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  1. Article ; Online: Endothelial Autophagy Dysregulation in Diabetes.

    Salemkour, Yann / Lenoir, Olivia

    Cells

    2023  Volume 12, Issue 6

    Abstract: Diabetes mellitus is a major public health issue that affected 537 million people worldwide in 2021, a number that is only expected to increase in the upcoming decade. Diabetes is a systemic metabolic disease with devastating macro- and microvascular ... ...

    Abstract Diabetes mellitus is a major public health issue that affected 537 million people worldwide in 2021, a number that is only expected to increase in the upcoming decade. Diabetes is a systemic metabolic disease with devastating macro- and microvascular complications. Endothelial dysfunction is a key determinant in the pathogenesis of diabetes. Dysfunctional endothelium leads to vasoconstriction by decreased nitric oxide bioavailability and increased expression of vasoconstrictor factors, vascular inflammation through the production of pro-inflammatory cytokines, a loss of microvascular density leading to low organ perfusion, procoagulopathy, and/or arterial stiffening. Autophagy, a lysosomal recycling process, appears to play an important role in endothelial cells, ensuring endothelial homeostasis and functions. Previous reports have provided evidence of autophagic flux impairment in patients with type I or type II diabetes. In this review, we report evidence of endothelial autophagy dysfunction during diabetes. We discuss the mechanisms driving endothelial autophagic flux impairment and summarize therapeutic strategies targeting autophagy in diabetes.
    MeSH term(s) Humans ; Diabetes Mellitus, Type 2/metabolism ; Endothelial Cells/metabolism ; Endothelium, Vascular/metabolism ; Vascular Diseases/metabolism ; Autophagy
    Language English
    Publishing date 2023-03-21
    Publishing country Switzerland
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 2661518-6
    ISSN 2073-4409 ; 2073-4409
    ISSN (online) 2073-4409
    ISSN 2073-4409
    DOI 10.3390/cells12060947
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Endothelial Autophagy Dysregulation in Diabetes

    Yann Salemkour / Olivia Lenoir

    Cells, Vol 12, Iss 947, p

    2023  Volume 947

    Abstract: Diabetes mellitus is a major public health issue that affected 537 million people worldwide in 2021, a number that is only expected to increase in the upcoming decade. Diabetes is a systemic metabolic disease with devastating macro- and microvascular ... ...

    Abstract Diabetes mellitus is a major public health issue that affected 537 million people worldwide in 2021, a number that is only expected to increase in the upcoming decade. Diabetes is a systemic metabolic disease with devastating macro- and microvascular complications. Endothelial dysfunction is a key determinant in the pathogenesis of diabetes. Dysfunctional endothelium leads to vasoconstriction by decreased nitric oxide bioavailability and increased expression of vasoconstrictor factors, vascular inflammation through the production of pro-inflammatory cytokines, a loss of microvascular density leading to low organ perfusion, procoagulopathy, and/or arterial stiffening. Autophagy, a lysosomal recycling process, appears to play an important role in endothelial cells, ensuring endothelial homeostasis and functions. Previous reports have provided evidence of autophagic flux impairment in patients with type I or type II diabetes. In this review, we report evidence of endothelial autophagy dysfunction during diabetes. We discuss the mechanisms driving endothelial autophagic flux impairment and summarize therapeutic strategies targeting autophagy in diabetes.
    Keywords autophagy ; endothelial cells ; diabetes ; Biology (General) ; QH301-705.5
    Subject code 571
    Language English
    Publishing date 2023-03-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: Should we consider calcimimetics as a therapeutic option for nephrotic syndrome?

    Lenoir, Olivia / Tharaux, Pierre-Louis

    Kidney international

    2022  Volume 101, Issue 6, Page(s) 1110–1112

    Abstract: Calcimimetics allosterically increase the calcium ion sensitivity of the calcium-sensing receptor (CaSR). Using a CaSR knockdown in podocytes and a podocyte-specific CaSR knockout in mice, Mühlig et al. uncovered a stabilizing role for actin cytoskeleton ...

    Abstract Calcimimetics allosterically increase the calcium ion sensitivity of the calcium-sensing receptor (CaSR). Using a CaSR knockdown in podocytes and a podocyte-specific CaSR knockout in mice, Mühlig et al. uncovered a stabilizing role for actin cytoskeleton and cell adhesion. Short-term alleviation of albuminuria and proteinuria was observed in 4 children treated with cinacalcet. Here we discuss the potential mechanisms whereby CaSR displays a favorable effect in podocytes and the context in which calcimimetics may alleviate nephrotic syndrome.
    MeSH term(s) Animals ; Cinacalcet/pharmacology ; Cinacalcet/therapeutic use ; Mice ; Nephrotic Syndrome/drug therapy ; Nephrotic Syndrome/metabolism ; Podocytes/metabolism ; Proteinuria/drug therapy ; Proteinuria/metabolism ; Receptors, Calcium-Sensing/genetics ; Receptors, Calcium-Sensing/metabolism
    Chemical Substances Receptors, Calcium-Sensing ; Cinacalcet (UAZ6V7728S)
    Language English
    Publishing date 2022-05-18
    Publishing country United States
    Document type Journal Article ; Comment
    ZDB-ID 120573-0
    ISSN 1523-1755 ; 0085-2538
    ISSN (online) 1523-1755
    ISSN 0085-2538
    DOI 10.1016/j.kint.2022.04.008
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: From bench to bedside: lessons learned from translational podocyte research.

    Lenoir, Olivia / Huber, Tobias B / Tharaux, Pierre-Louis

    Kidney international

    2023  Volume 103, Issue 6, Page(s) 1018–1020

    Abstract: Polat et al. report that mice with a podocyte-specific expression of a constitutively active Rac1 form displayed similar injury and albuminuria, regardless of transient receptor potential canonical 5 activity. This article confirms the pathogenic role of ...

    Abstract Polat et al. report that mice with a podocyte-specific expression of a constitutively active Rac1 form displayed similar injury and albuminuria, regardless of transient receptor potential canonical 5 activity. This article confirms the pathogenic role of deregulated Rac1 and challenges models involving the role of transient receptor potential canonical 5 in podocytes. We learned from this study and propose a roadmap for this controversial field to help new drug candidates succeed in clinical trials and safely reach patients.
    MeSH term(s) Mice ; Animals ; Podocytes/pathology ; Albuminuria/metabolism
    Language English
    Publishing date 2023-03-21
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Comment
    ZDB-ID 120573-0
    ISSN 1523-1755 ; 0085-2538
    ISSN (online) 1523-1755
    ISSN 0085-2538
    DOI 10.1016/j.kint.2023.03.008
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Podocyte healthy self-eating boosted by a spermidine meal?

    Lenoir, Olivia / Tharaux, Pierre-Louis

    Kidney international

    2020  Volume 98, Issue 6, Page(s) 1390–1392

    Abstract: The mechanisms sustaining a high level of autophagy in podocytes are not well delineated. Seminal studies had unraveled that the polyamine pathway is involved in the regulation of aging and autophagy. Polyamines (e.g., spermine, spermidine, and ... ...

    Abstract The mechanisms sustaining a high level of autophagy in podocytes are not well delineated. Seminal studies had unraveled that the polyamine pathway is involved in the regulation of aging and autophagy. Polyamines (e.g., spermine, spermidine, and putrescine) are ubiquitous molecules essential for the physiological processes, including cell growth, development, and differentiation. Liang et al. examined the role of ornithine decarboxylase, and spermidine synthase, and demonstrated that endogenous spermidine is required to maintain intact podocyte autophagy.
    MeSH term(s) Adenosylmethionine Decarboxylase ; Autophagy ; Cell Division ; Podocytes ; Spermidine
    Chemical Substances Adenosylmethionine Decarboxylase (EC 4.1.1.50) ; Spermidine (U87FK77H25)
    Language English
    Publishing date 2020-12-04
    Publishing country United States
    Document type Journal Article ; Comment
    ZDB-ID 120573-0
    ISSN 1523-1755 ; 0085-2538
    ISSN (online) 1523-1755
    ISSN 0085-2538
    DOI 10.1016/j.kint.2020.07.032
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Glomerular Endothelial Cell Crosstalk With Podocytes in Diabetic Kidney Disease.

    Mahtal, Nassim / Lenoir, Olivia / Tharaux, Pierre-Louis

    Frontiers in medicine

    2021  Volume 8, Page(s) 659013

    Abstract: Diabetes is the main cause of renal failure worldwide. Complications of the kidney micro-and macro-circulation are common in diabetic patients, leading to proteinuria and can progress to end-stage renal disease. Across the complex interplays aggravating ... ...

    Abstract Diabetes is the main cause of renal failure worldwide. Complications of the kidney micro-and macro-circulation are common in diabetic patients, leading to proteinuria and can progress to end-stage renal disease. Across the complex interplays aggravating diabetes kidney disease progression, lesions of the glomerular filtration barrier appear crucial. Among its components, glomerular endothelial cells are known to be central safeguards of plasma filtration. An array of evidence has recently pinpointed its intricate relations with podocytes, highly specialized pericytes surrounding glomerular capillaries. During diabetic nephropathy, endothelial cells and podocytes are stressed and damaged. Besides, each can communicate with the other, directly affecting the progression of glomerular injury. Here, we review recent studies showing how
    Language English
    Publishing date 2021-03-24
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2775999-4
    ISSN 2296-858X
    ISSN 2296-858X
    DOI 10.3389/fmed.2021.659013
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Parietal epithelial cells role in repair versus scarring after glomerular injury.

    Lazareth, Hélène / Lenoir, Olivia / Tharaux, Pierre-Louis

    Current opinion in nephrology and hypertension

    2020  Volume 29, Issue 3, Page(s) 293–301

    Abstract: Purpose of review: The recent years have been marked by the publication of several articles highlighting the pathophysiological role of glomerular parietal epithelial cells (PEC) and refining their phenotypic heterogeneity.: Recent findings: The ... ...

    Abstract Purpose of review: The recent years have been marked by the publication of several articles highlighting the pathophysiological role of glomerular parietal epithelial cells (PEC) and refining their phenotypic heterogeneity.
    Recent findings: The present review synthetizes recent findings on (i) the potential regenerative role of PEC in glomerular diseases, and (ii) the mechanisms and signaling of leading to PEC pathogenic involvement in crescentic glomerulonephritis (CGN) and focal segmental glomerulosclerosis (FSGS).
    Summary: The debate is still open regarding the podocyte regenerative properties of PEC in glomerular disease, whereas the pathogenic involvement of PEC activation in glomerular disease is increasingly admitted. Recent highlights on the podocyte regenerative role of PEC, on one hand, and on their pathological function, on the other hand, for sure will feed the debate in the kidney community for the next years. Nevertheless, from a therapeutic perspective, the two options, boosting cellular regeneration and blocking PECs pathogenicity, should not be seen as antagonistic but, rather, complementary.
    MeSH term(s) Animals ; Cicatrix/etiology ; Glomerulonephritis/physiopathology ; Glomerulosclerosis, Focal Segmental/physiopathology ; Humans ; Kidney Glomerulus/physiology ; Podocytes/physiology ; Regeneration ; Signal Transduction/physiology
    Language English
    Publishing date 2020-03-28
    Publishing country England
    Document type Comparative Study ; Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 1151092-4
    ISSN 1473-6543 ; 1535-3842 ; 1062-4813 ; 1062-4821
    ISSN (online) 1473-6543 ; 1535-3842
    ISSN 1062-4813 ; 1062-4821
    DOI 10.1097/MNH.0000000000000600
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: MicroRNAs in kidney injury and disease.

    Mahtal, Nassim / Lenoir, Olivia / Tinel, Claire / Anglicheau, Dany / Tharaux, Pierre-Louis

    Nature reviews. Nephrology

    2022  Volume 18, Issue 10, Page(s) 643–662

    Abstract: MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression by degrading or repressing the translation of their target messenger RNAs. As miRNAs are critical regulators of cellular homeostasis, their dysregulation is a crucial component of ...

    Abstract MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression by degrading or repressing the translation of their target messenger RNAs. As miRNAs are critical regulators of cellular homeostasis, their dysregulation is a crucial component of cell and organ injury. A substantial body of evidence indicates that miRNAs are involved in the pathophysiology of acute kidney injury (AKI), chronic kidney disease and allograft damage. Different subsets of miRNAs are dysregulated during AKI, chronic kidney disease and allograft rejection, which could reflect differences in the physiopathology of these conditions. miRNAs that have been investigated in AKI include miR-21, which has an anti-apoptotic role, and miR-214 and miR-668, which regulate mitochondrial dynamics. Various miRNAs are downregulated in diabetic kidney disease, including the miR-30 family and miR-146a, which protect against inflammation and fibrosis. Other miRNAs such as miR-193 and miR-92a induce podocyte dedifferentiation in glomerulonephritis. In transplantation, miRNAs have been implicated in allograft rejection and injury. Further work is needed to identify and validate miRNAs as biomarkers of graft function and of kidney disease development and progression. Use of combinations of miRNAs together with other molecular markers could potentially improve diagnostic or predictive power and facilitate clinical translation. In addition, targeting specific miRNAs at different stages of disease could be a promising therapeutic strategy.
    MeSH term(s) Acute Kidney Injury/genetics ; Acute Kidney Injury/pathology ; Biomarkers/metabolism ; Humans ; Kidney/metabolism ; MicroRNAs/genetics ; MicroRNAs/metabolism ; Renal Insufficiency, Chronic/genetics ; Renal Insufficiency, Chronic/pathology
    Chemical Substances Biomarkers ; MIRN214 microRNA, human ; MicroRNAs
    Language English
    Publishing date 2022-08-16
    Publishing country England
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 2490366-8
    ISSN 1759-507X ; 1759-5061
    ISSN (online) 1759-507X
    ISSN 1759-5061
    DOI 10.1038/s41581-022-00608-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Immunofluorescence staining of WT-1/Podocalyxin on Mouse kidney sections.

    Henique, Carole / Lenoir, Olivia / Tharaux, Pierre-Louis

    Bio-protocol

    2019  Volume 9, Issue 8, Page(s) e3210

    Abstract: In glomerular diseases, podocytes are one type of cells involved in dysfunction of glomerular filtration. In these conditions, podocyte proteins expression change. Therefore, immunofluorescent staining of podocytes can be performed to visualize podocyte ... ...

    Abstract In glomerular diseases, podocytes are one type of cells involved in dysfunction of glomerular filtration. In these conditions, podocyte proteins expression change. Therefore, immunofluorescent staining of podocytes can be performed to visualize podocyte localization of proteins of interest. In this protocol, we detail a method to stain podocytes with a specific marker WT-1 (
    Language English
    Publishing date 2019-04-20
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2833269-6
    ISSN 2331-8325 ; 2331-8325
    ISSN (online) 2331-8325
    ISSN 2331-8325
    DOI 10.21769/BioProtoc.3210
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Rôle pathogénique de l’expression anormale de la tétraspanine CD9 par les cellules épithéliales pariétales dans les glomérulopathies extracapillaires.

    Lazareth, Hélène / Lenoir, Olivia / Hénique, Carole / Bouzigues, Cédric / Boucheix, Claude / Tharaux, Pierre-Louis

    Medecine sciences : M/S

    2020  Volume 36, Issue 10, Page(s) 852–855

    Title translation De novo expression of tetraspanin CD9 in parietal epithelial cells promotes extracapillary glomerulonephritis.
    MeSH term(s) Animals ; Disease Models, Animal ; Epithelial Cells/metabolism ; Glomerulonephritis/genetics ; Glomerulonephritis/metabolism ; Glomerulonephritis/pathology ; Humans ; Kidney Glomerulus/metabolism ; Mice ; Mice, Transgenic ; Tetraspanin 29/genetics ; Tetraspanin 29/metabolism
    Chemical Substances Cd9 protein, mouse ; Tetraspanin 29
    Language French
    Publishing date 2020-10-07
    Publishing country France
    Document type News
    ZDB-ID 632733-3
    ISSN 1958-5381 ; 0767-0974
    ISSN (online) 1958-5381
    ISSN 0767-0974
    DOI 10.1051/medsci/2020154
    Database MEDical Literature Analysis and Retrieval System OnLINE

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