1994•Journal of Experimental BiologyRequires access

The MalpighianC Tubules Of Drosophila Melanogaster : A Novel Phenotype For Studies Of Fluid Secretion And Its Control

Julian A. T. Dow, Simon H. P. Maddrell, Andreas Görtz, Nick Skaer, Scott Brogan, Kim Kaiser

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Abstract

ABSTRACT The insect renal (Malpighian) tubule has long been a model system for the study of fluid secretion and its neurohormonal control (Maddrell, 1981; Maddrell and O’Donnell, 1992). Classical physiology suggests a model for tubular secretion of iso-osmotic fluid in most insects, in which ions are thought to enter basally either through a series of ion channels (Na+, K+ and Cl−) or through a bumetanide-sensitive Na+/K+/2Cl− cotransport. Apical fluxes are energised by a plasma-membrane H+-pumping V-ATPase, driving secretion of Na+ or K+ through one or more exchangers, at least one of which is amiloride-sensitive and appears to be closely similar to the Na+/H+ exchanger of vertebrates (Maddrell and O’Donnell, 1992). Cl− follows passively, perhaps through apical Cl− channels. Water follows the major ions, and haemolymph solutes diffuse across the tubule wall passively via a paracellular route. There are also transcellular active transport processes for certain metabolites or toxins, such as acylamides (Maddrell et al. 1974) and plant alkaloids (Maddrell, 1976; O’Donnell et al. 1983).

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What this paper is about

ABSTRACT The insect renal (Malpighian) tubule has long been a model system for the study of fluid secretion and its neurohormonal control (Maddrell, 1981; Maddrell and O’Donnell, 1992). Classical physiology suggests a model for tubular secretion of iso-osmotic fluid in most insects, in which ions are thought to enter basally either through a series of ion channels (Na+, K+ and Cl−) or through a bumetanide-sensitive Na+/K+/2Cl− cotransport. Apical fluxes are energised by a plasma-membrane H+-pumping V-ATPase, driving secretion of Na+ or K+ through one or more exchangers, at least one of which is amiloride-sensitive and appears to be closely similar to the Na+/H+ exchanger of vertebrates (Maddrell and O’Donnell, 1992). Cl− follows passively, perhaps through apical Cl− channels. Water follows the major ions, and haemolymph solutes diffuse across the tubule wall passively via a paracellular route. There are also transcellular active transport processes for certain metabolites or toxins, such as acylamides (Maddrell et al. 1974) and plant alkaloids (Maddrell, 1976; O’Donnell et al. 1983).

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Available abstract

ABSTRACT The insect renal (Malpighian) tubule has long been a model system for the study of fluid secretion and its neurohormonal control (Maddrell, 1981; Maddrell and O’Donnell, 1992). Classical physiology suggests a model for tubular secretion of iso-osmotic fluid in most insects, in which ions are thought to enter basally either through a series of ion channels (Na+, K+ and Cl−) or through a bumetanide-sensitive Na+/K+/2Cl− cotransport. Apical fluxes are energised by a plasma-membrane H+-pumping V-ATPase, driving secretion of Na+ or K+ through one or more exchangers, at least one of which is amiloride-sensitive and appears to be closely similar to the Na+/H+ exchanger of vertebrates (Maddrell and O’Donnell, 1992). Cl− follows passively, perhaps through apical Cl− channels. Water follows the major ions, and haemolymph solutes diffuse across the tubule wall passively via a paracellular route. There are also transcellular active transport processes for certain metabolites or toxins, such as acylamides (Maddrell et al. 1974) and plant alkaloids (Maddrell, 1976; O’Donnell et al. 1983).

Key concepts: Transcellular, Tubule, Bumetanide, Malpighian tubule system, Paracellular transport, Secretion, Biophysics, Cotransporter

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