Articles tagged with Stem Cell Research
A Penn State research team has discovered a compound produced from fish oil that targets and kills leukemia stem cells, potentially leading to a cure for the disease. The compound, D12-PGJ3, selectively activates a gene in leukemia stem cells that programs their own death.
A study found that a combined immunosuppressive regimen improved the survival of human spinal stem cells in ALS rats. The results suggest that this treatment approach may be a potential therapy for ALS, a degenerative neurological disease.
A new approach using an HIV drug has significantly reduced the incidence of graft-versus-host disease (GvHD) in blood cancer patients after allogeneic stem cell transplantation. Maraviroc dramatically reduced GvHD in organs such as the gut and liver without compromising the immune system.
Researchers found that patients receiving bone marrow transplants from unrelated donors had the same survival rates as those receiving blood stem cell transplants. However, PBSCs resulted in better engraftment but higher rates of chronic graft-versus-host disease (GVHD), a serious post-transplant complication.
A survey of US human embryonic stem cell researchers found nearly four in ten faced excessive delay acquiring a line, while over one-quarter were unable to get the line they needed. The main reasons for these issues include material transfer agreements, research approval, and federal policies.
Researchers at King's College London have made a breakthrough in developing xeno-free human embryonic stem cell lines that are suitable for public benefit. The lines will be grown and processed by the UKSCB to provide stem cell stocks for clinical research and treatment.
Researchers in Canada have developed a technique to produce large quantities of endoderm cells from human pluripotent stem cells, overcoming a key hurdle in regenerative medicine. The method allows for significant increases in effective cell production, enabling the potential for regenerative treatments for diabetes and liver disease.
Researchers found that ephrin proteins help satellite cells navigate and differentiate into muscle fibers. By understanding this process, they hope to develop more effective treatments for muscular dystrophy, a condition where muscles are easily damaged and patients' satellite cells lose their ability to repair.
Researchers found that newly derived human embryonic stem cell lines have a better molecular signature than established lines, indicating higher quality and potentially better performance in disease modeling. The study suggests that maintaining the original state of X chromosome inactivation could be crucial for achieving optimal results.
Researchers from UCLA's cancer and stem cell centers have successfully engineered blood stem cells to create cancer-killing T-cells that seek out and attack human melanoma. The approach could lead to a sustained immune response, potentially protecting against cancer recurrence.
The researchers have developed a highly efficient system to generate nucleic acid molecules, called aptamers, for next-generation disease diagnosis and testing. The Quantitative Parallel Aptamer Selection System (QPASS) aims to make devices like instant diagnosis machines ready for widespread clinical use.
A collaborative study from the International Stem Cell Initiative analyzed human pluripotent stem cells' genetic stability and found that 75% remained normal after prolonged culture. However, researchers detected genetic changes similar to those seen in human cancers, highlighting the need for detecting and eliminating abnormal cells.
Researchers studied hematopoietic stem cells in healthy young and elderly individuals, finding that older stem cells produce fewer lymphocytes and more myeloid cells. This bias may lead to inadequate immune responses and increased risk of blood cancers.
Researchers identified a portion of the genome mutated during long-term culture of human embryonic stem cells, which may compromise their utility for regenerative medicine. The study highlights the importance of understanding genetic changes in hESCs and their potential impact on cell therapy applications.
Scientists at the University of Bonn have made a breakthrough in understanding Machado-Joseph disease by studying nerve cells derived from patients' skin cells. The research reveals that electrical activity in these cells triggers protein aggregation, explaining why the disease affects only nerve cells.
Researchers have found that B-type lamins are necessary for proper organ development, but not for the replication and differentiation of embryonic stem cells. Mice deficient in B-type lamins were born with developmental defects, highlighting the protein's importance in tissue organization.
Researchers have discovered a new muscle repair gene, MEGF10, which plays a crucial role in the fusion process of satellite cells. The findings provide accurate genetic testing and diagnosis for devastating conditions affecting muscle function, enabling hope for families affected by progressive muscle disease.
Researchers found that pluripotent stem cells respire at the same level as differentiated body cells but produce very little energy. UCP2 protein blocks respiration substrates from entering mitochondria, allowing glycolysis to dominate. The study suggests that changes in metabolism drive cell differentiation.
Researchers at Mount Sinai School of Medicine discovered fetal stem cells in the placenta can migrate to and repair damaged maternal hearts after a heart attack. The study found that these cells reprogram into beating heart cells, providing a potential therapeutic agent for cardiac regeneration.
Researchers used adult stem cells to treat patients with heart failure after a myocardial infarction. The trial showed an average improvement of 12% in left ventricular ejection fraction (LVEF) and a decrease in scarred regions, suggesting that heart tissue can regenerate.
A Mayo Clinic study found that stem cells delivered two to three weeks after a heart attack do not improve heart function. The research provides vital information for the field of cell therapy and cautions against seeking stem cell treatment outside the US.
Researchers from the Chinese University of Hong Kong have developed a technique to reprogram stem cells into a more primitive state, increasing their survival rates and therapeutic efficacy. This breakthrough could lead to improved treatment outcomes for conditions such as degenerative diseases and blood supply disorders.
Researchers at the University of Texas Health Science Center have discovered that old stem cells can be rejuvenated by being placed in a young microenvironment. This could lead to personal stem cell banks treating age-related diseases, with the potential for regular rescue and infusion.
A new study reveals that adult stem cells can reshape organs in response to changes, with implications for diabetes and obesity. Intestinal stem cells respond to increased food intake by producing more cells, expanding the gut's size.
Researchers at A*STAR's Genome Institute of Singapore and Institute of Molecular Biology identify distal airway stem cells as the key to forming new alveoli, paving the way for novel therapies for respiratory diseases. The discovery provides insight into genes and secreted factors that can be used to enhance lung regeneration.
Researchers have cloned human airway stem cells, which can form alveoli tissue and rapidly deploy in lung regeneration. The findings suggest new strategies for enhancing lung regeneration following damage from infection or chronic disease.
Treatment with high-dose melphalan and autologous stem cell transplantation achieved a high organ response rate and increased overall survival, even in patients without hematologic complete response. The study found that careful patient selection and experienced management can lead to low treatment-related mortality rates.
Rutgers University has established a stem cell repository to study mental health disorders such as autism and schizophrenia. The repository will provide researchers with induced pluripotent stem cells derived from individuals with these conditions, enabling them to better understand the causes of mental disorders.
Researchers believe that timing has finally come to support the conduct of human clinical trials for stem cell therapy in spinal cord injuries. Currently, research is largely stuck at the animal model stage. Studies evaluate 11 different cell types/sources and provide evidence justifying their use.
Researchers have successfully joined epidermic stem cells to create healthy skin in the lab, preserving their regenerative potential. They can now use these cells to regenerate patients' skin, offering a new therapeutic strategy for those with limited treatment options.
Researchers have developed a method to grow cardiac muscle cells from human cord blood stem cells, which could lead to new treatment options for patients with damaged hearts. The study found that these cells can be expanded and differentiated into cardiomyocyte-like cells, overcoming the technical hurdle of deriving cardiac muscle-type...
Scientists have cleanly corrected a human gene mutation in a patient's stem cells, using cutting-edge methods to target and correct the sequence of the genome. The corrected gene worked normally, demonstrating the potential for patient-specific therapies.
A young scientist has won a $10,000 award for her research on regenerating eyes using stem cells from hair follicles. Her study showed an 80% rate of differentiation in mouse eyes following a cell transplant, highlighting the promising therapeutic potential of these cells.
Professor Peter J. Coffey's pioneering stem cell research aims to replace damaged retinal pigment epithelium cells in Age-Related Macular Degeneration. Clinical trials using his therapy are expected to begin in 2012, offering hope for preventing blindness and restoring sight.
Researchers developed a new method for reprogramming human cells into stem cells, increasing efficiency by 100-fold and producing high-quality cells faster. This breakthrough has potential applications in medicine, such as organ replacement, bone replacement, and treatment of neurodegenerative diseases.
Researchers have discovered a method to harness patient-derived neural stem cells as an alternative source of insulin-producing beta cells for regenerative treatments. This breakthrough could potentially overcome the shortage of donor pancreatic beta cells and provide a safer, more accessible way to treat diabetes.
Lack of compensation for human egg donors could stall recent breakthroughs in stem cell research due to difficulty in recruiting altruistic donors. A recent study on somatic cell nuclear transfer (SCNT) has created the first human stem cell line, but more donor eggs are needed to advance research.
Dr. Malgorzata Borowiak has been awarded a grant from the Helmholtz Association to return to the Max Delbrück Center for Molecular Medicine (MDC) Berlin-Buch, Germany, as head of a Young Investigators Group. She aims to contribute to diabetes research by studying beta cell development.
Researchers identified a new pathway of stem cell activity in the subventricular zone of the human brain, which targets the prefrontal cortex in newborns. This discovery challenges previous reports that suggested neural stem cells remain active into adulthood.
Scientists at Johns Hopkins Medicine have corrected the genetic alteration causing sickle cell disease by using a patient's own stem cells. The team found four working iPS cell lines containing correct copies of the hemoglobin gene and successfully converted them into immature red blood cells.
Researchers successfully grafted deciduous canine teeth and dental pulp stem cells into parent canines, demonstrating bone regeneration after four weeks. The study found increased immunosuppressive activity of these stem cells, paving the way for potential clinical applications in allogenic in vivo stem cell transplantation.
A study from UNC Chapel Hill School of Medicine has illuminated a critical step in demethylation, giving stem cell researchers information to reprogram adult cells. The disappearance of chemical tags is a passive process, not catalyzed by an enzyme.
Researchers at Tel Aviv University have developed a patented technology that uses bone marrow stem cells to produce neuroprotectors, proteins that shield the brain from neurodegenerative disorders. The treatment has shown efficacy in animal models and is now being tested in human clinical trials.
Scientists have found a control switch that regulates stem cell pluripotency by altering the DNA binding properties of FOXP1, facilitating maintenance of pluripotency and reprogramming adult cells. The discovery has significant implications for therapeutic applications in regenerative medicine and cancer research.
Researchers at Yale University have successfully converted uterine stem cells into insulin-producing cells, which could lead to the development of a new treatment for Type 1 diabetes. The study found that these stem cells can adopt the characteristics of beta cells in the pancreas and produce insulin in response to glucose.
A team of researchers evaluated the effect of low-power Terahertz radiation on mouse stem cells, finding temperature increases were minimal and heat shock protein expression was unaffected. However, certain genes showed clear effects from THz irradiation, suggesting further investigations are needed to generalize findings.
Researchers at University of Wisconsin-Madison report 99% protein similarity between two types of do-it-all stem cells, shedding light on their potential applications in cell replacement therapies. The study measured over 6,000 proteins using mass spectrometry and provides insights into their biological role.
Patients in another clinical trial have reached the two-year mark following infusion of processed adult stem cells, while a new $12.8 million NIH grant renewal aims to perfect cardiac stem cell therapy for heart regeneration after a heart attack.
A Scripps Research team has overcome a major purification problem for stem cells, enabling more reliable and safe treatments. The new method uses lectin arrays to separate stem cells from other cell types, promising significant cost savings and reliability improvements.
Researchers identified a protein that helps maintain mouse stem cell pluripotency by activating signal pathways via CC chemokine ligand 2 (CCL2). This finding offers insights into cultivating human iPS/ES cells without feeder cells, reducing the risk of contamination and health risks.
Researchers at IRB Barcelona have identified human colon stem cells and developed a method to grow them in lab-plates. This breakthrough could lead to significant advances in regenerative medicine, potentially treating diseases such as colorectal cancer and Crohn's disease.
Researchers at Scripps Research Institute have successfully produced stem cells from two endangered species, a drill and the northern white rhinoceros. These cells could enable lifesaving medical therapies or offer the potential to preserve or expand genetic diversity by offering new reproduction possibilities.
Research led by McMaster University found that exercise triggers mesenchymal stem cells to become bone instead of fat, leading to improved blood production and overall health. This finding suggests a new potential for exercise as a non-medicinal treatment for blood-related disorders.
Yale scientists identify adipose precursor cells as key players in triggering hair growth. These cells produce PDGF molecules necessary for producing hair growth in mice. The study offers a promising avenue for developing new treatments for male pattern baldness by targeting these stem cells and signals.
Researchers at UTHealth report using a patient's own bone marrow stem cells as a safe and feasible treatment for acute stroke. The study, published in Annals of Neurology, showed no severe adverse events among the 10 patients enrolled.
Scientists describe an advance in encouraging stem cells to make decisions about their fate using chemically defined surfaces. This technology holds promise for regenerative medicine, including growing organs for transplants and tissues for treating diseases.
Scientists discover large RNAs regulate embryonic development by physically interacting with proteins, suggesting a critical role in developmental decisions. The study reveals that lincRNAs may play similar roles in most cells and could be engineered to target key genes in disease.
Researchers have found that acute myeloid leukemia (AML) contains rare cancer stem cells (LSCs) with unique properties that can predict clinical outcome. The LSC signature can identify patients who may benefit from more aggressive therapy, enabling personalized treatment approaches.
Researchers have discovered that human amniotic fluid-derived stem cells (hAECs) can differentiate into various cell types, including those found in the lungs. Transplanted hAECs were shown to reduce pulmonary fibrosis and enhance lung regeneration in animal models of lung disease.
Researchers at Tel Aviv University have discovered that oral mucosa stem cells can be manipulated into fetal-like stem cells with high therapeutic potential for treating neurodegenerative, heart, and autoimmune diseases. The cells can be derived from a small biopsy of tissue and show minimal discomfort and healing time.