Publications by authors named "Chihiro Akazawa"

Mesenchymal stem/stromal cells (MSCs) are distributed in various tissues and are used in clinical applications as a source of transplanted cells because of their easy harvestability. Although MSCs express numerous cell-surface antigens, single-cell analyses have revealed a highly heterogeneous cell population depending on the original tissue and donor conditions, including age and interindividual differences. This heterogeneity leads to differences in their functions, such as multipotency and immunomodulatory effects, making it challenging to effectively treat targeted diseases.

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Myeloid cells, which originate from hematopoietic stem/progenitor cells (HSPCs), play a crucial role in mitigating infections. This study aimed to explore the impact of mesenchymal stem/stromal cells (MSCs) on the differentiation of HSPCs and progenitors through the C-C motif chemokine CCL2/CCR2 signaling pathway. Murine MSCs, identified as PDGFRαSca-1 cells (PαS cells), were found to secrete CCL2, particularly in response to lipopolysaccharide stimulation.

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  • * In this research, the focus was on the CD29+ cell population in bovine muscle, which shows heterogeneity and contains promising subpopulations for cultured meat production.
  • * Specific CD29+ cell types were identified: CD29+CD44-CD344- cells had high adipogenic potential for long-term culture, while CD29+CD44+ cells proliferated quickly but weren't sustainable, enhancing understanding for more effective cultured meat production.
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Purpose: It has long been established that the failure of enteric neural crest cells (ENCCs) to colonize the entire gut results in aganglionosis at the distal colon in Hirschsprung disease (HD). However, it is still unclear how the intestinal microenvironment of the distal aganglionic gut differs from that of the proximal ganglionic gut in HD versus normal gut. We have recently succeeded in transplanting ENCC into aganglionic gut in endothelin receptor B (Ednrb) knockout (KO) mice.

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Purpose: Intestinal neuronal dysplasia (IND) is a congenital anomaly affecting gastrointestinal neural innervation, but the pathogenesis remains unclear. The homozygous Ncx/Hox11L.1 knockout (Ncx) mice exhibit megacolon and enteric ganglia anomalies, resembling IND phenotypes.

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Adipose stem and progenitor cells (ASPCs) have been isolated from humans and animals for use in regenerative medicine and therapy. However, knowledge of ASPCs in other species is limited. Particularly, ASPCs in livestock are expected to enhance the fat content and meat composition.

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The incidence of inflammatory bowel diseases (IBD) is increasing worldwide. Mesenchymal stem/stromal cells (MSCs) have immunomodulatory functions and are a promising source for cell transplantation therapy for IBD. However, owing to their heterogeneous nature, their therapeutic efficacy in colitis is controversial and depends on the delivery route and form of transplanted cells.

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  • - Schwartz-Jampel syndrome (SJS) is an autosomal recessive disorder caused by mutations in the gene that encodes perlecan, a key basement membrane protein, which leads to symptoms like myotonia—a muscle stiffness condition.
  • - Diagnosing myotonia, especially in neonates and young children, is challenging since it's primarily based on physical examination, and there's limited understanding of how it develops in SJS.
  • - Researchers created a cellular model of SJS using patient-derived stem cells, which showed heightened reactions to acetylcholine, helping to confirm the model's relevance for studying SJS and potentially aiding in the search for effective treatments.
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Bone is one of the largest organ systems in humans and is considered to regulate whole-body homeostasis in cooperation with other organs. We have previously reported that a sympathetic or sensory nervous system inside bone regulates bone homeostasis. However, the detailed regulatory mechanism, including the distribution of nerves inside bone, remains unknown.

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  • This study investigates how enteric neural crest-derived cells (ENCCs) behave when transplanted into the aganglionic gut of two mouse models: endothelin receptor B knockout (Ednrb-KO) mice and wild-type (WT) mice.
  • Researchers isolated ENCCs from fetal Sox10 transgenic mice and tracked their migration and differentiation after transplantation, finding that ENCCs successfully migrated into the myenteric region of both mouse types and showed significant neuronal differentiation in Ednrb-KO mice.
  • The findings suggest that the microenvironment in the aganglionic gut influences ENCC behavior, particularly enhancing neuronal differentiation in Ednrb-KO mice compared to their
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Purpose: Failure of enteric neural crest-derived cells (ENCCs) to correctly colonize the embryonic gut results in Hirschsprung's disease (HD). Embryonic stem cells (ESCs) have the potential to differentiate into all tissue-specific cells and lineages, including ENCCs. We investigated the cellular differentiation of ESCs from Sox10-Venus mice into both control and endothelin receptor-B knockout (Ednrb KO) mouse gut to assess each region.

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  • Understanding the immune response and sustained activation after COVID-19 infection and vaccination is key for developing preventive and therapeutic measures.
  • A study evaluated serum cytokine levels and their relationship with neutralizing antibody levels in vaccinated and recovered individuals, discovering unique patterns in response to different SARS-CoV-2 variants.
  • Key biomarkers like IL-10 and CCL2 were identified, suggesting that personalized therapeutic strategies should be considered based on individual immune responses and vaccination history.
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  • Hematopoietic stem/progenitor cells (HSCs) rely on interactions with mesenchymal stem/stromal cells (MSCs) to maintain their self-renewal and multipotency, which are crucial for medical applications.
  • Culturing MSCs to increase their numbers leads to a loss of important stem cell traits, including their ability to differentiate and proliferate effectively.
  • The study reveals that the c-Mpl signaling pathway is vital for HSC maintenance and enhances MSC proliferation; without this signaling, both HSC functionality and MSC stem cell markers are diminished.
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Purpose: Cell therapy is a promising approach to treat enteric neuropathies such as Hirschsprung disease (HD). Recent studies have reported that enteric neurons derived from stem cells (ENCCs) can be grafted into the HD colon. Thus, we investigated the migration and generation of enteric neurospheres from SOX10-VENUS mice after transplantation into control or Ednrb KO mice, which are a model of HD.

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Background: Previous research indicates that patients with mild cognitive impairment (MCI) are more likely to have poor oral health and impairments in oral functions, which may be due to few remaining teeth and impaired tongue and lip motor function. However, the oral health of those patients following comprehensive cognitive assessment by a dementia specialist has not been sufficiently investigated. Therefore, this study aimed to clarify the oral function of patients with MCI and the association between oral health and lower cognitive function.

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Manipulating lymphocyte functions with gene silencing approaches is promising for treating autoimmunity, inflammation, and cancer. Although oligonucleotide therapy has been proven to be successful in treating several conditions, efficient in vivo delivery of oligonucleotide to lymphocyte populations remains a challenge. Here, we demonstrate that intravenous injection of a heteroduplex oligonucleotide (HDO), comprised of an antisense oligonucleotide (ASO) and its complementary RNA conjugated to α-tocopherol, silences lymphocyte endogenous gene expression with higher potency, efficacy, and longer retention time than ASOs.

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The current process of meat production using livestock has significant effects on the global environment, including high emissions of greenhouse gases. In recent years, cultured meat has attracted attention as a way to acquire animal proteins. However, the lack of markers that isolate proliferating cells from bovine tissues and the complex structure of the meat make it difficult to culture meat in a dish.

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Mesenchymal stem/stromal cells (MSCs) are present in various body tissues and help in maintaining homeostasis. The stemness of MSCs has been evaluated . In addition, analyses of cell surface antigens and gene expression patterns have shown that MSCs comprise a heterogeneous population, and the diverse and complex nature of MSCs makes it difficult to identify the specific roles in diseases.

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Junctional adhesion molecules (JAMs) are expressed in diverse types of stem and progenitor cells, but their physiological significance has yet to be established. Here, we report that JAMs exhibit a novel mode of interaction and biological activity in adipose-derived stromal/stem cells (ADSCs). Among the JAM family members, JAM-B and JAM-C were concentrated along the cell membranes of mouse ADSCs.

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We examined the usefulness of five COVID-19 antibody detection tests using 114 serum samples at various time points from 34 Japanese COVID-19 patients. We examined Elecsys Anti-SARS-CoV-2 from Roche, and four immunochromatography tests from Hangzhou Laihe Biotech, Artron Laboratories, Chil, and Nadal. In the first week after onset, Elecsys had 40% positivity in Group S (severe cases) but was negative in Group M (mild-moderate cases).

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Human mesenchymal stem/stromal cells (hMSCs) have garnered enormous interest as a potential resource for cell-based therapies. However, the molecular mechanisms regulating senescence in hMSCs remain unclear. To elucidate these mechanisms, we performed gene expression profiling to compare clonal immature MSCs exhibiting multipotency with less potent MSCs.

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Somatic stem cells have been isolated from multiple human tissues for their potential usefulness in cell therapy. Currently, mesenchymal stromal cells (MSCs) are prepared after several passages requiring a few months of cell culture. In this study, we used a prospective isolation method of somatic stem cells from gestational or fat tissues, which were identified using CD73 antibody.

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In the spinal cord, the axonal tracts with various caliber sizes are myelinated by oligodendrocytes and function as high-velocity ways for motor and sensory nerve signals. In some neurological disorders, such as multiple sclerosis, demyelination of small caliber axons is observed in the spinal cord. While type I/II oligodendrocytes among the four types are known to myelinate small diameter axons, their characteristics including identification of regulating molecules have not been understood yet.

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Transcriptional co-activator with PDZ-binding motif (TAZ) plays versatile roles in the regulation of cell proliferation and differentiation. TAZ activity changes in response to the cellular environment such as mechanic and nutritional stimuli, osmolarity, and hypoxia. To understand the physiological roles of TAZ, chemical compounds that activate TAZ in cells are useful as experimental reagents.

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In the developing central nervous system (CNS), oligodendrocyte precursor cells (OPCs) migrate along blood vessels and are widely distributed in the CNS. Meanwhile, OPCs require survival factors from the extracellular microenvironment. In other tissues, laminins, heterotrimetric (αβγ) extracellular matrix proteins, promote cell migration and survival.

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