Distribution of catalase and its modulation by 12-O-tetradecanoylphorbol-13-acetate in murine dermis and subpopulations of keratinocytes differing in their stages of differentiation.
Distribution of catalase and its modulation by 12-O-tetradecanoylphorbol-13-acetate in murine dermis and subpopulations of keratinocytes differing in their stages of differentiation.
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过氧化氢酶的分布及其在小鼠真皮和不同分化阶段的角质形成细胞亚群中 12-O-十四烷酰佛波醇-13-乙酸酯的调节。
DOI:
10.1093/carcin/9.7.1259
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发表时间:
1988
期刊:
影响因子:
4.7
通讯作者:
Cantu,AR
中科院分区:
文献类型:
--
作者:
ReinersJr,JJ;Hale,MA;Cantu,AR
Topical treatment of female SENCAR mice with 12-O-tetradecanoylphorbol- 13-acetate (TPA) reduced both dermal and epidermal catalase-specific activities 38% and 51% within 6 h and 18 h of promoter application, respectively. Dermal catalase activity recovered to control levels within 72 h of treatment whereas epidermal catalase activity remained suppressed. Activity measurements were also made in four subpopulations of keratinocytes prepared by Percoll gradient centrifugation that differed in their stages of differentiation. Catalase-specific activity increased with keratinocyte maturity and ranged from 45–54 U /mg protein for basal cell preparations to 252 U /mg protein for granular-squamous cell preparations. Pretreatment of the epidermis for 16 –18 h with TPA (2 μg) uniformly reduced catalase-specific activity 46 –52 % in all keratinocyte subpopulations prepared by Percoll gradient centrifugation. Similarly, plots of catalase units per cell versus extracted protein per cell suggested 55 –60 % decreases in catalase activity in basal and spinous cell keratinocytes of TPA treated epidermis. Furthermore, catalase-specific activity in homogenates of whole epidermis (144 –182 units /mg protein) was most similar to the activity of the granular/squamous keratinocyte subpopulation. Collectively, these studies suggest that: (i) TPA reduces the capacity for H2O2detoxification by catalase throughout the epidermis; and (ii) activity measurements on unfractionated epidermal preparations may not be representative of the basal cell keratinocyte population.
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DOI:
10.1016/0005-2760(85)90023-2
发表时间:
1985-06
期刊:
Biochimica et biophysica acta
影响因子:
--
作者:
J. Turk;B. Wolf;P. Comens;J. Colca;B. Jakschik;M. Mcdaniel
通讯作者:
J. Turk;B. Wolf;P. Comens;J. Colca;B. Jakschik;M. Mcdaniel
DOI:
10.1016/0005-2760(87)90119-6
发表时间:
1987
期刊:
Biochimica et biophysica acta
影响因子:
--
作者:
J. Evans;Y. Leblanc;B. Fitzsimmons;S. Charleson;D. Nathaniel;C. Léveillé
通讯作者:
C. Léveillé
影响因子:
6.1
作者:
J. Nakao;Y. Koshihara;H. Ito;S. Murota;W. Chang
通讯作者:
W. Chang
DOI:
--
发表时间:
1984
期刊:
Prostaglandins Leukotrienes and Medicine
影响因子:
--
作者:
Hassan Salari;Pierre Braquet;P. Borgeat
通讯作者:
P. Borgeat
影响因子:
2.9
作者:
Boeynaems,JM;Brash,AR;Oates,JA;Hubbard,WC
通讯作者:
Hubbard,WC