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Genetic ‘switches’ could program 3D-printed bone tissue for blood vessel growth

Researchers at Penn State have developed genetic 'switches' that can program 3D-printed bone tissue to grow blood vessels, enabling the regeneration of bone tissue in severe trauma or infections. The technique uses microRNA molecules to push cells down a differentiation pathway optimized for either tissue growth or vascularization.

SourcePenn State·JournalChemical Engineering Journal·TypeExperimental study·DateAug 18, 2026

Wyss Institute-led collaboration awarded by ARPA-H PRINT program to engineer off-the-shelf, universal, transplant-ready graft for liver failure

A multidisciplinary team of world-leading experts is developing an off-the-shelf engineered product that could address liver failure in millions of patients. The ImPLANT project aims to create synthetic biology-based gene circuits in human induced pluripotent stem cells to drive cell differentiation into all required liver cell types.

Novel study uncovers the critical role of ADAM10 protein in the development of retinal disorders

A recent study published in The American Journal of Pathology has discovered that ADAM10 regulates abnormal blood vessel growth in the retina, which can cause vision loss or impairment. The findings suggest that targeting ADAM10 or its downstream effectors, such as Ephrin B2, may offer novel strategies for managing or preventing retina...

SourceElsevier·JournalAmerican Journal Of Pathology·TypeExperimental study·DateJun 24, 2025

First vascularized model of stem cell islet cells

Scientists have created a vascularized organoid model of hormone-secreting cells in the pancreas, promising to improve diabetes research and cell-based therapies. The model, developed by Max Delbrück Center researchers, contains greater numbers of mature beta cells and secretes more insulin than non-vascularized counterparts.

SourceMax Delbrück Center for Molecular Medicine in the Helmholtz Association·JournalDevelopmental Cell·TypeExperimental study·DateMay 23, 2025

Aging | Genetic deficiency and pharmacological modulation of RORα regulate laser-induced choroidal neovascularization

In a mouse model of laser-induced CNV, RORα expression was highly increased in the choroidal/RPE complex post-laser, while loss or inhibition of RORα worsened CNV with increased lesion size and vascular leakage. RORα negatively regulates pathological CNV development by modulating angiogenic response and inflammatory environment.

SourceImpact Journals LLC·JournalAging-US·TypeObservational study·DateJan 18, 2023

Chinese Medical Journal editorial probes into the role of blood vessels in treating obesity-related disorders

Researchers explore the interactions between adipose tissues and surrounding blood vessels in connection with lipid metabolism and associated diseases. Targeting angiogenesis may provide a gateway for treating obesity, while its inhibition or promotion depends on the specific disease context.

SourceCactus Communications·JournalChinese Medical Journal·TypeLiterature review·DateNov 22, 2022

JCI early table of contents for April 8, 2013

Researchers identify ATRX as a crucial gene in maintaining genomic stability, preventing chromosomal mutations and rearrangements that can cause disease and aging. Atrx deficiency in mice leads to increased DNA damage, endocrine dysfunction, shortened lifespans, and degenerative phenotypes similar to human premature aging disorders.

SourceJCI Journals·JournalJournal of Clinical Investigation·DateApr 8, 2013

Animal studies show CA4P suppresses development and induces regression of ocular neovascularization

Researchers used transgenic mice to study CA4P's effect on choroidal neovascularization, finding it suppressed development and induced partial regression of established CNV. CA4P joins a growing list of drugs with potential as prophylactic agents for retinal and/or choroidal neovascularization.

SourceSharon Merrill Associates, Inc.·JournalInvestigative Ophthalmology & Visual Science·DateJul 31, 2003