Articles tagged with Stem Cell Research
A small molecule drug improved the fitness of hematopoietic stem cells used in cell transplants, potentially enhancing the success of procedures like ex vivo gene therapy. The study found that targeting extracellular vesicles relieved stress on cells outside the body, improving their performance when transplanted back in.
A new biomimetic chip has been developed to simulate the human gastric mucosa, combining organoid and organ-on-a-chip technologies. The biochip replicates mechanical stimulation and cell-to-cell interactions, mimicking key features of the human stomach's defense mechanisms.
A study found that autologous haematopoietic stem cell transplantation (aHSCT) can safely slow the progression of relapsing-remitting multiple sclerosis. In nearly two-thirds of patients, there was no evidence of disease activity after 5 years and almost two-thirds after 10 years.
Scientists have identified a specific process that helps control transposable elements, which destabilize the genetic code and contribute to aging. Strengthening this pathway in Caenorhabditis elegans extended its lifespan.
Scientists have identified thousands of non-coding genetic variants linked to Alzheimer's disease, focusing on their impact on microglial gene expression and function. The study found that turning off specific regions can affect multiple genes, highlighting the complex mechanisms underlying AD.
Researchers compared transcriptomic profiles of human 8-cell-like cells and blastomeres to understand early human embryonic development. The study found that reprogrammed iBM cells showed the highest similarity to the 8-cell-stage embryo, while other 8CLCs were heterogeneous.
A recent study by Boston Medical Center and Boston University's Center for Regenerative Medicine discovered that hemogenic endothelial cells in the fetal lung contribute to blood cell formation. This breakthrough expands our understanding of blood development and its relationship with overall health.
A new type of bone-forming stem cell, DDR2+, has been found to cause premature skull fusion in infants. The researchers discovered that the abnormal proliferation of this stem cell leads to an excess of bone-making cells, resulting in craniosynostosis.
The NIH award will explore how damage to mitochondria affects bioenergetic function and organ function, leading to disease severity and failure. The study aims to better understand mitochondria mutations and develop new therapies for patients with mitochondrial disorders.
Researchers at the University of Cambridge have made a groundbreaking discovery that could lead to more effective treatments for neuroblastoma, a devastating form of childhood cancer. The new approach uses a combination of two drugs to encourage cancer cells to become normal non-dividing cells, potentially reducing side effects.
The NY Genome Center will use patient-derived stem cells models combined with functional genomics and genome engineering to shed light on the biological processes underlying bipolar disorder. The study aims to address gaps in knowledge of genetic risk for bipolar disorder and advance treatment strategies.
Dr. Hung Nguyen is studying how medium chain fatty acid foods like coconut oil and avocados affect GVHD severity and mortality in transplant patients. His goal is to develop a dietary approach that reduces inflammation and corticosteroid use, improving patient outcomes for blood cancers.
Researchers have discovered that embryonic stem cells are guided by a complex interplay of signaling molecules to determine their cell type. The study found that fibroblast growth factor (FGF) acts as an antagonist of the signal molecule BMP, influencing cell differentiation and fate.
Researchers have designed an implantable device that carries hundreds of thousands of insulin-producing islet cells and has its own on-board oxygen factory, generating oxygen by splitting water vapor. The device was tested in diabetic mice and maintained normal blood glucose levels for at least a month.
A systematic review and meta-analysis of 195 clinical trials found that cell therapy can reduce the risk of death from COVID-19 by 60%. The studies, conducted in 30 countries between January 2020 and December 2021, used various types of cells, including mesenchymal stem cells and natural killer cells.
The International Society for Stem Cell Research (ISSCR) has introduced a 'checklist' to promote global best practices for human stem cell research. The checklist aims to increase transparency and clarity in the reporting of key quality control measures, enabling authors to disclose critical experimental details.
Researchers developed a technique called CHOOSE that allows them to test the effect of multiple mutations in parallel and at a single-cell level within human brain organoids. The study identified critical transcriptional changes regulated through common networks, or GRNs, and found that some cell types are more susceptible to autism mu...
Researchers at Weill Cornell Medicine discovered a distinct type of stem cell that secretes protein MFGE8, favoring tumor metastases to the spine. This finding helps explain why solid tumors often spread to the spine and could lead to new orthopedic and cancer treatments.
A preclinical study suggests that nanowired cardiac organoids could repair hearts instead of just preventing further damage. The treatment, led by Dr. Mei and Ryan Barrs, showed a 69% increase in heart function, promising a new therapy for heart disease.
Researchers found that enteroendocrine cells in Drosophila intestinal epithelium undergo dedifferentiation into intestinal stem cells in response to nutritional changes, such as recovery from starvation. This process is vital for ISC expansion and subsequent intestinal growth following food intake.
A phase I clinical trial shows that transplanting P63+ lung progenitor cells can repair damaged lung tissue in patients with chronic obstructive pulmonary disease (COPD), improving breathing and quality of life. The treatment increased lung function, reduced symptoms, and even repaired mild emphysema in some patients.
Researchers have developed a new method to study the inner workings of cell nuclei during embryonic stem cell differentiation. By using fluorescent proteins, they found that biomaterials become more uniformly distributed as cells mature, resembling oil droplets in water, but with intriguing complexities.
Scientists have created chimeric embryos containing a combination of human and pig cells, which developed into structurally normal kidneys with 50-60% human cells. The researchers successfully grew humanized organs inside pigs, offering new possibilities for studying human development and developmental diseases.
A USC Stem Cell-led mouse study reveals that lowering testosterone can improve the resilience of male kidneys by reducing their vulnerability to disease. The researchers also found that three months of calorie restriction has a similar effect, suggesting new potential treatments for kidney diseases.
A groundbreaking study from the University of Copenhagen sheds light on the significance of transmitting epigenetic information during cell division for proper function of embryonic stem cells. The researchers found that histones play a crucial role in maintaining epigenome stability and cell identity.
Researchers at Prolacta and MD Anderson Cancer Center found a human milk-based synbiotic to safely control the gut microbiome in adults, opening the door to precision microbiome engineering. The study demonstrates significant precision in modulating adult gut microbiomes.
Researchers have developed a human milk-based synbiotic that safely modulates damaged adult gut microbiomes. The study found that this symbiotic reshapes gut microbial composition and metabolites, offering new possibilities for treating dysbiotic conditions.
Researchers developed a new formulation of doxorubicin that targets cancer cells while reducing cardiotoxicity. The protein-shell encapsulation increases specificity for cancer cells and decreases harm to healthy heart cells.
For the first time, researchers have identified self-renewing stem cells in the human thymus, which could lead to new treatments for immune diseases and cancer. The thymus, a gland located in the chest, was previously thought not to contain epithelial stem cells.
A new molecule called A11 has been found to reduce inflammation and improve memory in models of Alzheimer's disease. By targeting the genetic transcription factor PU.1, A11 suppresses inflammatory gene expression in microglia immune cells, leading to reduced neurodegeneration and improved cognition.
Researchers have developed a new way to sort cells by type using light-based stimulated Raman spectroscopy, offering a label-free and nondestructive approach for various biomedical applications. The technique enables the separation of cells based on their intracellular chemical composition in high-throughput manner.
A CRISPR-Cas3 system has restored dystrophin protein function in induced pluripotent stem cells from patients with Duchenne muscular dystrophy. The approach uses a dual CRISPR RNA method to remove large sections of the dystrophin gene, yielding truncated but still functional proteins for various mutation patterns.
A new immune-infiltrated human kidney organoid-on-chip model enables the assessment of on-target, off-tumor effects of immunotherapeutic T cell bispecific antibody drugs. The study's findings provide important insights into which cells are targeted by a given TCB and what, if any, off-target damage arises.
Researchers at Mass General Brigham used stem cells from patients with Alzheimer's disease to study the impact of SORL1 gene damage. They found that loss of normal SORL1 function leads to a reduction in key AD proteins APOE and CLU, highlighting a potential new strategy for treatment.
A new study by Weill Cornell Medicine researchers found that severe COVID-19 infection can alter the immune system's response, causing long-lasting changes to gene expression in immune system stem cells. This can lead to symptoms of prolonged inflammation and 'long COVID' in affected individuals.
Researchers found that C9ORF72 mutations impair neural stem cell renewal, leading to reduced brain regions during embryonic development. This impairment could contribute to disease symptoms later in life. The study used patient-derived nerve cells and laboratory mice to demonstrate the impact of C9ORF72 on neurodevelopment.
A group of biologists and ethicists suggest adding clarity to ongoing research using embryo models to refine the legal definition of human embryos. They propose a new definition that focuses on what an embryo can become rather than how it came to be, allowing for improved evaluation of models and potential future recognition as embryos.
Researchers from the Wellcome Sanger Institute mapped the multiple organ functions of the human yolk sac, revealing its role in producing key hormones and blood cells. The study provides novel insights into the earliest stages of immune cell development and has implications for understanding childhood diseases.
Researchers have found that mouse stem cells mimic their parent animals' cold resistance, generating energy differently at low temperatures. This discovery opens up new avenues for studying organ preservation and human hibernation using in vitro models.
Researchers at Monash University have created a new method to reprogram human cells, called transient-naive-treatment (TNT) reprogramming, which reduces the differences between induced pluripotent stem (iPS) cells and embryonic stem cells. This breakthrough has significant implications for biomedical and therapeutic uses.
A Northwestern University study reveals how the NEK1 gene mutation affects neurons, causing instability in microtubules and disrupting nuclear import. This discovery suggests anti-cancer drugs could be used to treat ALS by stabilizing microtubules.
Researchers developed a new technique, GoT-Splice, to analyze RNA splicing in individual cells, revealing how mutations in genes controlling this process lead to diseases. The study linked these mutations to specific changes in immature red blood cells and discovered disruptions in the gene BAX.
Researchers found that epigenetic silencing shuts off key genes required for sensory cell conversion. Enzyme TET can remove methyl groups to reverse gene silencing and restore hearing capability. Progenitor cells in deaf ears may already be primed to convert into sensory hearing cells.
Researchers successfully created stem-cell derived organoids from human stem cells that secrete three essential enamel proteins. These proteins form a matrix that undergoes mineralization to create a hardened enamel structure. The breakthrough offers hope for developing novel treatments to repair and regenerate teeth.
A study published in Blood journal found that children with diverse gut microbiota before stem cell transplant had significantly better overall patient survival and fewer complications. Higher microbiota diversity was also associated with lower risk of acute graft-versus-host disease.
A team of researchers from Keck School of Medicine of USC identified key cells involved in lizard cartilage regeneration and discovered their role in rebuilding cartilage damaged by osteoarthritis. They successfully induced cartilage building in a lizard limb by recreating a tail-like signaling environment.
Researchers found that children with autism and macrocephaly exhibit excessive growth of excitatory neurons, while others show a deficit. The study's findings could help doctors diagnose autism and identify potential treatments for specific cases.
Researchers used AI to accurately classify four subtypes of Parkinson's disease from patient-derived stem cells, with one subtype reaching an accuracy of 95%. The study suggests that personalized medicine and targeted drug discovery could be possible using this approach.
Researchers at Beth Israel Deaconess Medical Center discovered a non-ectodermal and mesodermal origin for large numbers of enteric neurons born after birth. This finding overturns decades of scientific dogma and offers hope for disease-modifying cures to aging patients.
Yale researchers have created a functional humanized liver in living mice, enabling scientists to study human-specific mechanisms for regulating cholesterol levels and treating chronic liver diseases. The discovery uses progenitor stem cells and mature cells from a human liver to mimic the cellular functions of a healthy human liver.
A new approach to immunotherapy has shown long-term survival rates exceeding 50% in children with high-risk neuroblastoma. Stem cell transplantation from a parent provides a renewed immune system that responds better to immunotherapies, improving outcomes.
A study by Prof. WANG Lei and WANG Chih-chen’s group at the Institute of Biophysics (IBP) of the Chinese Academy of Sciences (CAS) establishes the relationship between oxidative protein folding and stem cell aging for the first time.
Researchers at Duke University Medical Center have identified a fatty molecule in breast milk that triggers a process in which stem cells produce new white matter, reversing neurological damage. This finding holds promise for developing therapies to treat preterm babies with cerebral palsy.
Researchers identified Tppp3+ tendon progenitor cells that actively participated in the formation of ectopic bone in vivo. These cells possess primitive progenitor properties and may regulate heterotopic ossification by releasing soluble molecules promoting osteogenic differentiation.
Scientists have identified the mechanisms behind how SOX9, a pioneer factor, reprograms adult epidermal stem cells to form cancerous tissues. By activating SOX9, researchers can induce basal cell carcinoma-like structures and study the underlying epigenetic processes.
Scientists from the University of Copenhagen found that cancer cells have different ribosomes compared to other cells, which produce specific proteins. This discovery may lead to improved treatments in regenerative medicine and potentially better treatments for cancer.
Scientists have developed an innovative method to create 'peri-gastruloids,' human embryo-like structures with extraembryonic tissues, including yolk sac and placenta. This breakthrough allows researchers to study early human development stages, mimicking the formation of vital organs.
Researchers at the Medical University of South Carolina have identified a novel class of compounds that effectively lower cholesterol, triglycerides and apoB in human liver-like cells. These molecules work independently of the LDLR pathway and offer a new treatment regimen for patients with familial hypercholesterolemia.
Researchers at Linköping University found that Wnt signalling can have varying effects on cells depending on the signal duration and receiving cell type. This discovery sheds light on how cells determine their identity, revealing a new type of cell behavior related to genome instructions.
Gang Bao's lab receives a 4-year, $2.6 million grant from the National Institutes of Health to investigate the safety and efficacy of using gene editing treatments like CRISPR-Cas9 to treat sickle cell disease. The team aims to understand the mechanisms behind large gene modifications and their biological consequences.