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Abstract: Presenting a cutting-edge discovery on the mechanisms by which immune cells influence health and disease at the later stages of cerebral ischemic stroke

Here, Chuan Qin & team use complementary models in experimental ischemic stroke, showing early post-stroke stages in which microglia recruit B cells into ischemic lesions through MIF/CD74/CXCR4, while later stage post-stroke effects involve interferon signaling in B cells that drives neuroinflammation and brain injury:

The image shows B lymphocytes (Green) in mouse dura tissue colocalizing with CD31+ blood vessels (Red).


1Department of Neurology, Tongji Hospital, Tongji Medical College and State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases;

2Key Laboratory of Vascular Aging, Ministry of Education, Tongji Hospital of Tongji Medical College; and.

3Hubei Key Laboratory of Neural Injury and Functional Reconstruction, Huazhong University of Science and Technology, Wuhan, Hubei, China.

Basal progenitors as drivers of neocortical expansion

Neocortical expansion driven by basal progenitors.

The emergence of indirect neurogenesis, driven by highly proliferative basal progenitors, contributed to the significant enlargement of the mammalian neocortex during brain evolution.

In recent years, several human-specific genes and enhancers have been described that differentially affect the biology of progenitor cells and potentially contribute to the increased neocortical complexity and disease-susceptibility of the human brain.

Emerging research is uncovering multiple pathways that disrupt basal progenitor biology, emphasizing these pathways’ involvement not only in classical neurogenesis-related disorders such as microcephaly but also in neurodevelopmental conditions traditionally linked to impairments in neuronal connectivity. sciencenewshighlights ScienceMission https://sciencemission.com/Basal-progenitors


The diversification and expansion of distinct progenitor cell subtypes during embryogenesis are essential to form the sophisticated brain structures present in vertebrates. In particular, the emergence of highly proliferative basal progenitors contributed to the evolutionary enlargement of the mammalian neocortex. Basal progenitors are at the center of indirect neurogenesis and can be divided into two main subtypes: the classical TBR2-positive intermediate progenitor cells and the outer radial glial cells, which are especially abundant in gyrencephalic species. While the function of some transcriptomic regulators is conserved across the mammalian clade, recent studies have identified human-specific genes and enhancers that uniquely affect progenitor biology, possibly driving the increased neocortical complexity and disease-susceptibility of the human brain.

Neuroimaging Biomarkers of Disease Progression and Cognitive Change in Patients With Retinal Vasculopathy With Cerebral Leukoencephalopathy

The official journal of the Guarantors of Brain. Provides researchers and clinicians with original contributions in neurology by publishing a wide range of original studies in neurological science, in addition to practical clinical articles.

Scientists discover hidden brain cells that may stop Alzheimer’s tau buildup

Scientists have uncovered a surprising new role for little-known brain cells called tanycytes that may influence the development of Alzheimer’s disease. These specialized cells appear to help remove toxic tau protein from the brain by transporting it from the cerebrospinal fluid into the bloodstream. When tanycytes become damaged or dysfunctional, tau can accumulate in the brain, a hallmark of Alzheimer’s.

Transhumanism: the future or the world’s most dangerous idea?

For centuries we treated technology as a tool, and now a new movement insists it is becoming the future of the human species itself.

Transhumanists like Harari and Kurzweil predict the merger of humans and machines, even the rise of a “digital God.” But critics fear this proposed future, calling transhumanism “the world’s most dangerous idea.”

Is the future one where technology is not merely a source of innovation but the basis for a new account of what it is to be human, or are claims of eternal life and new forms of intelligence just fanciful nonsense?

Joining the debate are transhumanist pioneer Zoltan Istvan, physicist and consciousness researcher Àlex Gómez-Marín, philosopher of mind Susan Schneider, and Softmax co-founder Adam Goldstein.

Tap the link now to watch the full debate.


We have for centuries sought technological progress. But now some are making the radical claim that technology is the future of the human race. ‘Effective accelerationists’ have won high-profile Silicon Valley support and claim we should accelerate technology to.

Stem Cell Treatments For Parkinson’s And Heart Failure Approved in World First

Japan has approved ground-breaking stem-cell treatments for Parkinson’s and severe heart failure, one of the manufacturers and media reports said Friday, with the therapies expected to reach patients within months.

Pharmaceutical company Sumitomo Pharma said it received the green light for the manufacture and sale of Amchepry, its Parkinson’s disease treatment that transplants stem cells into a patient’s brain.

Japan’s health ministry also gave the go-ahead to ReHeart, heart muscle sheets developed by medical startup Cuorips that can help form new blood vessels and restore heart function, media reports said.

Cancer drug reduces early Alzheimer’s-like brain hyperconnectivity in lab tests

Neuroscientists at King’s College London have pinpointed a mechanism behind the increased neural connectivity observed in the very early stages of Alzheimer’s disease. Published in Translational Psychiatry, the study also demonstrated that a cancer medication has the potential to reduce this hyperconnectivity.

The research showed that low levels of the protein amyloid-beta could induce hyperconnectivity and this pattern closely resembled changes seen in the brains of people with mild cognitive impairment (MCI). Amyloid-beta is thought to be instrumental in Alzheimer’s disease, where it creates plaques—or sticky clumps of amyloid-beta proteins—around the neurons.

These new findings suggest that low levels of amyloid-beta alone are enough to trigger early, disease-relevant changes in how brain cells connect.

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