目的探討p38蛋白激酶(p38 MAPK)在小腸移植早期排斥反應(yīng)中腸黏膜上皮細(xì)胞凋亡機(jī)理中的作用。
方法選用近交系SD和Wistar大鼠進(jìn)行節(jié)段性小腸移植,實(shí)驗(yàn)分3組: 同基因移植組(Wistar→Wistar組)、異基因移植組(SD→Wistar組)和異基因移植加環(huán)孢素A組(SD→Wistar+CsA組)。分別于移植術(shù)后1、3、5及7 d采集移植腸管行病理學(xué)檢查排斥反應(yīng),TUNEL法檢測(cè)凋亡細(xì)胞,并行Westernblotting測(cè)定p38 MAPK表達(dá); 同時(shí),ELISA法測(cè)定血清TNFα活性。
結(jié)果SD→Wistar組腸黏膜上皮細(xì)胞發(fā)生輕、中、重度排斥反應(yīng)中存在細(xì)胞凋亡,凋亡細(xì)胞數(shù)隨排斥反應(yīng)的加重而增加(P<0.01); Wistar→Wistar組排斥反應(yīng)輕微,凋亡細(xì)胞數(shù)無明顯變化(P gt;0.05); SD→Wistar+CsA組隨著CsA的應(yīng)用,排斥反應(yīng)逐漸得到控制,且凋亡細(xì)胞數(shù)也隨著減少。SD→Wistar組及SD→Wistar+CsA組的血清TNFα隨移植腸管上皮細(xì)胞凋亡的輕重而發(fā)生相應(yīng)的變化(P<0.01)。p38 MAPK在SD→Wistar組隨凋亡細(xì)胞數(shù)增加而表達(dá)加強(qiáng)(P<0.01),Wistar→Wistar組p38 MAPK表達(dá)無明顯變化(P gt;0.05),在SD→Wistar+CsA組隨凋亡細(xì)胞數(shù)而發(fā)生相應(yīng)的變化(P<0.01)。小腸移植早期排斥反應(yīng)中腸黏膜上皮細(xì)胞凋亡現(xiàn)象與p38 MAPK呈正相關(guān)(r=0.875,P<0.01),血清TNFα與移植腸上皮細(xì)胞凋亡呈正相關(guān)(r=0.837, P<0.01),血清TNFα與p38 MAPK亦呈正相關(guān)(r=0.826,P<0.01)。
結(jié)論大鼠小腸移植排斥反應(yīng)中存在腸黏膜上皮細(xì)胞凋亡現(xiàn)象,p38 MAPK參與細(xì)胞凋亡信號(hào)轉(zhuǎn)導(dǎo)過程并起重要作用。
引用本文: 張健,胡祥. p38蛋白激酶在小腸移植后腸黏膜上皮細(xì)胞凋亡機(jī)理中的作用. 中國(guó)普外基礎(chǔ)與臨床雜志, 2006, 13(1): 66-70. doi: 復(fù)制
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2. | Krams SM, Hayashi M, Fox CK, et al. CD8+ cells are not necessary for allograft rejection or the induction of apoptosis in an experimental model of small intestinal transplantation [J]. J Immunol, 1998; 160(8)∶3673. |
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9. | Raff MC, Barres BA, Burne JF, et al. Programmed cell death and the control of cell survival: lessons from the nervous system [J]. Science, 1993; 262(5134)∶695. |
10. | Cerwenka A, Kovar H, Majdic O, et al. Fas and activationinduced apoptosis are reduced in human T cells preactivated in the presence of TGFbeta 1 [J]. J Immunol, 1996; 156(2)∶459. |
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12. | Han J, Lee JD, Bibbs L, et al. A MAP kinase targeted by endotoxin and hyperosmolarity in mammalian cells [J]. Science, 1994; 265(5173)∶808. |
13. | 姜勇, 劉愛華, 張琳, 等. 脂多糖激活p38在誘導(dǎo)腫瘤壞死因子α基因表達(dá)中的作用 [J]. 中華醫(yī)學(xué)雜志, 1999; 79(5)∶360. |
- 1. Lee RG, Tsamandas AC, AbuElmagd K, et al. Histologic spectrum of acute cellular rejection in human intestinal allografts [J]. Transplant Proc, 1996; 28(5)∶ 2767.
- 2. Krams SM, Hayashi M, Fox CK, et al. CD8+ cells are not necessary for allograft rejection or the induction of apoptosis in an experimental model of small intestinal transplantation [J]. J Immunol, 1998; 160(8)∶3673.
- 3. Schmid T, Oberhuber G, Korozsi G, et al. Histologic pattern of small bowel allograft rejection in the rat. Mucosal biopsies do not provide sufficient information [J]. Gastroenterology, 1989; 96(6)∶1529.
- 4. Rosemurgy AS, Schraut WH. Small bowel allografts. Sequence of histologic changes in acute and chronic rejection [J]. Am J Surg, 1986; 151(4)∶470.
- 5. Lomo J, Blomhoff HK, Beiske K, et al. TGFbeta 1 and cyclic AMP promote apoptosis in resting human B lymphocytes [J]. J Immunol, 1995; 154(4)∶1634.
- 6. Smyth MJ, Trapani JA. Granzymes: exogenous proteinases that induce target cell apoptosis [J]. Immunol Today, 1995; 16(4)∶202.
- 7. Kerr JF, Winterford CM, Harmon BV. Apoptosis. Its significance in cancer and therapy [J]. Cancer, 1994; 73(8)∶2013.
- 8. Ogawa N, Dang H, Talal N. Apoptosis and autoimmunity [J]. J Autoimmun, 1995; 8(1)∶1.
- 9. Raff MC, Barres BA, Burne JF, et al. Programmed cell death and the control of cell survival: lessons from the nervous system [J]. Science, 1993; 262(5134)∶695.
- 10. Cerwenka A, Kovar H, Majdic O, et al. Fas and activationinduced apoptosis are reduced in human T cells preactivated in the presence of TGFbeta 1 [J]. J Immunol, 1996; 156(2)∶459.
- 11. Wei S, Liu JH, EplingBurnette PK, et al. Critical role of Lyn kinase in inhibition of neutrophil apoptosis by granulocytemacrophage colonystimulating factor [J]. J Immunol, 1996; 157(11)∶5155.
- 12. Han J, Lee JD, Bibbs L, et al. A MAP kinase targeted by endotoxin and hyperosmolarity in mammalian cells [J]. Science, 1994; 265(5173)∶808.
- 13. 姜勇, 劉愛華, 張琳, 等. 脂多糖激活p38在誘導(dǎo)腫瘤壞死因子α基因表達(dá)中的作用 [J]. 中華醫(yī)學(xué)雜志, 1999; 79(5)∶360.