Sphingosine may have cytotoxic effects via apoptosis on the growth of keloid fibroblasts

被引:0
作者
Chang, SE
Kim, KJ
Ro, KH
Lim, YJ
Choi, JH
Moon, KC
Sung, K
机构
[1] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Dermatol, Seoul 138736, South Korea
[2] Seoul Natl Univ, Coll Med, Dept Anesthesiol, Seoul, South Korea
关键词
sphingosine; keloid; cytotoxic effect via apoptosis;
D O I
暂无
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Keloids are often resistant to treatment, causing much suffering to the patient. Our previous work found that ceramide (Cer) inhibits growth of fibroblasts via apoptosis. However, when compared to normal fibroblasts (NFs), which are quiescent, keloid fibroblasts (KFs) rapidly proliferate and are reported to be resistant to apoptosis via Cer. Sphingosine (Sph) is a metabolite product of ceramide that has some different biochemical properties. Thereofore, we investigated the cytotoxic effects of Sph on cultured fibroblasts from keloid lesions and normal skin in order to evaluate the possibility of using Sph in the treatment of keloid. We used the lactic dehydrogenase (LDH) method, MTT method, and propidium iodide (PI) method. Sph had cytotoxic effects via apoptosis on both the KFs and NFs. Our results indicate that Sph may be applicable to the future treatment of keloid.
引用
收藏
页码:1 / 5
页数:5
相关论文
共 25 条
  • [1] Ariga T, 1998, J LIPID RES, V39, P1
  • [2] Sphingomyelin metabolites in vascular cell signaling and atherogenesis
    Augé, N
    Nègre-Salvayre, A
    Salvayre, R
    Levade, T
    [J]. PROGRESS IN LIPID RESEARCH, 2000, 39 (03) : 207 - 229
  • [3] Sphingosine in apoptosis signaling
    Cuvillier, O
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2002, 1585 (2-3): : 153 - 162
  • [4] DBAIBO GS, 2000, J BIOL CHEM, V275, P15691
  • [5] A CONTROLLED TRIAL OF INTRALESIONAL RECOMBINANT INTERFERON-GAMMA IN THE TREATMENT OF KELOIDAL SCARRING - CLINICAL AND HISTOLOGIC-FINDINGS
    GRANSTEIN, RD
    ROOK, A
    FLOTTE, TJ
    HAAS, A
    GALLO, RL
    JAFFE, HS
    AMENTO, EP
    [J]. ARCHIVES OF DERMATOLOGY, 1990, 126 (10) : 1295 - 1302
  • [6] SPHINGOSINE INHIBITS PHORBOL ESTER-INDUCED INFLAMMATION, ORNITHINE DECARBOXYLASE ACTIVITY, AND ACTIVATION OF PROTEIN KINASE-C IN MOUSE SKIN
    GUPTA, AK
    FISHER, GJ
    ELDER, JT
    NICKOLOFF, BJ
    VOORHEES, JJ
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1988, 91 (05) : 486 - 491
  • [7] Keloid fibroblasts resist ceramide-induced apoptosis by overexpression of insulin-like growth factor I receptor
    Ishihara, H
    Yoshimoto, H
    Fujioka, M
    Murakami, R
    Hirano, A
    Fujii, T
    Ohtsuru, A
    Namba, H
    Yamashita, S
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2000, 115 (06) : 1065 - 1071
  • [8] Induction of apoptosis and potentiation of ceramide-mediated cytotoxicity by sphingoid bases in human myeloid leukemia cells
    Jarvis, WD
    Fornari, FA
    Traylor, RS
    Martin, HA
    Kramer, LB
    Erukulla, RK
    Bittman, R
    Grant, S
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (14) : 8275 - 8284
  • [9] Tumor necrosis factor alpha-induced apoptosis in cardiac myocytes - Involvement of the sphingolipid signaling cascade in cardiac cell death
    Krown, KA
    Page, MT
    Nguyen, C
    Zechner, D
    Gutierrez, V
    Comstock, KL
    Glembotski, CC
    Quintana, PJE
    Sabbadini, RA
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (12) : 2854 - 2865
  • [10] Involvement of sphingosine in dexamethasone-induced thymocyte apoptosis
    Lépine, S
    Lakatos, B
    Maziere, P
    Courageot, NP
    Sulpice, JC
    Giraud, F
    [J]. CELL SIGNALING, TRANSCRIPTION, AND TRANSLATION AS THERAPEUTIC TARGETS, 2002, 973 : 190 - 193