An improved procedure for the isolation of lamellar bodies from human lung. Lamellar bodies free of lysosomes contain a spectrum of lysosomal-type hydrolases
Publication date
1987-12-14
Authors
Vries, A.C.J. de
Schram, A.W.
Berg, Marlene van den
Tager, J.M.
Batenburg, J.J.
Golde, L.M.G. van
Editors
Advisors
Supervisors
DOI
Document Type
Article
Metadata
Show full item recordCollections
License
Abstract
We have recently shown that lamellar body fractions purified from human lung contain a distinct acid
α-glucosidase distinguishable from lysosomal acid α-glucosidase in that it does not cross-react with
antibodies raised against the lysosomal enzyme and does not bind to concanavalin A. In order to study the relationship between the non-concanavalin A-binding α-glueosidase and
lamellar bodies more closely a method was developed for the further purification of the organelles. A
purified lamelar body preparation isolated from human lung homogenate by discontinuous sucrose density
centrifugation was subjected to gel filtration with Sepharose 4B followed by Percoli density gradient
centrifugation, which yielded a lamellar body preparation with a phospholipid phosphorus/protein ratio of
12.57 ± 0.38 (µmol/mg) (n = 3) as compared to a ratio of 3.34 ± 0.16 (µmol/mg) (n = 3) in the sucrose
density gradient preparation. Concomitantly there was a 3.3 ± 0.1 (n = 3) -fold enrichment in the content of
total acid α-glutosidase and a 3.2 ± 0.1 (n = 3) -fold enrichment of non-concanavalin A-binding acid
α-glucosidase. The new purification method removes adhering proteins without changing the phospholipid
composition. During the successive purification steps the concanavalin A-sensitive and -insensitive α-glucosidases
remained fully lamellar body fraction associated. Differences between a lysosome-enriched fraction
and a lamellar body preparation at varying stages of purification with respect to the ratio between soluble
acid hydrdases and the membrane-associate lysosomal enzyme glucocerebrosidase indicate that the
purified lamellar bodies were not contaminated with lysosomes. The absence of lysosomes in the purified
lamellar body fraction was confirmed by experiments with the weak base glycyl-L-phenylalanine-β-naphthylamide,
which is an artificial substrate for the lysosomal enzyme cathepsin C and brings about lysis of
lysosomes. Morphological examination by electron microscopy endorses the absence of contaminating
vesicles and organelles and showed a structural integrity of the lamellar bodies in the final preparation. The improved isolation procedure strongly suggests that the concanavalin A-insensitive acid α-glucosidase is
endogenous to lamellar bodies and supports our earlier idea that it can be used as a lamellar body-specific
marker enzyme. In addition, the experiments show that lamellar bodies free of lysosomes contain a spectrum
of lysosomal-type enzymes.
Keywords
Lamellar body, Lysosomal enzyme, [alpha]-Glucosidase, Pulmonary surfactant, (Human lung), lamellar body, lysosomal enzyme, α-Glucosidase, pulmonary surfactant, (human lung)