The University of Osaka · Medicine
Professor Shiroh Iwanaga's research lab specializes in molecular parasitology and host-pathogen interactions, with a focus on understanding the innate immune mechanisms in invertebrates and the molecular regulation of malaria parasite development. The lab investigates novel anticoagulant and immunomodulatory molecules from ticks and other arthropods, exploring their potential as therapeutic leads. Additionally, the lab develops advanced molecular tools, such as Plasmodium artificial chromosomes, to study gene regulation and chromosome dynamics in malaria parasites. These interdisciplinary efforts bridge parasitology, structural biology, and biotechnology to address infectious diseases.
Figures are computed from collected data and may differ slightly.
Invertebrate animals, which lack adaptive immune systems, have developed defense systems, so-called innate immunity, that respond to common antigens on the surface of potential pathogens. One such defense system is involved in the cellular responses of horseshoe crab hemocytes to invaders. Hemocytes contain two types, large (L) and small (S), of secretory granules, and the contents of these granules are released in response to invading microbes via exocytosis. Recent biochemical and immunologica
Two N-terminal fragments of α(A)-chain and β(B)-chain in human fibrinogen have been isolated from a plasmic hydrolyzate. The fragment from the α(A)-chain consisted of 43 amino acid residues including two half-cystine residues. On treatment with thrombin, this fragment produced two other peptides in addition to fibrinopeptide A and its analogues. One was a tripeptide, Gly-Pro-Arg, and the other a peptide containing 24 amino acid residues having N-terminal valine. The partial amino acid sequence o
Liver-stage malaria parasites are a promising target for drugs and vaccines against malaria infection. However, little is currently known about gene regulation in this stage. In this study, we used the rodent malaria parasite Plasmodium berghei and showed that an AP2-family transcription factor, designated AP2-L, plays a critical role in the liver-stage development of the parasite. AP2-L-depleted parasites proliferated normally in blood and in mosquitoes. However, the ability of these parasites
Novel antithrombin molecules were identified from the ixodidae tick, Haemaphysalis longicornis. These molecules, named madanin 1 and 2, are 7-kDa proteins and show no significant similarities to any previously identified proteins. Assays using human plasma showed that madanin 1 and 2 dose-dependently prolonged both activated partial thromboplastin time and prothrombin time, indicating that they inhibit both the intrinsic and extrinsic pathways. Direct binding assay by surface plasmon resonance m
The artificial chromosome represents a useful tool for gene transfer, both as cloning vectors and in chromosome biology research. To generate a Plasmodium artificial chromosome (PAC), we had to first functionally identify and characterize the parasite's centromere. A putative centromere (pbcen5) was cloned from chromosome 5 of the rodent parasite P. berghei based on a Plasmodium gene-synteny map. Plasmids containing pbcen5 were stably maintained in parasites during a blood-stage infection with h
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