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  1. Article: De novo serine synthesis regulates chondrocyte proliferation during bone development and repair.

    Stegen, Steve / Loopmans, Shauni / Stockmans, Ingrid / Moermans, Karen / Carmeliet, Peter / Carmeliet, Geert

    Bone research

    2022  Volume 10, Issue 1, Page(s) 14

    Abstract: The majority of the mammalian skeleton is formed through endochondral ossification starting from a cartilaginous template. Cartilage cells, or chondrocytes, survive, proliferate and synthesize extracellular matrix in an avascular environment, but the ... ...

    Abstract The majority of the mammalian skeleton is formed through endochondral ossification starting from a cartilaginous template. Cartilage cells, or chondrocytes, survive, proliferate and synthesize extracellular matrix in an avascular environment, but the metabolic requirements for these anabolic processes are not fully understood. Here, using metabolomics analysis and genetic in vivo models, we show that maintaining intracellular serine homeostasis is essential for chondrocyte function. De novo serine synthesis through phosphoglycerate dehydrogenase (PHGDH)-mediated glucose metabolism generates nucleotides that are necessary for chondrocyte proliferation and long bone growth. On the other hand, dietary serine is less crucial during endochondral bone formation, as serine-starved chondrocytes compensate by inducing PHGDH-mediated serine synthesis. Mechanistically, this metabolic flexibility requires ATF4, a transcriptional regulator of amino acid metabolism and stress responses. We demonstrate that both serine deprivation and PHGDH inactivation enhance ATF4 signaling to stimulate de novo serine synthesis and serine uptake, respectively, and thereby prevent intracellular serine depletion and chondrocyte dysfunction. A similar metabolic adaptability between serine uptake and de novo synthesis is observed in the cartilage callus during fracture repair. Together, the results of this study reveal a critical role for PHGDH-dependent serine synthesis in maintaining intracellular serine levels under physiological and serine-limited conditions, as adequate serine levels are necessary to support chondrocyte proliferation during endochondral ossification.
    Language English
    Publishing date 2022-02-15
    Publishing country China
    Document type Journal Article
    ZDB-ID 2803313-9
    ISSN 2095-6231 ; 2095-4700
    ISSN (online) 2095-6231
    ISSN 2095-4700
    DOI 10.1038/s41413-021-00185-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Immunomodulation by endothelial cells - partnering up with the immune system?

    Amersfoort, Jacob / Eelen, Guy / Carmeliet, Peter

    Nature reviews. Immunology

    2022  Volume 22, Issue 9, Page(s) 576–588

    Abstract: Blood vessel endothelial cells (ECs) have long been known to modulate inflammation by regulating immune cell trafficking, activation status and function. However, whether the heterogeneous EC populations in various tissues and organs differ in their ... ...

    Abstract Blood vessel endothelial cells (ECs) have long been known to modulate inflammation by regulating immune cell trafficking, activation status and function. However, whether the heterogeneous EC populations in various tissues and organs differ in their immunomodulatory capacity has received insufficient attention, certainly with regard to considering them for alternative immunotherapy. Recent single-cell studies have identified specific EC subtypes that express gene signatures indicative of phagocytosis or scavenging, antigen presentation and immune cell recruitment. Here we discuss emerging evidence suggesting a tissue-specific and vessel type-specific immunomodulatory role for distinct subtypes of ECs, here collectively referred to as 'immunomodulatory ECs' (IMECs). We propose that IMECs have more important functions in immunity than previously recognized, and suggest that these might be considered as targets for new immunotherapeutic approaches.
    MeSH term(s) Antigen Presentation ; Endothelial Cells ; Humans ; Immune System ; Immunomodulation ; Inflammation
    Language English
    Publishing date 2022-03-14
    Publishing country England
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 2062776-2
    ISSN 1474-1741 ; 1474-1733
    ISSN (online) 1474-1741
    ISSN 1474-1733
    DOI 10.1038/s41577-022-00694-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: A Role for the Vascular Endothelium in Post-Acute COVID-19?

    de Rooij, Laura P M H / Becker, Lisa M / Carmeliet, Peter

    Circulation

    2022  Volume 145, Issue 20, Page(s) 1503–1505

    MeSH term(s) Angiotensin-Converting Enzyme 2 ; COVID-19 ; Endothelium ; Endothelium, Vascular ; Humans ; SARS-CoV-2
    Chemical Substances Angiotensin-Converting Enzyme 2 (EC 3.4.17.23)
    Language English
    Publishing date 2022-05-16
    Publishing country United States
    Document type News ; Research Support, Non-U.S. Gov't
    ZDB-ID 80099-5
    ISSN 1524-4539 ; 0009-7322 ; 0069-4193 ; 0065-8499
    ISSN (online) 1524-4539
    ISSN 0009-7322 ; 0069-4193 ; 0065-8499
    DOI 10.1161/CIRCULATIONAHA.122.059231
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Metabolic Reprogramming in Tumor Endothelial Cells.

    García-Caballero, Melissa / Sokol, Liliana / Cuypers, Anne / Carmeliet, Peter

    International journal of molecular sciences

    2022  Volume 23, Issue 19

    Abstract: The dynamic crosstalk between the different components of the tumor microenvironment is critical to determine cancer progression, metastatic dissemination, tumor immunity, and therapeutic responses. Angiogenesis is critical for tumor growth, and abnormal ...

    Abstract The dynamic crosstalk between the different components of the tumor microenvironment is critical to determine cancer progression, metastatic dissemination, tumor immunity, and therapeutic responses. Angiogenesis is critical for tumor growth, and abnormal blood vessels contribute to hypoxia and acidosis in the tumor microenvironment. In this hostile environment, cancer and stromal cells have the ability to alter their metabolism in order to support the high energetic demands and favor rapid tumor proliferation. Recent advances have shown that tumor endothelial cell metabolism is reprogrammed, and that targeting endothelial metabolic pathways impacts developmental and pathological vessel sprouting. Therefore, the use of metabolic antiangiogenic therapies to normalize the blood vasculature, in combination with immunotherapies, offers a clinical niche to treat cancer.
    MeSH term(s) Endothelial Cells/metabolism ; Humans ; Immunotherapy ; Neoplasms/pathology ; Neovascularization, Pathologic/pathology ; Tumor Microenvironment
    Language English
    Publishing date 2022-09-21
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms231911052
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Late Clinical Valve Thrombosis After Transcatheter Aortic Valve Replacement Despite Non-Vitamin K Anticoagulant.

    Carmeliet, Tom / Vermeersch, Paul / Prihadi, Edgard A

    JACC. Case reports

    2021  Volume 3, Issue 10, Page(s) 1275–1280

    Abstract: This study presents the case of a late clinical leaflet thrombosis 1.5 years after percutaneous aortic valve replacement, despite adequate non-vitamin K anticoagulant therapy. Optimal antithrombotic therapy after transcatheter aortic valve replacement ... ...

    Abstract This study presents the case of a late clinical leaflet thrombosis 1.5 years after percutaneous aortic valve replacement, despite adequate non-vitamin K anticoagulant therapy. Optimal antithrombotic therapy after transcatheter aortic valve replacement remains undetermined. After switching to vitamin K antagonist therapy, complete resolution occurred at 3 months follow-up. (
    Language English
    Publishing date 2021-08-19
    Publishing country Netherlands
    Document type Case Reports
    ISSN 2666-0849
    ISSN (online) 2666-0849
    DOI 10.1016/j.jaccas.2021.06.012
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Endothelial metabolism going single.

    Subramanian, Abhishek / Becker, Lisa M / Carmeliet, Peter

    Nature metabolism

    2021  Volume 3, Issue 5, Page(s) 593–594

    Language English
    Publishing date 2021-05-24
    Publishing country Germany
    Document type Journal Article
    ISSN 2522-5812
    ISSN (online) 2522-5812
    DOI 10.1038/s42255-021-00399-3
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Targeting hypoxia-inducible factors: therapeutic opportunities and challenges.

    Yuan, Xiaoyi / Ruan, Wei / Bobrow, Bentley / Carmeliet, Peter / Eltzschig, Holger K

    Nature reviews. Drug discovery

    2023  Volume 23, Issue 3, Page(s) 175–200

    Abstract: Hypoxia-inducible factors (HIFs) are highly conserved transcription factors that are crucial for adaptation of metazoans to limited oxygen availability. Recently, HIF activation and inhibition have emerged as therapeutic targets in various human diseases. ...

    Abstract Hypoxia-inducible factors (HIFs) are highly conserved transcription factors that are crucial for adaptation of metazoans to limited oxygen availability. Recently, HIF activation and inhibition have emerged as therapeutic targets in various human diseases. Pharmacologically desirable effects of HIF activation include erythropoiesis stimulation, cellular metabolism optimization during hypoxia and adaptive responses during ischaemia and inflammation. By contrast, HIF inhibition has been explored as a therapy for various cancers, retinal neovascularization and pulmonary hypertension. This Review discusses the biochemical mechanisms that control HIF stabilization and the molecular strategies that can be exploited pharmacologically to activate or inhibit HIFs. In addition, we examine medical conditions that benefit from targeting HIFs, the potential side effects of HIF activation or inhibition and future challenges in this field.
    MeSH term(s) Humans ; Basic Helix-Loop-Helix Transcription Factors ; Hypoxia/drug therapy ; Hypoxia/metabolism ; Transcription Factors ; Neoplasms/drug therapy ; Oxygen
    Chemical Substances Basic Helix-Loop-Helix Transcription Factors ; Transcription Factors ; Oxygen (S88TT14065)
    Language English
    Publishing date 2023-12-20
    Publishing country England
    Document type Journal Article ; Review ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 2062954-0
    ISSN 1474-1784 ; 1474-1776
    ISSN (online) 1474-1784
    ISSN 1474-1776
    DOI 10.1038/s41573-023-00848-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: The role of endothelial cells in cystic fibrosis.

    Declercq, M / Treps, L / Carmeliet, P / Witters, P

    Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

    2019  Volume 18, Issue 6, Page(s) 752–761

    Abstract: Cystic fibrosis (CF) is an autosomal recessive disease caused by the loss of function of the cystic fibrosis transmembrane conductance regulator (CFTR) protein which primarily acts as a chloride channel. CFTR has mainly been studied in epithelial cells ... ...

    Abstract Cystic fibrosis (CF) is an autosomal recessive disease caused by the loss of function of the cystic fibrosis transmembrane conductance regulator (CFTR) protein which primarily acts as a chloride channel. CFTR has mainly been studied in epithelial cells although it is also functional and expressed in other cell types including endothelial cells. The present review summarizes current knowledge on the role of the endothelium in CF. More specifically, this review highlights the role of endothelial cells in CF in acting as a semipermeable barrier, as a key regulator of angiogenesis, coagulation, the vascular tone and the inflammatory responses. It could contribute to different aspects of the disease including cardiovascular symptoms, excessive blood vessel formation, pulmonary and portal hypertension and CF-related diabetes. Despite the important role of vascular endothelium in many biological processes, it has largely been under investigated in CF.
    MeSH term(s) Cell Membrane Permeability ; Cystic Fibrosis/metabolism ; Cystic Fibrosis/pathology ; Cystic Fibrosis/physiopathology ; Cystic Fibrosis Transmembrane Conductance Regulator/metabolism ; Endothelial Cells/physiology ; Endothelial Cells/ultrastructure ; Humans
    Chemical Substances CFTR protein, human ; Cystic Fibrosis Transmembrane Conductance Regulator (126880-72-6)
    Language English
    Publishing date 2019-08-07
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2084724-5
    ISSN 1873-5010 ; 1569-1993
    ISSN (online) 1873-5010
    ISSN 1569-1993
    DOI 10.1016/j.jcf.2019.07.005
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  9. Article ; Online: Glutamine Metabolism in Osteoprogenitors Is Required for Bone Mass Accrual and PTH-Induced Bone Anabolism in Male Mice.

    Stegen, Steve / Devignes, Claire-Sophie / Torrekens, Sophie / Van Looveren, Riet / Carmeliet, Peter / Carmeliet, Geert

    Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research

    2020  Volume 36, Issue 3, Page(s) 604–616

    Abstract: Skeletal homeostasis critically depends on the proper anabolic functioning of osteolineage cells. Proliferation and matrix synthesis are highly demanding in terms of biosynthesis and bioenergetics, but the nutritional requirements that support these ... ...

    Abstract Skeletal homeostasis critically depends on the proper anabolic functioning of osteolineage cells. Proliferation and matrix synthesis are highly demanding in terms of biosynthesis and bioenergetics, but the nutritional requirements that support these processes in bone-forming cells are not fully understood. Here, we show that glutamine metabolism is a major determinant of osteoprogenitor function during bone mass accrual. Genetic inactivation of the rate-limiting enzyme glutaminase 1 (GLS1) results in decreased postnatal bone mass, caused by impaired biosynthesis and cell survival. Mechanistically, we uncovered that GLS1-mediated glutamine catabolism supports nucleotide and amino acid synthesis, required for proliferation and matrix production. In addition, glutamine-derived glutathione prevents accumulation of reactive oxygen species and thereby safeguards cell viability. The pro-anabolic role of glutamine metabolism was further underscored in a model of parathyroid hormone (PTH)-induced bone formation. PTH administration increases glutamine uptake and catabolism, and GLS1 deletion fully blunts the PTH-induced osteoanabolic response. Taken together, our findings indicate that glutamine metabolism in osteoprogenitors is indispensable for bone formation. © 2020 American Society for Bone and Mineral Research (ASBMR).
    MeSH term(s) Animals ; Bone Density ; Glutaminase ; Glutamine ; Male ; Mice ; Osteoblasts ; Osteogenesis ; Parathyroid Hormone
    Chemical Substances Parathyroid Hormone ; Glutamine (0RH81L854J) ; Glutaminase (EC 3.5.1.2)
    Language English
    Publishing date 2020-12-18
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 632783-7
    ISSN 1523-4681 ; 0884-0431
    ISSN (online) 1523-4681
    ISSN 0884-0431
    DOI 10.1002/jbmr.4219
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  10. Article ; Online: Shaping the brain vasculature in development and disease in the single-cell era.

    Wälchli, Thomas / Bisschop, Jeroen / Carmeliet, Peter / Zadeh, Gelareh / Monnier, Philippe P / De Bock, Katrien / Radovanovic, Ivan

    Nature reviews. Neuroscience

    2023  Volume 24, Issue 5, Page(s) 271–298

    Abstract: The CNS critically relies on the formation and proper function of its vasculature during development, adult homeostasis and disease. Angiogenesis - the formation of new blood vessels - is highly active during brain development, enters almost complete ... ...

    Abstract The CNS critically relies on the formation and proper function of its vasculature during development, adult homeostasis and disease. Angiogenesis - the formation of new blood vessels - is highly active during brain development, enters almost complete quiescence in the healthy adult brain and is reactivated in vascular-dependent brain pathologies such as brain vascular malformations and brain tumours. Despite major advances in the understanding of the cellular and molecular mechanisms driving angiogenesis in peripheral tissues, developmental signalling pathways orchestrating angiogenic processes in the healthy and the diseased CNS remain incompletely understood. Molecular signalling pathways of the 'neurovascular link' defining common mechanisms of nerve and vessel wiring have emerged as crucial regulators of peripheral vascular growth, but their relevance for angiogenesis in brain development and disease remains largely unexplored. Here we review the current knowledge of general and CNS-specific mechanisms of angiogenesis during brain development and in brain vascular malformations and brain tumours, including how key molecular signalling pathways are reactivated in vascular-dependent diseases. We also discuss how these topics can be studied in the single-cell multi-omics era.
    MeSH term(s) Humans ; Neovascularization, Physiologic/physiology ; Brain ; Brain Neoplasms ; Signal Transduction ; Central Nervous System Vascular Malformations
    Language English
    Publishing date 2023-03-20
    Publishing country England
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 2034150-7
    ISSN 1471-0048 ; 1471-0048 ; 1471-003X
    ISSN (online) 1471-0048
    ISSN 1471-0048 ; 1471-003X
    DOI 10.1038/s41583-023-00684-y
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