaya N, Fujii T, Iwase T, et al. Intravenous administration of mesenchymal.
- 30. Jemtland R, Divieti P, Lee K, et al. Hedgehog promotes primary osteoblast.
- 31. Yuasa T, Kataoka H, Kinto N, et al. Sonic hedgehog is involved in osteoblast differentiation by cooperating with BMP-2. J Cell Physiol, 2002, 193(2): 225-232.
- 32. Dohle E, Fuchs S, Marlen K, et al. Sonic hedgehog promotes angiogenesis.
- 33. Suzuki T, Miyamoto T, Fujita N, et al. Osteoblast-specific An gio poi etin1 overexpression increases bone mass. Biochem Biophys Res Commun, 2007, 362(4): 1019-1025.