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The effects of lysosomotropic amines on protein degradation, migration of nonhistone proteins to the nucleus, and cathepsin D in lymphocytes
Author(s) -
Polet Herman
Publication year - 1985
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.1041220312
Subject(s) - nucleus , microbiology and biotechnology , degradation (telecommunications) , chemistry , cathepsin , protein degradation , non histone protein , biochemistry , biology , enzyme , dna , computer science , telecommunications , histone
Various lysosomotropic amines have two parallel effects in human lymphocytes: they inhibit the degradation of cellular proteins and increase the migration of nonhistone proteins (NHP) from the cytoplasm to the nucleus. The increased nuclear level of NHP is associated with increased cellular binding of [ 3 H] actinomycin D, indicating an altered structure of chromatin. The agents inhibit the degradation of short‐and long‐lived proteins equally. Fractionation of the [ 3 H] NHP of the nucleus according to pH 2.5‐6.5 shows that [ 3 H] NHP with a high rate of degradation in untreated cells correspond to [ 3 H] NHP with a high rate of migration in cells treated with the agents. Eserine, amantadine, nicotine, atropine, benzylamine, and propranolol inhibit cathepsin D in concentrations causing proteolytic inhibition in cell cultures or in concentrations believed to be attained in lysosomes. The agents strongly inhibit the cellular accumulation of [ 3 H] chloroquine. The data support the proposal that the migration of NHP from the cytoplasm to the nucleus is the direct consequence of inhibited degradation of these proteins in lysosomes by the amines.