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The Keap1-Nrf2 pathway is a major upstream regulator of xenobiotic detoxification. In Drosophila, directed activation of the protein complex of Keap1 and CncC (the homolog of human Nrf2) in principal and stellate cells of the Malpighian (renal) tubules confers resistance to lethal doses of the pesticide malathion, which is metabolized into organic anions. Dietary exposure to organic anions such as salicylate (10 mM) causes increases in fluid secretion rate and salicylate flux across Malpighian (renal) tubules. Here we used salicylate-selective microelectrodes and Ramsay assays to determine the role of Keap1/CncC in regulating these responses. Fluid secretion rate and salicylate flux across tubules isolated from adults with directed activation of Keap1/CncC in the principal cells are comparable to the values from salicylate-fed controls. Fluid secretion rate, concentration of salicylate in the secreted fluid and salicylate flux did not differ significantly between tubules isolated from adults with directed activation of Keap1/CncC in the principal cells reared on a diet containing salicylate and those reared on control media, indicating that the detoxification pathway was activated regardless of the presence of dietary salicylate. This is in contrast to the significant increase in fluid secretion rate and salicylate flux between tubules isolated from salicylate-fed adults and adults reared on a control diet with directed activation of Keap1/CncC in the stellate cells, supporting previous studies that demonstrated the inability of stellate cells to transport organic anions. Taken together, these results suggest a role for Keap1/CncC in upregulating fluid secretion in response to the presence of dietary organic anions. / Thesis / Master of Science (MSc) / The Keap1-Nrf2 pathway is a major upstream regulator of xenobiotic detoxification. In Drosophila, directed activation of the protein complex of Keap1 and CncC (the Nrf2 homolog) in principal and stellate cells of the Malpighian (renal) tubules confers resistance to lethal doses of the pesticide malathion, which is metabolized into organic anions. Dietary exposure to organic anions such as salicylate (10 mM) causes increases in fluid secretion rate and salicylate flux across Malpighian (renal) tubules that are comparable to tubules isolated from adults with activated Keap1/CncC reared on a salicylate-free diet. This suggests a role for Keap1/CncC in upregulating fluid secretion in response to the presence of dietary organic anions.

Wang Jian Bin. / Thesis (Ph.D.)--Chinese University of Hong Kong, 1993. / Includes bibliographical references (leaves 117-131). / ACKNOWLEDGEMENTS --- p.ii / ABSTRACT --- p.x / Chapter PART I. --- GENERAL INTRODUCTION --- p.4 / Chapter PART II. --- LITERATURE REVIEW --- p.6 / Chapter A. --- The structure and functions of insect Malpighian tubules --- p.6 / Chapter I. --- The excretory system of insects --- p.6 / Chapter 1. --- Morphology of Malpighian tubules --- p.6 / Chapter 2. --- Common types of Malpighian tubule system --- p.7 / Chapter 3. --- Morphology of hindgut --- p.8 / Chapter II. --- Structure of insect Malpighian tubules --- p.9 / Chapter 1. --- General organization of the Malpighian tubules --- p.9 / Chapter 2. --- Structure of the principal cell --- p.10 / Chapter 3. --- The structure of other cell types --- p.14 / Chapter 4. --- The cryptonephridial systems in larvae of Lepidoptera and Coleoptera --- p.16 / Chapter III. --- Functions of insect Malpighian tubules --- p.18 / Chapter 1. --- Mechanism of fluid secretion by Malpighian tubules --- p.18 / Chapter 1.1. --- Ion transport --- p.18 / Chapter 1.2. --- Fluid transport --- p.19 / Chapter 2. --- Active transport of organic compounds by Malpighian tubules --- p.19 / Chapter 2.1. --- Organic anions --- p.19 / Chapter 2.2. --- Organic cations --- p.20 / Chapter 3. --- Resporptive processes in Malpighian tubules --- p.20 / Chapter 3.1. --- KC1 resorption --- p.20 / Chapter 3.2. --- Reabsorption of sugars --- p.21 / Chapter 4. --- The passive permeability of Malpighian tubules --- p.21 / Chapter B. --- The biology and mode of action of Bacillus thuringiensis --- p.23 / Chapter I. --- Introduction --- p.23 / Chapter II. --- Background --- p.23 / Chapter III. --- "Cytology of germination, outgrowth and sporulation" --- p.24 / Chapter IV. --- Bacillus thuringiensis and its toxins --- p.26 / Chapter V. --- Histopathological effects of Bacillus thuringiensis δ-endotoxin on Lepidopterous larva --- p.29 / Chapter VI. --- Mode of action of Bacillus thuringiensis δ-endotoxin --- p.32 / Chapter C. --- The biology and pathological effects of microsporidian protozoa --- p.36 / Chapter I. --- Life cycle of microsporidian protozoa --- p.36 / Chapter II. --- Germination of microsporidian protozoa --- p.37 / Chapter III. --- The fine structure of microsporidian protozoa --- p.38 / Chapter IV. --- Mass production and storage --- p.42 / Chapter V. --- Pathology of microsporidian protozoa --- p.44 / Chapter PART III. --- LIGHT AND ELECTRON MICROSCOPIC STUDIES OF THE MALPIGHIAN TUBULES OF PIERIS CANIDIA LARVA (LEPIDOPTERA) --- p.48 / Summary --- p.48 / Introduction --- p.48 / Materials and methods --- p.49 / Results --- p.50 / Discussion --- p.53 / Chapter PART IV. --- HISTOCHEMICAL STUDIES ON THE PIERIS CANIDIA LARVAL MALPIGHIAN TUBULES --- p.58 / Summary --- p.58 / Introduction --- p.59 / Materials and methods --- p.60 / Results --- p.52 / Discussion --- p.66 / Chapter PART V. --- SEPARATION AND PURIFICATION OF PARASPORAL CRYSTALS OF BACILLUS THURINGIENSIS VAR. KURSTAKI --- p.70 / Summary --- p.70 / Introduction --- p.70 / Materials and methods --- p.74 / Results --- p.77 / Discussion --- p.77 / Chapter PART VI. --- HISTOPATHOLOGICAL EFFECTS OF BACILLUS THURINGIENSIS VAR. KURSTAKI δ-ENDOTOXIN ON THE MALPIGHIAN TUBULES OF PIERIS CANIDIA LARVA --- p.79 / Summary --- p.79 / Introduction --- p.79 / Materials and methods --- p.81 / Results --- p.83 / Discussion --- p.86 / Chapter PART VII. --- THE FINE STRUCTURE OF A MICROSPORIDIAN NOSEMA POLYVORA FROM CABBAGE WHITE PIERIS CANIDIA --- p.92 / Summary --- p.92 / Introduction --- p.92 / Materials and methods --- p.94 / Results --- p.94 / Discussion --- p.97 / Chapter PART VIII. --- HISTOPATHOLOGICAL EFFECTS OF NOSEMA POLYVORA ON THE MALPIGHIAN TUBULES OF PIERIS CANIDIA LARVA --- p.103 / Summary --- p.103 / Introduction --- p.103 / Materials and methods --- p.105 / Results --- p.105 / Discussion --- p.107 / Chapter PART IX. --- GENERAL DISCUSSION --- p.111 / Chapter PART X. --- CONCLUSION AND SUMMARY --- p.115 / REFERENCES --- p.117 / FIGURES AND TABLES --- p.132

Stimulation of urine production by the Malpighian (renal) tubules in Rhodnius prolixus is regulated by at least two diuretic hormones, CRF-related peptide and serotonin, that have traditionally been believed to function through the activation of cAMP-mediated intracellular second messenger pathways. In this study I demonstrate that serotonin stimulation triggered, in addition to cAMP, intracellular Ca2+ waves in the Malpighian tubule cells of R. prolixus. Treatment with the intracellular Ca2+ chelator BAPTA-AM blocked the intracellular Ca2+ waves and reduced serotonin-stimulated fluid secretion by 75%. This suggests a role for intracellular Ca2+ signaling in the excretory system of R. prolixus. Serotonin stimulated Malpighian tubules (MTs) exposed to Ca2+-free saline plus BAPTA-AM secreted an abnormal fluid, showing: increased K+ concentration, reduced Na+ concentration and lower pH. These results along with measurement of transepithelial potential (TEP) suggest that the basolateral Na+:K+:2Cl- cotransporter (NKCC) activity is reduced in tubule cells treated with BAPTA-AM, suggesting that Ca2+ is required to modulate the activity of the basolateral NKCC. Treatment with the non-hydrolysable cell-permeable cAMP analog, 8Br-cAMP, produced fluid with the same K+ and Na+ concentration and at the same secretion rate as serotonin-stimulated tubules. In addition, 8Br-cAMP triggered intracellular Ca2+ oscillations similar to those obtained with serotonin. 8Br-cAMP-stimulated tubules treated with BAPTA-AM decreased their fluid secretion by about 40% and increased Na+ concentration, similar to the effect observed on serotonin-stimulated tubules. Therefore, I conclude that the intracellular Ca2+ waves triggered by serotonin are mediated by cAMP. The role of inositol-3-phospate (InsP3) in Ca2+ release was tested by treating the tubules with the InsP3 receptor blocker xestospongin. The treatment decreased fluid secretion rate as well as the amplitude of Ca2+ waves in serotonin-stimulated tubules. These results suggest that serotonin activates the production of InsP3 and, most likely, diacylglycerol (DAG). Thus, I decided to test whether the protein kinase C (PKC) may be involved in serotonin-stimulated secretion. The PKC inhibitors chelerythrine and bisindolylmaleimide (BIM) decreased secretion fluid rate in serotonin-stimulated tubules by 50% and 70%, respectively. Fluid secreted by tubules treated with BIM showed no differences in K+ and Na+ concentrations compared to controls, however both ion fluxes decreased. The evidence suggests that PKC is involved in serotonin stimulated secretion; the mechanism is still not understood. Taken together, the results suggest that cAMP, Ca2+ and PLC-PKC pathway are involved in serotonin stimulated secretion. However cAMP stimulation is enough for maximal secretion rate. Therefore PLC-PKC must act downstream of cAMP. Based on those results we hypothesize that serotonin binds a GPCR, increasing cAMP by activation of an adenylate cyclase (AC). Subsequently, cAMP is somehow able to activate PLC, which finally produces Ca2+ release, PKC activation and NKCC upregulation.

The evolution of the blood feeding adaptation has required precise coordination of multiple physiological processes in the insect, such as reproduction, behavior, digestion and diuresis. These processes are under careful synchronous hormonal control. For rapid excretion, multiple diuretic hormones are known. Although originally described based on their ability to stimulate hindgut contractions, the Aedes kinins have been shown to stimulate fluid secretion in female mosquitoes of Aedes aegypti. Aedes kinins are leucokinin-like neuropeptides released from neurosecretory cells in the brain and abdominal ganglia. They act by binding to the Aedes kinin receptor, a G proteincoupled receptor (GPCR). The Aedes kinin receptor has been cloned, sequenced, functionally characterized, and immunolocalized to stellate cells in the Malpighian tubules of Ae. aegypti. In addition to their myotropic and diuretic roles, leucokinin-like peptides and/or their receptors have been also been discovered in the nervous, digestive, and reproductive systems of other arthropod species. Therefore, the Aedes kinins have the potential to function in several simultaneous physiological processes that are stimulated by blood feeding. This thesis aims to understand better their role in the whole mosquito by investigating the Aedes kinin receptor's global expression as well as its in vivo contribution to post-prandial diuresis. Presence of the Aedes kinin receptor was investigated in the head, posterior midgut (stomach), hindgut, ovaries, and Malpighian tubules of both non blood-fed and blood-fed females by western blot using anti-receptor antibodies. The receptor was then immunolocalized in the posterior midgut and rectum. Finally, RNAi was employed to knock down kinin receptor expression, followed by measurement of in vivo urine excretion post blood feeding in a precision humidity chamber. Transcript and protein knockdown were confirmed by qPCR and immunohistochemistry, respectively. Results indicate widespread expression of the Aedes kinin receptor protein in organs novel for hematophagous insects and demonstrate the receptor's fundamental role in rapid diuresis. These findings strongly point to the Aedes kinins as integrative signaling molecules that could coordinate multiple physiological systems. The Aedes kinins could therefore have contributed to the success of the blood feeding adapation in mosquitoes.

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Orientador: Maria Luiza Silveira Mello / Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Biologia / Made available in DSpace on 2018-08-07T20:32:58Z (GMT). No. of bitstreams: 1 Mampumbu_AndreRoberto_D.pdf: 659647 bytes, checksum: 40d0a48fa1d02750dffb30ae80b25445 (MD5) Previous issue date: 2006 / Resumo: O gênero Melipona (abelhas sem ferrão) tem sido dividido em dois grupos, com base no seu conteúdo em heterocromatina revelada com a técnica de banda-C em cromossomos mitóticos. Melipona quadrifasciata e Melipona rufiventris apresentam, respectivamente, níveis baixos e altos de heterocromatina. Na suposição de que cromatina condensada possa ser rica em seqüências de DNA metiladas, M. quadrifasciata e M. rufiventris poderiam então apresentar diferenças em conteúdo de seqüências CpG metiladas. Se isso acontecesse, as diferenças poderiam ser reveladas pela comparação de valores Feulgen-DNA obtidos por análise de imagem de células tratadas com as enzimas de restrição Msp I e Hpa II, que distinguem entre seqüências metiladas e não metiladas. Msp I e Hpa II clivam as seqüências ¿CCGG-, porém não há clivagem pela Hpa II se a citosina do dinucleotídeo central CG for metilada. Neste trabalho, túbulos de Malpighi de larva de último estádio de M. quadrifasciata e M. rufiventris submetidos à reação de Feulgen precedida pelo tratamento com Msp I e Hpa II tiveram suas células analisadas por microespectrofotometria de varredura automática. Para esse material houve necessidade do desenvolvimento prévio de um ajuste metodológico que tornasse a reação de Feulgen reveladora apenas de DNA, visto que ocorria reação plasmal; isto foi conseguido com um tratamento por boridreto de sódio a 5% e acetona/clorofórmio (1:1, v/v) antecedendo a reação de Feulgen. Também, embora a definição de altos e baixos conteúdos de heterocromatina em Melipona pela técnica de banda-C não fosse extensível à cromatina de núcleos interfásicos dos túbulos de Malpighi dessas abelhas, demonstrou-se que a depurinação do DNA em M. quadrifasciata era mais rápida do que a de M. rufiventris, confirmando, maiores teores de cromatina condensada em M. rufiventris. Os valores Feulgen-DNA para a heterocromatina de Melipona rufiventris e para a pouca heterocromatina somada a alguns domínios de eucromatina de Melipona quadrifasciata diminuíram após tratamento com Msp I, porém ficaram inalterados após tratamento com Hpa II. Conclui-se que seqüências CpG metiladas podem estar contidas em diferentes compartimentos cromatínicos, conforme a espécie do gênero Melipona considerada, e que os seus efeitos silenciadores possam atuar induzindo uma mesma fisiologia celular / Abstract: The genus Mellipona has been divided into two groups based on its heterochromatin content revealed by C-banding pattern in mitotic chromosomes. Melipona quadrifasciata and Melipona rufiventris show low and high heterochromatin content, respectively. Supposing that condensed chromatin may be rich in DNA methylated sequences, M quadrifasciata and M. rufiventris could, thus, show differences regarding their content of CpG methylated sequences. In this situation, such differences could be revealed by comparing the Feulgen-DNA values acquired after image analysis of cells treated with restriction enzymes Msp I and Hpa II, which distinguish between methylated and nonmethylated sequences. Msp I and Hpa II break the CCGG sequences. Nevertheless, Hpa II is ubable to break the DNA strand if the cytosine from the central nucleotide pair CG is methylated. In this work, Malpighian tubules from larvae from the last stage of M. quadrifasciata and M. rufiventris, subjected to the Feulgen reaction after by treatment with Msp I and Hpa II, were analysed in automatic scanning microspectrophotometry. Since a plasmal reaction was observed in this material, it was previously necessary the development of a methodological adjustement to make the Feulgen reaction specific to DNA. This was achieved by treatment of material with 5% sodium borohydrade followed by acetone-chloroform (1:1, v/v) before the Feulgen reaction. Also, although the definition of high and low heterochromatin content in Melipona after C-banding technique is not applicable to the chromatin of interphasic nuclei in Malpighian tubules of bees, it was demonstrated that DNA depurination in M. quadrifasciata was faster than that of M. rufiventris, thus confirming that this species has a higher condensed chromatin content. The Feulgen-DNA values for the heterochromatin of Melipona rufiventris, and for the heterochromatin besides some euchromatic domains of Melipona quadrifasciata, decreased after treatment with Msp I, remaining, however, unaltered after treatment with Hpa II. In conclusion, methylated CpG sequences may be part of different chromatin compartments, according to the considered species of the genus Melipona, and that their silencing effects may act by inducing the same cell physiology / Doutorado / Biologia Celular / Doutor em Biologia Celular e Estrutural

<p>Insects are continually exposed to potentially toxic endogenous compounds and xenobiotics that require rapid elimination from the body. Xenobiotic resistance in insects has evolved predominantly by increasing the activity of detoxification enzymes and/or by increasing toxin excretion via the Malpighian (renal) tubules. The tubules have long been known to transport organic anions at high rates. This thesis examines the mechanisms of excretion and detoxification of the organic anion methotrexate (MTX) by isolated tissues of the fruit fly <em>Drosophila melanogaster</em>. A radioisotope tracer technique and the Ramsay assay were used to measure MTX secretion. Quantitative PCR (qPCR) was used to evaluate the expression of the genes for putative organic anion transporters. My results show that MTX transport across the Malpighian tubule epithelium is active, saturable, Na⁺-independent and inhibited by a wide range of organic anions including MK-571, probenecid and Texas Red. Pharmacological studies and qPCR analyses suggest multiple transporters are involved in the movement of MTX across the Malpighian tubules. Moreover, chronic exposure of larvae to dietary MTX or salicylate dramatically increases the transepithelial transport of MTX by isolated Malpighian tubules, suggesting that excretion of MTX is upregulated by exposure to these organic anions in the diet. In addition, treatments known to increase expression of specific detoxification enzymes, such as the P450 monoxygenases (P450s) and the glutathione-S-transferases (GSTs), also led to an increase in expression levels of multidrug efflux transporter (MET), multidrug resistance like protein 1 (dMRP) as well as to increased secretion of MTX by the tubules. This latter finding suggests a coordinated response to toxin exposure, so that when detoxification pathways are increased, there is a corresponding increase in the capacity for elimination of the products of P450 and GST enzymes. Finally, the last section of this thesis has shown that RNAi knockdown of a single organic anion transporter gene in the principal cells of <em>D. melanogaster</em> Malpighian tubules is associated with reductions in the expression of multiple, functionally-related genes. Importantly, these results indicate that dMRP andMET are not the dominantMTX transporters in the tubules when flies are reared onMTX-enriched diets. However, reductions in the expression of organic anion transporting polypeptide (OATP) are associated with reduced secretion of the organic anionsMTX, fluorescein and Texas Red. Taken together, these results suggest that OATP and at least one additional transporter, as yet unidentified, are required forMTX secretion. In conclusion, the results of my research contribute to our understanding of the mechanisms of organic anion detoxification and excretion in flies exposed to dietary toxins.</p> / Doctor of Science (PhD)

Insect haemolynph typically contains very high levels of free amino acids 50 1 00 times that which is normal for mammalian plasma. This study examines the modulatory effects of amino acids on fluid secretion and ion transport by isolated MTs of Rhodnius prolixus and Drosophila melanogaster. The results show that the secretion rates of isolated Malpighian tubules of both Rhodnius and Drosophila are modulated by the presence of specific amino acids in the bathing saline. Some amino acids are stimulatory, some are inhibitory and others have little or no effect. Glutamine appears to be particularly important as a stimulant of fluid secretion. As well, secreted fluid pH and Na +concentration increase and K+ concentration decreases in response to glutamine. Amino acids do not appear to be important as metabolite. in Rhodnius tubules, nor do they act to draw significant amounts of water into the lumen by osmosis. Significant stimulation of fluid secretion can be achieved by physiological levels of particular amino acids, whereas those amino acids that inhibit fluid secretion only do so at concentrations much above those at which they occur naturally in the haemolymph. Amino acids are known to be compatible osmolytes and may be acting to maintain cell homeostasis and thus to sustain fluid secretion. The passive movement of amino acids may result in cell volume changes, and some form of osmosensor is may be coupled to activation of specific kinases to produce the observed increases in fluid secretion. The effects of several kinase inhibitors were therefore examined. The glutamine dependent increase in MT fluid secretion is blocked by two inhibitors of the stress activated protein kinase (SAPK) pathway, SP600125 and dicumoral. Inhibitors of other kinases (PKA, PKC, PKG, PI-3, p38, ERK and MEK), did not block glutamine's effects on fluid secretion rate. Alterations in cytoskeletal structure appear not to be required because cytoskeletal disrupting agents did not block the glutamine dependent inc~ease in fluid secretion, nor was the increase dependent upon protein synthesis. Results of this study are the first to suggest a role for the SAPK pathway in the control of fluid secretion rates by insect Malpighian tubules. / Thesis / Master of Science (MS)

G protein-coupled receptors (GPCRs) are composed of seven transmembrane domains and play an essential role in regulating physiological functions and mediating responses to environmental stimuli, biogenic amines, neurotransmitters, peptides, lipids, and hormones. The calcitonin-like diuretic hormone 31 (DH31) is known to elicit natriuresis from the Malpighian tubules (MTs) of mosquitoes Anopheles gambiae and Aedes aegypti upon blood feeding. However, the contribution of DH31 cognate receptor, calcitonin receptor 1 (GPRCAL1), has not been evaluated with respect to postprandial fluid regulation or myostimulatory activity in blood feeding insects. Thus, this dissertation has investigated potential roles of AedaeGPRCAL1 in the regulation of fluid homeostasis and hindgut muscle contraction in female A. aegypti mosquito. The full length cDNA encoding AedaeGPRCAL1 was cloned and sequenced. The receptor expression in the MTs and hindgut from female mosquito was analyzed by western blot and immunohistochemistry using anti-AedaeGPRCAL1 affinity purified antibodies, and subsequently its role in fluid transport and hindgut contraction was evaluated by RNA interference (RNAi). The mosquitoes that underwent knock-down of the AedaeGPRcal1 exhibited up to 57% lower rate of MT fluid secretion in presence of Aedae-DH31 in the in vitro assay and a ~30% reduction in the fluid excreted from live females upon blood feeding. The receptor was immunolocalized in principal cells, predominantly towards the distal end of MTs. Analyses of receptor signal probability indicate the receptor is expressed in a gradient-like fashion along the length of the MTs. A striking discovery was the fact that not all principal cells express the receptor, contrary to previous belief. Immunolocalization revealed the AedaeGPRCAL1 is expressed in hindgut circular and longitudinal muscles. The application of DH31 increased the frequency of hindgut contractions in all female mosquitoes, those injected with AedaeGPRcal1 dsRNA and controls, as compared to their basal contraction rate, but the percent change in frequency of hindgut contraction from AedaeGPRcal1 knock-down females was about 2-fold lower than the controls after application of Aedae-DH31. To my knowledge, this is first evidence of RNAi-induced phenotypes in any invertebrate that allowed the quantification of the contribution of single family B GPCR to fluid loss and muscle contractility.