Changes in lipoprotein composition during larval-pupal metamorphosis of an insect, Manduca sexta

• Published in: The Journal of biological chemistry Vol. 261; no. 2; pp. 558 - 562
• Main Authors: Prasad, S V, Ryan, R O, Law, J H, Wells, M A
• Format: Journal Article
• Language: English
• Published: Bethesda, MD Elsevier Inc 15.01.1986; American Society for Biochemistry and Molecular Biology
• Subjects: Animals; Apolipoproteins - analysis; Applied sciences; Biological and medical sciences; Carrier Proteins - analysis; Electrophoresis, Polyacrylamide Gel; Exact sciences and technology; Fundamental and applied biological sciences. Psychology; Hemolymph - analysis; Insecta; Invertebrates; Larva; Lepidoptera - physiology; Life cycle. Embryology. Development; Lipoproteins - analysis; Metamorphosis, Biological; Other techniques and industries; Physiology. Development; Ultracentrifugation; Arthropoda; Insecta; Lepidoptera; Chemical composition; Lipoprotein; Invertebrata; Sphingidae; Metamorphosis
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/S0021-9258(17)36128-8

During the transition from the last feeding larval stage to the pupal stage of the tobacco hornworm, Manduca sexta, significant changes occur in the properties of lipophorin, the major hemolymph lipoprotein. Within the first 24 h after cessation of feeding, the larval lipophorin (HDLp-L) is first converted to a higher density form (HDLp-W2) and then HDLp-W2 is converted to a lower density form (HDLp-W1). HDLp-W1 remains in the hemolymph until pupation, when another form, HDLp-P, with a density between HDLp-W1 and HDLp-L, is present. Although all the lipophorins contain identical apoproteins, they differ in lipid content and composition; the differences in density being primarily related to diacylglycerol content. The conversion of HDLp-L to HDLp-W1 is accompanied by a loss of hydrocarbon and uptake of carotenes. These latter changes in lipophorin composition reflect alterations in cuticular lipid composition. HDLp-L was radiolabeled in the apoproteins by injecting animals with 3H-amino acids early in the last larval stage. Subsequently HDLp-L was isolated at the end of the larval stage, HDLp-W2 and HDLp-W1 were isolated during the wandering stage, and HDLp-P was isolated after pupation. The specific activity of the apoproteins in the four lipophorins was not significantly different, suggesting that the observed alterations in lipophorin properties do not require synthesis of new apoproteins but result from retailoring the lipid composition of preexisting molecules. Examination of the hemolymph of individual animals during these transitions showed that only one species of lipoprotein was present, never a mixture of two or more species. These observations suggest that the lipoprotein conversions are precisely timed and that lipoprotein metabolism during larval development and pupation cannot be considered a static process. The unique finding of these studies was that synthesis of lipophorin apoproteins proceeds actively during the first part of the fifth instar but then ceases and does not recommence during the wandering or early pupal stages.