Biosyntheses and processing of lysosomal cysteine proteinases in rat macrophages

E Kominami, T Tsukahara, K Hara, N Katunuma - FEBS letters, 1988 - Elsevier
E Kominami, T Tsukahara, K Hara, N Katunuma
FEBS letters, 1988Elsevier
The intracellular processing and release of three lysosomal cysteine proteinases, cathepsin
B, H and L, by rat peritoneal macrophages were investigated by pulse-chase experiments.
Newly synthesized procathepsins B (39 kDa), H (41 kDa) and L (39 kDa) after 15 min
labeling were processed to the mature, single-chain enzymes within 1 h. The single-chain
forms of cathepsin B, H and L were further processed to two-chain forms at different rates:
conversion of cathepsin L to the two-chain form was rapid, whereas the conversions …
Abstract
The intracellular processing and release of three lysosomal cysteine proteinases, cathepsin B, H and L, by rat peritoneal macrophages were investigated by pulse-chase experiments. Newly synthesized procathepsins B (39 kDa), H(41 kDa) and L (39 kDa) after 15 min labeling were processed to the mature, single-chain enzymes within 1 h. The single-chain forms of cathepsin B, H and L were further processed to two-chain forms at different rates: conversion of cathepsin L to the two-chain form was rapid, whereas the conversions cathepsin B and H took at least 6 h. Macrophages released 30% of the procathepsins B and L, and 10% of the procathepsin H.
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