Sexual Autophagic Differences in the Androgen-Dependent Flank Organ of Syrian Hamsters

被引:15
作者
Coto-Montes, Ana [1 ]
Tomas-Zapico, Cristina [2 ]
Martinez-Fraga, Jorge [1 ]
Vega-Naredo, Ignacio [1 ]
Sierra, Veronica [1 ,3 ]
Caballero, Beatriz [1 ]
Huidobro-Fernandez, Covadonga [1 ]
Soria-Valles, Clara [1 ]
Tolivia, Delio [1 ]
Rodriguez-Colunga, Maria Josefa [1 ]
机构
[1] Univ Oviedo, Dept Morfol & Biol Celular, Fac Med, E-33006 Oviedo, Spain
[2] UAM, CSIC, Ctr Biol Mol Severo Ochoa, Madrid, Spain
[3] SERIDA, Villaviciosa, Spain
来源
JOURNAL OF ANDROLOGY | 2009年 / 30卷 / 02期
关键词
Beclin; 1; cathepsin D; LC3; PROGRAMMED CELL-DEATH; SEBACEOUS GLANDS; PROTEOLYTIC-ENZYMES; APOPTOSIS; PROTEIN; TESTOSTERONE; PATHWAY; GROWTH;
D O I
10.2164/jandrol.108.005355
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
The flank organ of the Syrian hamster shows a biodynamic response to androgenic stimulation and is, therefore, a suitable model for the study of androgenic effects on hair and sebaceous glands. This organ is susceptible to programmed cell death (PCD), a prominent feature associated with sexual organ adjustment. In the present report, the type of PCD (apoptosis or autophagy) exhibited by this organ was evaluated. Caspase-3 activity, indicative of apoptosis, was not detectable in flank organ homogenates. Furthermore, cytokeratins, which are normally degraded during apoptosis, remained intact. On the other hand, Western blotting of Beclin 1 and light chain 3-II, both important autophagy markers, revealed autophagic processes in the flank organ in both sexes, especially in females. Cathepsin D activity, higher in males than in females, and procathepsin D expression were also consistent with autophagy and not apoptosis. Taken together, these data indicate that macroautophagy, and not apoptosis, is the main mechanism by which the flank organ responds to androgen. This is the first direct evidence establishing the relationship between autophagy and morphological changes in androgen-dependent organs.
引用
收藏
页码:113 / 121
页数:9
相关论文
共 36 条
[21]   Protection against fatal Sindbis virus encephalitis by Beclin, a novel Bcl-2-interacting protein [J].
Liang, XH ;
Kleeman, LK ;
Jiang, HH ;
Gordon, G ;
Goldman, JE ;
Berry, G ;
Herman, B ;
Levine, B .
JOURNAL OF VIROLOGY, 1998, 72 (11) :8586-8596
[22]   Induction of autophagy and inhibition of tumorigenesis by beclin 1 [J].
Liang, XH ;
Jackson, S ;
Seaman, M ;
Brown, K ;
Kempkes, B ;
Hibshoosh, H ;
Levine, B .
NATURE, 1999, 402 (6762) :672-676
[23]  
Mezick JA, 1999, BRIT J DERMATOL, V140, P1100
[24]   PROTEOLYTIC-ENZYMES PAST AND PRESENT - THE 2ND GOLDEN ERA [J].
NEURATH, H .
PROTEIN SCIENCE, 1994, 3 (10) :1734-1739
[25]   PROTEOLYTIC PROCESSING AND REGULATION [J].
NEURATH, H .
ENZYME, 1991, 45 (5-6) :239-243
[26]   SEBACEOUS GLAND RESPONSE IN MAN TO ADMINISTRATION OF TESTOSTERONE DELTA4-ANDROSTENEDIONE AND DEHYDROISOANDROSTERONE [J].
POCHI, PE ;
STRAUSS, JS .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1969, 52 (01) :32-&
[27]   Microinjection of cathepsin D induces caspase-dependent apoptosis in fibroblasts [J].
Roberg, K ;
Kågedal, K ;
Öllinger, K .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 161 (01) :89-96
[28]   STEROID PATHWAYS IN SEBACEOUS GLANDS [J].
SANSONEBAZZANO, G ;
REISNER, RM .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1974, 62 (03) :211-216
[29]   ENDOGENOUS PROTEOLYTIC-ENZYMES IN CHICKEN MUSCLES - DIFFERENCES AMONG STRAINS WITH DIFFERENT GROWTH-RATES AND PROTEIN EFFICIENCIES [J].
SCHREURS, FJG ;
VANDERHEIDE, D ;
LEENSTRA, FR ;
DEWIT, W .
POULTRY SCIENCE, 1995, 74 (03) :523-537
[30]  
TAKAHASHI T, 1981, PROTEOLITIC ENZYME C, P567