Publications by authors named "Wakamiya N"

Cyborg insects refer to hybrid robots that integrate living insects with miniature electronic controllers to enable robotic-like programmable control. These creatures exhibit advantages over conventional robots in adaption to complex terrain and sustained energy efficiency. Nevertheless, there is a lack of literature on the control of multi-cyborg systems.

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  • * Out of 17 participants, TMA symptoms appeared within 72 hours post-transplant, with 16 cases involving ABO incompatibility, and the usage of pre-transplant plasmapheresis was found to be low.
  • * Although some gene variants related to TMA were identified in Japanese and East Asian patients, most cases did not lead to significant complications, suggesting that further research is needed to fully understand the genetic risks associated with dnTMA post-KTx.
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Complement is involved in the pathogenesis of neuroimmune disease, but the detailed pathological roles of the complement pathway remain incompletely understood. Recently, eculizumab, a humanized anti-C5 monoclonal antibody, has been clinically applied against neuroimmune diseases such as myasthenia gravis and neuromyelitis optica spectrum disorders (NMOSD). Clinical application of eculizumab is also being investigated for another neuroimmune disease, Guillain-Barré syndrome (GBS).

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In the context of the theory of multi-agent systems, the shepherding problem refers to designing the dynamics of a herding agent, called a sheepdog, so that a given flock of agents, called sheep, is guided into a goal region. Although several effective methodologies and algorithms have been proposed in the last decade for the shepherding problem under various formulations, little research has been directed to the practically important case in which the flock contains sheep agents unresponsive to the sheepdog agent. To fill in this gap, we propose a sheepdog algorithm for guiding unresponsive sheep in this paper.

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  • Transplant-associated thrombotic microangiopathy (TA-TMA) is a serious complication that can occur after hematopoietic stem cell transplantation, particularly in adults.
  • A study was conducted with 30 patients (15 with TA-TMA and 15 without) to investigate the role of genetic variants and complement proteins in the development of TA-TMA.
  • The findings revealed that high levels of the Ba protein on Day 7 post-transplant are a strong predictor of TA-TMA, while genetic variants related to complement did not significantly correlate with its development.
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Rationale: Complement deficiency are known to be predisposed to disseminated gonococcal infection (DGI). We herein present a case of DGI involving a Japanese man who latently had a complement 7 deficiency with compound heterozygous variants.

Patient Concerns: A previously healthy 51-year-old Japanese man complained of sudden-onset high fever.

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Native and recombinant collectins are purified by using mannan-agarose and an anti-collectin antibody column. The use of sandwich enzyme-linked immunosorbent assay (ELISA) with two antibodies against human mannan-binding lectin (MBL) enables elucidation of the collectin concentration in the blood, serum, and plasma. The collectin sugar specificity is demonstrated by determining the concentration of saccharide required to inhibit sugar binding by 50% in a saccharide-binding assay.

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  • The complement system was originally thought to mainly help protect against infections, but further research has revealed its involvement in various diseases.
  • Eculizumab (ECZ), an anti-C5 monoclonal antibody, was first approved in the U.S. in 2007 for treating paroxysmal nocturnal hemoglobinuria, with approvals in Japan for related conditions following in 2010 and 2013.
  • The success of ECZ has sparked interest among pharmaceutical companies to create new drugs targeting the complement system, leading to a surge in the development of complement therapeutics.
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In sepsis, systemic coagulation activation frequently causes disseminated intravascular coagulation (DIC), and the uncontrolled activation of the complement system can induce multiple organ dysfunction and poor prognosis. This study aimed to examine the association of DIC with levels of collectin kidney 1 (CL-K1), a novel collectin of the complement system, and mannose-binding lectin (MBL), a classical-type collectin in patients with sepsis. We collected blood samples prospectively from adult patients with sepsis admitted to the intensive care unit (ICU) from day 1 (admission) to day 5.

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The Industrial Internet of Things (IIoT) applications are required to provide precise measurement functions as feedback for controlling devices. The applications traditionally use polling-based communication protocols. However, in polling-based communication over current industrial wireless network protocols such as ISA100.

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Collectins are C-type lectins that are involved in innate immunity as pattern recognition molecules. Recently, collectin kidney 1 (CL-K1) has been discovered, and in vitro studies have shown that CL-K1 binds to microbes and activates the lectin complement pathway. However, in vivo functions of CL-K1 against microbes have not been elucidated.

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  • Pentraxins (PTXs) are proteins that play a role in the body's defense during illness, and recent studies show that CL-P1 and CRP affect complement activation without forming a key complex in normal conditions due to factor H's inhibitory effects.
  • * Researchers used specific cell lines to examine how CL-P1 interacts with other PTXs, leading to experiments on binding and complement deposition.
  • * The study found that CL-P1 can bind to different proteins and activate complement pathways while also preventing damage to host tissues, suggesting it may protect against overactive immune responses.
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Both the complement system and collectins play important roles in our innate immune system. The collectins, which are characterized by their inclusion of a collagen-like region and a calcium-dependent carbohydrate recognition domain, are pattern recognition molecules and include the well characterized proteins mannan-binding lectin (MBL) and the surfactant proteins SP-A/-D. Collectin liver 1 (CL-L1), collectin kidney 1 (CL-K1) and collectin placenta 1 (CL-P1) are the most recently discovered collectins.

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Background: C-reactive protein (CRP) is a plasma pentraxin family protein that is massively induced as part of the innate immune response to infection and tissue injury. CRP and other pentraxin proteins can activate a complement pathway through C1q, collectins, or on microbe surfaces. It has been found that a lectin-like oxidized LDL receptor 1 (LOX-1), which is an endothelial scavenger receptor (SR) having a C-type lectin-like domain, interacts with CRP to activate the complement pathway using C1q.

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Understanding the molecular components of immune recognition of the tuberculosis (TB) bacillus, Mycobacterium tuberculosis, can help designing novel strategies to combat TB. Here, we identify collectin CL-LK as a novel soluble C-type lectin able to bind M. tuberculosis, and characterize mycobacterial mannose-capped lipoarabinomannan as a primary ligand for CL-LK.

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Background: Collectin-K1 (CL-K1, or CL-11) is a multifunctional Ca(2+)-dependent lectin with roles in innate immunity, apoptosis and embryogenesis. It binds to carbohydrates on pathogens to activate the lectin pathway of complement and together with its associated serine protease MASP-3 serves as a guidance cue for neural crest development. High serum levels are associated with disseminated intravascular coagulation, where spontaneous clotting can lead to multiple organ failure.

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Green tea is known to have various health benefits for humans. However, the effect of green tea consumption on cognitive dysfunction remains to be clinically verified. We conducted a clinical study to investigate the effects of green tea consumption on cognitive dysfunction.

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Background: Collectins are considered to play a role in host defense via complement activation and opsonization, and are composed of a collagen-like domain and a carbohydrate recognition domain (CRD). Collectin placenta 1 (CL-P1) showed scavenger receptor activity as functions in vitro, and has three candidate domains: a coiled-coil domain, a collagen-like domain and CRD.

Methods: We constructed seven types of CL-P1 deletion mutants to determine the site of each ligand binding domain, and observed whether the specific binding to sugar ligand, microbes, or oxidized LDL decreases or not in cells with CL-P1 deletion mutants and CL-P1 containing mutations of amino acid, respectively.

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Background: Scavenger receptor CL-P1 (collectin placenta 1) has been found recently as a first membrane-type collectin which is mainly expressed in vascular endothelial cells. CL-P1 can endocytose OxLDL as well as microbes but in general, the endocytosis mechanism of a scavenger receptor is not well elucidated.

Methods: We screened a placental cDNA library using a yeast two-hybrid system to detect molecules associated with the cytoplasmic domain of CL-P1.

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Collectin kidney 1 (CL-K1) is a recently identified collectin that is synthesized in most organs and circulates in blood. CL-K1 is an innate immune molecule that may play a significant role in host defense. As some collectins also play a role in coagulation, we hypothesized that an effect of CL-K1 may be apparent in disseminated intravascular coagulation (DIC), a gross derangement of the coagulation system that occurs in the setting of profound activation of the innate immune system.

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The concept of biologically inspired networking has been introduced to tackle unpredictable and unstable situations in computer networks, especially in wireless ad hoc networks where network conditions are continuously changing, resulting in the need of robustness and adaptability of control methods. Unfortunately, existing methods often rely heavily on the detailed knowledge of each network component and the preconfigured, that is, fine-tuned, parameters. In this paper, we utilize a new concept, called attractor perturbation (AP), which enables controlling the network performance using only end-to-end information.

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  • The complement system works alongside antibodies, made up of proteins C1-C9 and regulatory molecules, to support immune functions.
  • It plays three main roles: enhancing phagocytosis to clear microbes, directly destroying bacteria through the membrane attack complex, and activating immune responses that recruit neutrophils.
  • The text also summarizes recent findings and treatments for paroxysmal nocturnal hemoglobinuria and hereditary angioedema, along with a brief discussion on the rare disorder 3MC syndrome and potential new roles of complement factors beyond innate immunity.
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