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Higher expression of proline dehydrogenase altered mitochondrial function and increased Trypanosoma cruzi differentiation in vitro and in the insect vector

https://doi.org/10.1042/bcj20210428

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/bf00763064openalex-snapshot

Intermediate metabolism inTrypanosoma cruzi

inferredcites →https://doi.org/10.1007/s10863-011-9365-4openalex-snapshot

Role of Trypanosoma cruzi peroxiredoxins in mitochondrial bioenergetics

inferredcites →https://doi.org/10.1016/0003-2697(76)90223-2openalex-snapshot

Properties and analysis of a stable derivative of pyrroline-5-car☐ylic acid for use in metabolic studies

inferredcites →https://doi.org/10.1016/0005-2728(90)90099-popenalex-snapshot

Calcium inhibition of the ATP ⇌ [32P]Pi exchange and of net ATP synthesis catalyzed by bovine submitochondrial particles

inferredcites →https://doi.org/10.1016/0166-6851(85)90073-8openalex-snapshot

In vitro differentiation of Trypanosoma cruzi under chemically defined conditions

inferredcites →https://doi.org/10.1016/0305-0491(76)90318-7openalex-snapshot

Proline metabolism in Trypanosoma cruzi epimastigotes

inferredcites →https://doi.org/10.1016/b978-0-12-152825-6.50008-4openalex-snapshot

The Regulatory Functions of Proline and Pyrroline-5-carboxylic Acid

inferredcites →https://doi.org/10.1016/j.abb.2004.07.025openalex-snapshot

Detection of hydrogen peroxide with Amplex Red: interference by NADH and reduced glutathione auto-oxidation

inferredcites →https://doi.org/10.1016/j.abb.2012.02.020openalex-snapshot

Tryparedoxin peroxidases and superoxide dismutases expression as well as ROS release are related to Trypanosoma cruzi epimastigotes growth phases

inferredcites →https://doi.org/10.1016/j.bbrc.2004.07.002openalex-snapshot

Post genomic analysis of permeases from the amino acid/auxin family in protozoan parasites

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2009.04.020openalex-snapshot

Modulation of Trypanosoma rangeli ecto-phosphatase activity by hydrogen peroxide

inferredcites →https://doi.org/10.1016/j.molbiopara.2009.07.006openalex-snapshot

Glucose uptake in the mammalian stages of Trypanosoma cruzi

inferredcites →https://doi.org/10.1016/j.molbiopara.2018.07.007openalex-snapshot

L-Glutamine uptake is developmentally regulated and is involved in metacyclogenesis in Trypanosoma cruzi

inferredcites →https://doi.org/10.1016/s0021-9258(18)99229-xopenalex-snapshot

ATP in equilibrium with 32Pi exchange catalyzed by plasma membrane Ca(2+)-ATPase from kidney proximal tubules

inferredcites →https://doi.org/10.1016/s0034-5687(01)00307-3openalex-snapshot

Bioenergetics at low oxygen: dependence of respiration and phosphorylation on oxygen and adenosine diphosphate supply

inferredcites →https://doi.org/10.1016/s0065-2806(09)37004-6openalex-snapshot

Chapter 4 Interactions of Trypanosomatids and Triatomines

inferredcites →https://doi.org/10.1016/s0140-6736(17)31612-4openalex-snapshot

Chagas disease

inferredcites →https://doi.org/10.1016/s0166-6851(02)00277-3openalex-snapshot

Regulatory volume decrease in Trypanosoma cruzi involves amino acid efflux and changes in intracellular calcium

inferredcites →https://doi.org/10.1016/s0378-1097(99)00646-1openalex-snapshot

Separation of NADH-fumarate reductase and succinate dehydrogenase activities in Trypanosoma cruzi

inferredcites →https://doi.org/10.1017/s0031182000070554openalex-snapshot

Studies of the amino acids of Rhodnius prolixus . I. Analysis of the haemolymph

inferredcites →https://doi.org/10.1038/ncomms3865openalex-snapshot

Essential regulation of cell bioenergetics in Trypanosoma brucei by the mitochondrial calcium uniporter

inferredcites →https://doi.org/10.1042/bcj20200232openalex-snapshot

Trypanosoma cruzi synthesizes proline via a Δ1-pyrroline-5-carboxylate reductase whose activity is fine-tuned by NADPH cytosolic pools

inferredcites →https://doi.org/10.1056/nejmra1410150openalex-snapshot

Chagas’ Disease

inferredcites →https://doi.org/10.1074/jbc.m109.009340openalex-snapshot

Unraveling Δ1-Pyrroline-5-Carboxylate-Proline Cycle in Plants by Uncoupled Expression of Proline Oxidation Enzymes

inferredcites →https://doi.org/10.1074/jbc.m114.574525openalex-snapshot

Role of Δ1-Pyrroline-5-Carboxylate Dehydrogenase Supports Mitochondrial Metabolism and Host-Cell Invasion of Trypanosoma cruzi

inferredcites →https://doi.org/10.1074/jbc.m117.778522openalex-snapshot

Metabolomic profiling reveals a finely tuned, starvation-induced metabolic switch in Trypanosoma cruzi epimastigotes

inferredcites →https://doi.org/10.1074/jbc.m410372200openalex-snapshot

Acidocalcisomes and the Contractile Vacuole Complex Are Involved in Osmoregulation in Trypanosoma cruzi

inferredcites →https://doi.org/10.1074/jbc.m414274200openalex-snapshot

Proline Metabolism in Procyclic Trypanosoma brucei Is Down-regulated in the Presence of Glucose

inferredcites →https://doi.org/10.1080/21505594.2020.1797274openalex-snapshot

Transcriptional remodeling during metacyclogenesis in Trypanosoma cruzi I

inferredcites →https://doi.org/10.1089/ars.2017.7350openalex-snapshot

Proline Metabolism in Cell Regulation and Cancer Biology: Recent Advances and Hypotheses

inferredcites →https://doi.org/10.1093/nar/20.15.3963openalex-snapshot

A shuttle vector which facilitates the expression of transfected genes inTrypanosoma cruzi and Leishmania

inferredcites →https://doi.org/10.1111/j.1462-5822.2004.00397.xopenalex-snapshot

l-Proline is essential for the intracellular differentiation of Trypanosoma cruzi

inferredcites →https://doi.org/10.1111/j.1550-7408.1989.tb01063.xopenalex-snapshot

Some Factors Inducing Formation of Metacyclic Stages of Trypanosoma cruzi

inferredcites →https://doi.org/10.1111/j.1550-7408.2002.tb00225.xopenalex-snapshot

Active Transport of L‐Proline in Trypanosoma cruzi

inferredcites →https://doi.org/10.1128/iai.00138-09openalex-snapshot

Use of l -Proline and ATP Production by Trypanosoma cruzi Metacyclic Forms as Requirements for Host Cell Invasion

inferredcites →https://doi.org/10.1152/physrev.00018.2001openalex-snapshot

Free Radicals in the Physiological Control of Cell Function

inferredcites →https://doi.org/10.1242/jeb.87.1.315openalex-snapshot

The Retention of Amino Acids in the Haemolymph During Diuresis in Rhodnius

inferredcites →https://doi.org/10.1371/journal.pntd.0004186openalex-snapshot

Monitoring of the Parasite Load in the Digestive Tract of Rhodnius prolixus by Combined qPCR Analysis and Imaging Techniques Provides New Insights into the Trypanosome Life Cycle

inferredcites →https://doi.org/10.1371/journal.pone.0004534openalex-snapshot

Actions of a Proline Analogue, L-Thiazolidine-4-Carboxylic Acid (T4C), on Trypanosoma cruzi

inferredcites →https://doi.org/10.1371/journal.pone.0069419openalex-snapshot

Proline Dehydrogenase Regulates Redox State and Respiratory Metabolism in Trypanosoma cruzi

inferredcites →https://doi.org/10.1371/journal.pone.0092028openalex-snapshot

Proline Modulates the Trypanosoma cruzi Resistance to Reactive Oxygen Species and Drugs through a Novel D, L-Proline Transporter

inferredcites →https://doi.org/10.1371/journal.pone.0116712openalex-snapshot

Proliferation and Differentiation of Trypanosoma cruzi inside Its Vector Have a New Trigger: Redox Status

inferredcites →https://doi.org/10.1371/journal.ppat.1006158openalex-snapshot

Proline Metabolism is Essential for Trypanosoma brucei brucei Survival in the Tsetse Vector

inferredcites →https://doi.org/10.1371/journal.ppat.1009495openalex-snapshot

Fatty acid oxidation participates in resistance to nutrient-depleted environments in the insect stages of Trypanosoma cruzi

inferredcites →https://doi.org/10.2174/138161211796904786openalex-snapshot

The Uniqueness of the Trypanosoma cruzi Mitochondrion: Opportunities to Target New Drugs Against Chagas Disease

inferredcites →https://doi.org/10.3389/fcimb.2020.00027openalex-snapshot

The Influence of Environmental Cues on the Development of Trypanosoma cruzi in Triatominae Vector

inferredcites →https://doi.org/10.3390/pathogens7020036openalex-snapshot

The Uptake and Metabolism of Amino Acids, and Their Unique Role in the Biology of Pathogenic Trypanosomatids

inferredcites →https://doi.org/10.4061/2011/486928openalex-snapshot

The Involvement of Glutamate Metabolism in the Resistance to Thermal, Nutritional, and Oxidative Stress in Trypanosoma cruzi

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4529480openalex-extracted

The Branched Chain Amino Acids (BCAAs) Modulate the Intracellular Differentiation Processes in Trypanosoma Cruzi

inferred← citeshttps://doi.org/10.1016/j.exppara.2023.108642openalex-snapshot

The branched chain amino acids (BCAAs) modulate the development of the intra-cellular stages of Trypanosoma cruzi

inferred← citeshttps://doi.org/10.1101/2024.04.17.589966openalex-snapshot

Branched chain amino acids modulate the proteomic profile of Pro-induced differentiation for the infective stages of Trypanosoma cruzi

inferred← citeshttps://doi.org/10.1111/febs.70030openalex-snapshot

Genetic and functional dissection of the glutamate‐proline pathway reveals a shortcut for glutamate catabolism in Leishmania

inferred← citeshttps://doi.org/10.1111/jeu.12911openalex-snapshot

Mitochondrial adaptations throughout the Trypanosoma brucei life cycle

inferred← citeshttps://doi.org/10.1128/mbio.02215-24openalex-snapshot

Energy metabolism in Trypanosoma cruzi : the validated and putative bioenergetic and carbon sources

inferred← citeshttps://doi.org/10.1186/s13071-025-06966-xopenalex-snapshot

Proline dehydrogenase, a rate-limiting catabolic enzyme, affecting the growth and pathogenicity of Toxoplasma gondii tachyzoites by regulating the proline metabolism and mitochondrial function of the parasite

inferred← citeshttps://doi.org/10.1371/journal.pntd.0012588openalex-snapshot

Branched-chain amino acids modulate the proteomic profile of Trypanosoma cruzi metacyclogenesis induced by proline

inferred← citeshttps://doi.org/10.1371/journal.ppat.1012012openalex-snapshot

Small molecule mediators of host-T. cruzi-environment interactions in Chagas disease

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