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干扰素γ对角质细胞与破骨细胞的影响 被引量:3

The Effect of IFN-γ to the Keratinocyte and Osteoclast
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摘要 干扰素γ(IFN-γ)是Th1细胞的标志性细胞因子,与机体多种疾病的发生有密切关系。IFN-γ可以通过促进角质细胞的增生并抑制其凋亡,刺激破骨细胞的形成,在银屑病、特异性皮炎等的上皮增生及类风湿性关节炎、骨质疏松等的骨质破坏过程中发挥重要作用。本文就IFN-γ对角质细胞与破骨细胞的影响及其在中耳胆脂瘤发病中的作用予以概述。 Interferon-γ (IFN-γ) is a label cytokine produced by Thl cell and related to various diseases. IFN-γ stimulates the proliferation, inhibit the apoptosis of horny cells, and improve the production of osteoclast, which plays important roles in psoriasis atopic dermatitis, arthritis, osteoporosis and so on. This article summarized the effects of IFN-γ in the keratinocyte and osteoclast,and its roles in the pathogenesy of in middle ear cholesteatoma.
出处 《医学综述》 2008年第20期3064-3067,共4页 Medical Recapitulate
关键词 干扰素Γ 角质细胞 破骨细胞 中耳胆脂瘤 Interferon-γ Keratinoeyte Osteoclast Middle ear cholesteatoma
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参考文献21

  • 1Gattoni A, Parlato A, Vangieri B, et al. Interferon-gamma: biologic functions and HCV therapy [ J ]. C lin Ter,2006,157 (4) :377-386.
  • 2Lew W, Bowcock AM, Krueger JG. Psoriasis vulgaris : cutaneous Lymphoid tissue supports T-cell activation and 'type 1 'inflammatory gene expression [ J ]. Trends Immunol,2004,25 ( 6 ) : 295-305.
  • 3Monica F, Maria L, Giusizieri N, et al. Impaired IFN-γ dependent inflammatory responses in human keratinocytes over expressing the suppressor of cytokine signalingl [ J ]. J Immunol, 2002,169 ( 3 ) : 434-442.
  • 4Winterfield S, Menter A, Gordon K, et al. Psoriasis treatment : current and emerging directed therapies [ J ]. Ann Rheum Dis, 2005, 64(2) :87-90.
  • 5Chen SH, Arany I, Apisarnthanarax N, et al. Response of keratinocytes from normal and psoriatic epidermis to interferon-gamma differs in the expression of zincalpha2-glycoprotein and cathepsin D [J]. FASEB J,2000,14(5) :565-571.
  • 6Tan N, Michalik L, Noy N, et al. Gritical roles of PPARβPδ in keratinocyte response to inflammation[ J]. Genes Dev,2001,15 (3) : 3263 -3277.
  • 7Gao Y, Grassi F, Ryan MR, et al. IFN-γ stimulates osteoclast formation and bone loss in vivo via antigen-driven T cellactivation [ J]. J Clin Invest ,2007,117 ( 1 ) : 122-132.
  • 8Takayanagi H, Sato K, Takaoka A, et al. Interplay between interferon and other cytokine systems in bone metabolism[ J]. Immunol Rev, 2005,208 (2) : 181-193.
  • 9Weitzmann MN, Pacifici R. Estrogen deficiency and bone. loss : an inflammatory tale [ J ]. J Clin Invest,2006,116 ( 4 ) : 1186-1194.
  • 10Cenci S,Toraldo G, Weitzmann MN, et al. Estrogen deficiency induces bone loss by increasing T cell proliferation and lifespan through IFN-gamma-induced class II transactivator. Proc [ J ]. Natl Acad Sci USA,2003,100 (8) : 10405-1 0410.

二级参考文献29

  • 1Schonermark M P, Issing P R, Erbrich B K,et al. Expression pattern of the plasminogen activator-plasmin system in human cholesteatoma. Ann Otol Rhinol Laryngol, 1999,108: 245- 252.
  • 2Shibosawa E,Tsutsumi K,Takakuwa T, et al. Stromal expression of matrix metalloprotease-9 in middle ear cholesteatomas. Am J Otol, 2000,21: 621- 624.
  • 3Schmidt M, Grunsfelder P, Hoppe F. Up-regulation of matrix metalloprotease-9 in middle ear cholesteatomacorrelations with growth factor expression in vivo? Eur Arch Otorhinolaryngol, 2001,258 : 472- 476.
  • 4Kleiner D E, Stetler-Stevenson W G. Quantitative zymography: detection of picogram quantities of gelatinases. Anal Biochem, 1994,218: 325 - 329.
  • 5Banerjee A R,Jones J L,Birchall J P,et al. Localization of matrix metalloproteinase-1 in cholesteatoma and deep meatal skin. Otol Neurotol, 2001,22 : 579- 581.
  • 6Lehman D A, Wilmoth J G, Prevatt A R, et al. Inhibition of matrix metalloproteinases in gerbil cholesteatoma:preliminary findings. Otolaryngol Head Neck Surg,2002,126: 404 - 408.
  • 7Sudhoff H,Bujia J,Borkowski G,et al. Basement membrane in middle ear cholesteatoma immunohistochemical and ultrastructural observations. Ann Otol Rhinol Laryngol, 1996,105:804-810.
  • 8Huang C C,Jeffrey M, Abramson M. Interleukin 1 causing bone destruction in middle ear cholesteatoma. Otolaryngol Head Neck Surg, 1987,98: 854- 859.
  • 9Tokuriki M, Noda I, Saito T, et al. Gene expression analysis of human middle ear cholesteatoma using complementary DNA arrays. Laryngoscope, 2003, 113: 808-814.
  • 10Sastry KV, Sharma SC, Mann SH. et al. Aural cholesteatoma: role of tumor necrosis factor-alpha in bone destruction. Am J Otol, 1999, 20: 158-161.

共引文献23

同被引文献25

  • 1任晓勇,陈文弦,崔鹏程,张全安.中耳胆脂瘤上皮中白介素-1α的表达[J].中国耳鼻咽喉头颈外科,2005,12(6):367-369. 被引量:5
  • 2胡向农,魏强.CpG ODN诱导浆细胞样树突状细胞免疫调节的作用机制[J].现代免疫学,2005,25(4):337-340. 被引量:3
  • 3陈晓飞,邓敏.Toll样受体病原识别及信号转导的研究新进展[J].中国感染控制杂志,2006,5(3):282-285. 被引量:2
  • 4Takahashi S,Nakano Y.Immunohistochemical demonstration of Langerhans' cell in cholesteatoma using an antiserum against S100 protein.Arch Otorhinolaryngol,1989,246(1):48-52.
  • 5Medzhitov R,Preston-Hurlburt P,Janeway CA.A human homologue of the Drosophila Toll protein signal saetivation of adaptive immunity.Nature,1997,388(6640):394-397.
  • 6Szczepanski M,Szyfter W,Jenek R,et al.Toll-like recptors 2,3 and 4 (TLR-2,TLR-3 and TLR-4) are expressed in the microenviranment of human acquired cholesteatoma.Eur Arch Otorhinolaryngol,2006,263 (7):603-607.
  • 7Bujia J,Kim C,Boyle D,et al.Quantitative analysis of interleukin-1-alpha gene expression in middle ear cholesteatoma.Laryngoscope,1996,106:217-220.
  • 8Liu Y, Krueger JG, Bowcockl AM. Psoriasis:genetic as- sociations and immune system changes Genes Immun, 2007,8( 1): 1 - 12.
  • 9Jain S, Kaur IR, Das S, Bhattacharya SN,and Singh A. T helper 1 to T helper 2 shift in cytokine expression an autoregulatory process in superantigenassociated psoriasis progression "Journal of Medical Microbiology,2009,58(2): 180-184.
  • 10Thangapazham RL, Sharma A, Maheshwari RK. Beneficial role of curcumin in skin diseases. Adv Exp Med Biol, 2007,595:343 -357.

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