Role of lysosomal cathepsins in naphthazarin- and Fas-induced apoptosis in oral squamous cell carcinoma cells

被引:10
|
作者
Johansson, AC [1 ]
Norberg-Spaak, L
Roberg, K
机构
[1] Linkoping Univ, Fac Hlth Sci, Div Pathol 2, S-58185 Linkoping, Sweden
[2] Linkoping Univ, Fac Hlth Sci, Div Otorhinolaryngol, S-58185 Linkoping, Sweden
关键词
caspases; cathepsin D; cell death; cysteine cathepsins; Fas death receptor; lysosomes; shedding; soluble Fas;
D O I
10.1080/00016480510043422
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Conclusion. Intracellular cysteine cathepsins are pro-apoptotic factors involved in activation of caspases in two oral squamous cell carcinoma (SCC) cell lines. Objective. To study the possible involvement of lysosomal cathepsins in oral SCC cell apoptosis. Material and methods. Apoptosis was induced in the two human oral SCC cell lines UT-SCC-20A and UT-SCC-24A using naphthazarin or anti-Fas antibodies, and was studied by analysis of caspase activity and nuclear morphology. Involvement of lysosomal cathepsins was investigated using the cysteine cathepsin inhibitor z-FA-FMK and the cathepsin D inhibitor pepstatin A. The amounts of cellular and soluble Fas death receptor were determined by ELISA. Results. Release of cathepsins from the lysosomes to the cytosol was observed early in apoptosis. Cysteine cathepsins were found to be involved in activation of caspases in response to treatment with naphthazarin or anti-Fas antibodies, but inhibition of cysteine cathepsin activity was not sufficient to prevent cell death. Moreover, inhibition of cysteine cathepsin activity resulted in increased expression of the Fas death receptor, suggesting involvement of extracellular cysteine cathepsins in death receptor shedding.
引用
收藏
页码:70 / 81
页数:12
相关论文
共 50 条
  • [31] Effects of PARP inhibition on drug and Fas-induced apoptosis in leukaemic cells
    Richardson, DS
    Allen, PD
    Kelsey, SM
    Newland, AC
    DRUG RESISTANCE IN LEUKEMIA AND LYMPHOMA III, 1999, 457 : 267 - 279
  • [32] Localization of Fas antigen in oral squamous cell carcinoma
    Muraki, Y
    Yoshioka, C
    Tateishi, A
    Fukuda, J
    Haneji, T
    Kobayashi, N
    BRITISH JOURNAL OF ORAL & MAXILLOFACIAL SURGERY, 1999, 37 (01): : 37 - 40
  • [33] Increase of Fas-induced apoptosis by inhibition of extracellular phosphorylation of Fas receptor in Jurkat cell line
    Lautrette, C.
    Loum-Ribot, E.
    Petit, D.
    Vermot-Desroches, C.
    Wijdenes, J.
    Jauberteau, M. O.
    APOPTOSIS, 2006, 11 (07) : 1195 - 1204
  • [34] Redox regulation of Fas-induced apoptosis and Fas ligand expression in human natural killer cells
    Furuke, K
    Bloom, ET
    FASEB JOURNAL, 1999, 13 (05): : A963 - A963
  • [35] Increase of Fas-induced apoptosis by inhibition of extracellular phosphorylation of Fas receptor in Jurkat cell line
    C. Lautrette*
    E. Loum-Ribot
    D. Petit
    C. Vermot-Desroches
    J. Wijdenes
    M. O. Jauberteau
    Apoptosis, 2006, 11 : 1195 - 1204
  • [36] Tumstatin induces apoptosis mediated by Fas signaling pathway in oral squamous cell carcinoma SCC-VII cells
    Hwang-Bo, Jeon
    Park, Jong-Hwa
    Chung, In Sik
    ONCOLOGY LETTERS, 2015, 10 (02) : 1016 - 1022
  • [37] Okadaic acid stimulates apoptosis through expression of Fas receptor and Fas ligand in human oral squamous carcinoma cells
    Goto, K
    Fukuda, J
    Haneji, T
    ORAL ONCOLOGY, 2002, 38 (01) : 16 - 22
  • [38] The mechanism of acacetin-induced apoptosis on oral squamous cell carcinoma
    Kim, Chae-Doo
    Cha, Jeong-Dan
    Li, Shenglin
    Cha, In-Ho
    ARCHIVES OF ORAL BIOLOGY, 2015, 60 (09) : 1283 - 1298
  • [39] Lack of a role for Jun kinase and AP-1 in Fas-induced apoptosis
    Lenczowski, JM
    Dominguez, L
    Eder, AM
    King, LB
    Zacharchuk, CM
    Ashwell, JD
    MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (01) : 170 - 181
  • [40] Susceptibility to FAS-induced apoptosis in human nontumoral enterocytes: Role of costimulatory factors
    Ruemmele, FM
    Russo, P
    Beaulieu, JF
    Dionne, S
    Levy, E
    Lentze, MJ
    Seidman, EG
    JOURNAL OF CELLULAR PHYSIOLOGY, 1999, 181 (01) : 45 - 54