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  1. Article: The Glomerular Endothelium Restricts Albumin Filtration.

    Ballermann, Barbara J / Nyström, Jenny / Haraldsson, Börje

    Frontiers in medicine

    2021  Volume 8, Page(s) 766689

    Abstract: Inflammatory activation and/or dysfunction of the glomerular endothelium triggers proteinuria in many systemic and localized vascular disorders. Among them are the thrombotic microangiopathies, many forms of glomerulonephritis, and acute inflammatory ... ...

    Abstract Inflammatory activation and/or dysfunction of the glomerular endothelium triggers proteinuria in many systemic and localized vascular disorders. Among them are the thrombotic microangiopathies, many forms of glomerulonephritis, and acute inflammatory episodes like sepsis and COVID-19 illness. Another example is the chronic endothelial dysfunction that develops in cardiovascular disease and in metabolic disorders like diabetes. While the glomerular endothelium is a porous sieve that filters prodigious amounts of water and small solutes, it also bars the bulk of albumin and large plasma proteins from passing into the glomerular filtrate. This endothelial barrier function is ascribed predominantly to the endothelial glycocalyx with its endothelial surface layer, that together form a relatively thick, mucinous coat composed of glycosaminoglycans, proteoglycans, glycolipids, sialomucins and other glycoproteins, as well as secreted and circulating proteins. The glycocalyx/endothelial surface layer not only covers the glomerular endothelium; it extends into the endothelial fenestrae. Some glycocalyx components span or are attached to the apical endothelial cell plasma membrane and form the formal glycocalyx. Other components, including small proteoglycans and circulating proteins like albumin and orosomucoid, form the endothelial surface layer and are bound to the glycocalyx due to weak intermolecular interactions. Indeed, bound plasma albumin is a major constituent of the endothelial surface layer and contributes to its barrier function. A role for glomerular endothelial cells in the barrier of the glomerular capillary wall to protein filtration has been demonstrated by many elegant studies. However, it can only be fully understood in the context of other components, including the glomerular basement membrane, the podocytes and reabsorption of proteins by tubule epithelial cells. Discovery of the precise mechanisms that lead to glycocalyx/endothelial surface layer disruption within glomerular capillaries will hopefully lead to pharmacological interventions that specifically target this important structure.
    Language English
    Publishing date 2021-11-29
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2775999-4
    ISSN 2296-858X
    ISSN 2296-858X
    DOI 10.3389/fmed.2021.766689
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: An In Vitro Kinase Assay to Assess Rac1 Phosphorylation by ERK.

    Brandwein, Daniel / Tong, Junfeng / Li, Laiji / Ballermann, Barbara / Wang, Zhixiang

    Methods in molecular biology (Clifton, N.J.)

    2018  Volume 1821, Page(s) 131–140

    Abstract: Recent findings suggest that phosphorylation might further contribute to the tight regulation of Rho GTPases. Interestingly, sequence analysis of Rac1 shows that T108 within ... ...

    Abstract Recent findings suggest that phosphorylation might further contribute to the tight regulation of Rho GTPases. Interestingly, sequence analysis of Rac1 shows that T108 within the
    MeSH term(s) Adenosine Triphosphate/chemistry ; Amino Acid Motifs ; Extracellular Signal-Regulated MAP Kinases/chemistry ; Extracellular Signal-Regulated MAP Kinases/genetics ; Extracellular Signal-Regulated MAP Kinases/metabolism ; Humans ; Isotope Labeling/methods ; Phosphorylation ; Recombinant Fusion Proteins/chemistry ; Recombinant Fusion Proteins/genetics ; Recombinant Fusion Proteins/metabolism ; rac1 GTP-Binding Protein/chemistry ; rac1 GTP-Binding Protein/genetics ; rac1 GTP-Binding Protein/metabolism
    Chemical Substances RAC1 protein, human ; Recombinant Fusion Proteins ; Adenosine Triphosphate (8L70Q75FXE) ; Extracellular Signal-Regulated MAP Kinases (EC 2.7.11.24) ; rac1 GTP-Binding Protein (EC 3.6.5.2)
    Language English
    Publishing date 2018-07-31
    Publishing country United States
    Document type Journal Article
    ISSN 1940-6029
    ISSN (online) 1940-6029
    DOI 10.1007/978-1-4939-8612-5_9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Phosphorylation and Activation of RhoA by ERK in Response to Epidermal Growth Factor Stimulation.

    Tong, Junfeng / Li, Laiji / Ballermann, Barbara / Wang, Zhixiang

    PloS one

    2016  Volume 11, Issue 1, Page(s) e0147103

    Abstract: The small GTPase RhoA has been implicated in various cellular activities, including the formation of stress fibers, cell motility, and cytokinesis. In addition to the canonical GTPase cycle, recent findings have suggested that phosphorylation further ... ...

    Abstract The small GTPase RhoA has been implicated in various cellular activities, including the formation of stress fibers, cell motility, and cytokinesis. In addition to the canonical GTPase cycle, recent findings have suggested that phosphorylation further contributes to the tight regulation of Rho GTPases. Indeed, RhoA is phosphorylated on serine 188 (188S) by a number of protein kinases. We have recently reported that Rac1 is phosphorylated on threonine 108 (108T) by extracellular signal-regulated kinases (ERK) in response to epidermal growth factor (EGF) stimulation. Here, we provide evidence that RhoA is phosphorylated by ERK on 88S and 100T in response to EGF stimulation. We show that ERK interacts with RhoA and that this interaction is dependent on the ERK docking site (D-site) at the C-terminus of RhoA. EGF stimulation enhanced the activation of the endogenous RhoA. The phosphomimetic mutant, GFP-RhoA S88E/T100E, when transiently expressed in COS-7 cells, displayed higher GTP-binding than wild type RhoA. Moreover, the expression of GFP-RhoA S88E/T100E increased actin stress fiber formation in COS-7 cells, which is consistent with its higher activity. In contrast to Rac1, phosphorylation of RhoA by ERK does not target RhoA to the nucleus. Finally, we show that regardless of the phosphorylation status of RhoA and Rac1, substitution of the RhoA PBR with the Rac1 PBR targets RhoA to the nucleus and substitution of Rac1 PBR with RhoA PBR significantly reduces the nuclear localization of Rac1. In conclusion, ERK phosphorylates RhoA on 88S and 100T in response to EGF, which upregulates RhoA activity.
    MeSH term(s) Actins/metabolism ; Animals ; COS Cells ; Cell Line ; Cell Nucleus/metabolism ; Cercopithecus aethiops ; Cytoskeleton/metabolism ; Epidermal Growth Factor/pharmacology ; Extracellular Signal-Regulated MAP Kinases/metabolism ; Humans ; Phosphorylation/drug effects ; Signal Transduction/drug effects ; rhoA GTP-Binding Protein/metabolism
    Chemical Substances Actins ; Epidermal Growth Factor (62229-50-9) ; Extracellular Signal-Regulated MAP Kinases (EC 2.7.11.24) ; rhoA GTP-Binding Protein (EC 3.6.5.2)
    Language English
    Publishing date 2016-01-27
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1932-6203
    ISSN (online) 1932-6203
    DOI 10.1371/journal.pone.0147103
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: TIMAP inhibits endothelial myosin light chain phosphatase by competing with MYPT1 for the catalytic protein phosphatase 1 subunit PP1cβ.

    Wang, Xin / Obeidat, Marya / Li, Laiji / Pasarj, Phuwadet / Aburahess, Salah / Holmes, Charles F B / Ballermann, Barbara J

    The Journal of biological chemistry

    2019  Volume 294, Issue 36, Page(s) 13280–13291

    Abstract: Transforming growth factor-β membrane associated protein (TIMAP) is an endothelial cell (EC)-predominant PP1 regulatory subunit and a member of the myosin phosphatase target (MYPT) protein family. The MYPTs preferentially bind the catalytic protein ... ...

    Abstract Transforming growth factor-β membrane associated protein (TIMAP) is an endothelial cell (EC)-predominant PP1 regulatory subunit and a member of the myosin phosphatase target (MYPT) protein family. The MYPTs preferentially bind the catalytic protein phosphatase 1 subunit PP1cβ, forming myosin phosphatase holoenzymes. We investigated whether TIMAP/PP1cβ could also function as a myosin phosphatase. Endogenous PP1cβ, myosin light chain 2 (MLC2), and myosin IIA heavy chain coimmunoprecipitated from EC lysates with endogenous TIMAP, and endogenous MLC2 colocalized with TIMAP in EC projections. Purified recombinant GST-TIMAP interacted directly with purified recombinant His-MLC2. However, TIMAP overexpression in EC enhanced MLC2 phosphorylation, an effect not observed with a TIMAP mutant that does not bind PP1cβ. Conversely, MLC2 phosphorylation was reduced in lung lysates from TIMAP-deficient mice and upon silencing of endogenous TIMAP expression in ECs. Ectopically expressed TIMAP slowed the rate of MLC2 dephosphorylation, an effect requiring TIMAP-PP1cβ interaction. The association of MYPT1 with PP1cβ was profoundly reduced in the presence of excess TIMAP, leading to proteasomal MYPT1 degradation. In the absence of TIMAP, MYPT1-associated PP1cβ readily bound immobilized microcystin-LR, an active-site inhibitor of PP1c. By contrast, TIMAP-associated PP1cβ did not interact with microcystin-LR, indicating that the active site of PP1cβ is blocked when it is bound to TIMAP. Thus, TIMAP inhibits myosin phosphatase activity in ECs by competing with MYPT1 for PP1cβ and blocking the PP1cβ active site.
    MeSH term(s) Animals ; Biocatalysis ; Cell Line ; Endothelial Cells/metabolism ; Humans ; Membrane Proteins/metabolism ; Mice ; Mice, Inbred C57BL ; Myosin-Light-Chain Phosphatase/antagonists & inhibitors ; Myosin-Light-Chain Phosphatase/metabolism ; Protein Phosphatase 1/metabolism
    Chemical Substances Membrane Proteins ; PPP1R16B protein, human ; Protein Phosphatase 1 (EC 3.1.3.16) ; Myosin-Light-Chain Phosphatase (EC 3.1.3.53) ; PPP1R12A protein, human (EC 3.1.3.53)
    Language English
    Publishing date 2019-07-17
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2997-x
    ISSN 1083-351X ; 0021-9258
    ISSN (online) 1083-351X
    ISSN 0021-9258
    DOI 10.1074/jbc.RA118.006075
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Gene therapy in the vasculature and the kidney.

    Ballermann, B J

    Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia

    2000  Volume 20 Suppl 2, Page(s) 19–24

    Abstract: Gene therapy has many potential applications for the treatment of vascular disease. Though a number of tough problems remain to be solved, the potential specificity with which an almost limitless number of mechanisms could be targeted, and the success ... ...

    Abstract Gene therapy has many potential applications for the treatment of vascular disease. Though a number of tough problems remain to be solved, the potential specificity with which an almost limitless number of mechanisms could be targeted, and the success that has been achieved in animal models in vivo make it likely that we will see further rapid expansion of this technology, and therapeutic use of gene therapy in humans in the future.
    MeSH term(s) Genetic Therapy/methods ; Humans ; Kidney Diseases/therapy ; Vascular Diseases/therapy
    Language English
    Publishing date 2000
    Publishing country Spain
    Document type Journal Article ; Review
    ZDB-ID 632512-9
    ISSN 1989-2284 ; 0211-6995
    ISSN (online) 1989-2284
    ISSN 0211-6995
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  6. Article: A role for leptin in glomerulosclerosis?

    Ballermann, B J

    Kidney international

    1999  Volume 56, Issue 3, Page(s) 1154–1155

    MeSH term(s) Animals ; Carrier Proteins/genetics ; Carrier Proteins/physiology ; Diabetic Nephropathies/etiology ; Glomerulosclerosis, Focal Segmental/etiology ; Glomerulosclerosis, Focal Segmental/genetics ; Glomerulosclerosis, Focal Segmental/physiopathology ; Humans ; Leptin ; Proteins/genetics ; Proteins/physiology ; Receptors, Cell Surface ; Receptors, Leptin
    Chemical Substances Carrier Proteins ; LEPR protein, human ; Leptin ; Proteins ; Receptors, Cell Surface ; Receptors, Leptin
    Language English
    Publishing date 1999-09
    Publishing country United States
    Document type Editorial ; Review ; Comment
    ZDB-ID 120573-0
    ISSN 1523-1755 ; 0085-2538
    ISSN (online) 1523-1755
    ISSN 0085-2538
    DOI 10.1046/j.1523-1755.1999.00650.x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Phosphorylation of Rac1 T108 by extracellular signal-regulated kinase in response to epidermal growth factor: a novel mechanism to regulate Rac1 function.

    Tong, Junfeng / Li, Laiji / Ballermann, Barbara / Wang, Zhixiang

    Molecular and cellular biology

    2013  Volume 33, Issue 22, Page(s) 4538–4551

    Abstract: Accumulating evidence has implicated Rho GTPases, including Rac1, in many aspects of cancer development. Recent findings suggest that phosphorylation might further contribute to the tight regulation of Rho GTPases. Interestingly, sequence analysis of ... ...

    Abstract Accumulating evidence has implicated Rho GTPases, including Rac1, in many aspects of cancer development. Recent findings suggest that phosphorylation might further contribute to the tight regulation of Rho GTPases. Interestingly, sequence analysis of Rac1 shows that Rac1 T108 within the (106)PNTP(109) motif is likely an extracellular signal-regulated kinase (ERK) phosphorylation site and that Rac1 also has an ERK docking site, (183)KKRKRKCLLL(192) (D site), at the C terminus. Indeed, we show here that both transfected and endogenous Rac1 interacts with ERK and that this interaction is mediated by its D site. Green fluorescent protein (GFP)-Rac1 is threonine (T) phosphorylated in response to epidermal growth factor (EGF), and EGF-induced Rac1 threonine phosphorylation is dependent on the activation of ERK. Moreover, mutant Rac1 with the mutation of T108 to alanine (A) is not threonine phosphorylated in response to EGF. In vitro ERK kinase assay further shows that pure active ERK phosphorylates purified Rac1 but not mutant Rac1 T108A. We also show that Rac1 T108 phosphorylation decreases Rac1 activity, partially due to inhibiting its interaction with phospholipase C-γ1 (PLC-γ1). T108 phosphorylation targets Rac1 to the nucleus, which isolates Rac1 from other guanine nucleotide exchange factors (GEFs) and hinders Rac1's role in cell migration. We conclude that Rac1 T108 is phosphorylated by ERK in response to EGF, which plays an important role in regulating Rac1.
    MeSH term(s) Active Transport, Cell Nucleus ; Amino Acid Sequence ; Animals ; COS Cells ; Cell Line, Tumor ; Cell Movement ; Chlorocebus aethiops ; Enzyme Activation ; Epidermal Growth Factor/metabolism ; Extracellular Signal-Regulated MAP Kinases/chemistry ; Extracellular Signal-Regulated MAP Kinases/metabolism ; Humans ; Molecular Sequence Data ; Phospholipase C gamma/metabolism ; Phosphorylation ; Protein Interaction Maps ; rac1 GTP-Binding Protein/chemistry ; rac1 GTP-Binding Protein/metabolism
    Chemical Substances Epidermal Growth Factor (62229-50-9) ; Extracellular Signal-Regulated MAP Kinases (EC 2.7.11.24) ; Phospholipase C gamma (EC 3.1.4.3) ; rac1 GTP-Binding Protein (EC 3.6.5.2)
    Language English
    Publishing date 2013-09-16
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 779397-2
    ISSN 1098-5549 ; 0270-7306
    ISSN (online) 1098-5549
    ISSN 0270-7306
    DOI 10.1128/MCB.00822-13
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: Endothelial cell activation.

    Ballermann, B J

    Kidney international

    1998  Volume 53, Issue 6, Page(s) 1810–1826

    MeSH term(s) Endothelium, Vascular/pathology ; Endothelium, Vascular/physiopathology ; Female ; Hemolytic-Uremic Syndrome/pathology ; Hemolytic-Uremic Syndrome/physiopathology ; Humans ; Middle Aged ; Nephritis, Interstitial/pathology ; Nephritis, Interstitial/physiopathology ; Renal Circulation/physiology ; Thrombosis/pathology ; Thrombosis/physiopathology
    Language English
    Publishing date 1998-06
    Publishing country United States
    Document type Case Reports ; Clinical Conference ; Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 120573-0
    ISSN 1523-1755 ; 0085-2538
    ISSN (online) 1523-1755
    ISSN 0085-2538
    DOI 10.1046/j.1523-1755.1998.00943.x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: The insanity defense and mental illness.

    Ballermann, B J

    Science (New York, N.Y.)

    1992  Volume 256, Issue 5055, Page(s) 293

    MeSH term(s) Behavior ; Brain/physiopathology ; Humans ; Mental Disorders/physiopathology
    Language English
    Publishing date 1992-04-17
    Publishing country United States
    Document type Comment ; Letter
    ZDB-ID 128410-1
    ISSN 1095-9203 ; 0036-8075
    ISSN (online) 1095-9203
    ISSN 0036-8075
    DOI 10.1126/science.256.5055.293-a
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  10. Article: Regulation of bovine glomerular endothelial cell growth in vitro.

    Ballermann, B J

    The American journal of physiology

    1989  Volume 256, Issue 1 Pt 1, Page(s) C182–9

    Abstract: To enable the study of glomerular endothelial cell functions and interactions with other glomerular cells, bovine glomerular capillary endothelial cells were established in culture. Selective media were used to facilitate endothelial cell proliferation ... ...

    Abstract To enable the study of glomerular endothelial cell functions and interactions with other glomerular cells, bovine glomerular capillary endothelial cells were established in culture. Selective media were used to facilitate endothelial cell proliferation and to suppress glomerular mesangial cell growth. Glomerular endothelial cells were separated from other cell types by fluorescence-activated cell sorting or, alternatively, by cloning. Glomerular endothelial cells expressed angiotensin I-converting enzyme and factor VIII activity and acetylated LDL uptake, properties generally held to be specific for endothelial cells. Proliferation of subconfluent glomerular endothelial cells was stimulated by basic fibroblast growth factor and, in the presence of heparin sodium, by acidic fibroblast growth factor. Platelet-derived growth factor was without effect on glomerular endothelial cell proliferation. Coculture with mesangial cells markedly inhibited proliferation of subconfluent glomerular endothelial cells. By contrast, medium conditioned by confluent glomerular endothelial cells markedly enhanced proliferation of subconfluent glomerular endothelial cells. These findings suggest that glomerular endothelial cell growth is under autocrine and paracrine control.
    MeSH term(s) Animals ; Carbocyanines ; Cattle ; Cell Division ; Cell Separation ; Cells, Cultured ; Clone Cells/cytology ; Culture Media ; Endocytosis ; Endothelium/cytology ; Fibroblast Growth Factors/pharmacology ; Flow Cytometry ; Fluorescent Dyes ; Glomerular Mesangium/cytology ; Growth Substances/pharmacology ; Heparin/pharmacology ; Hydrogen-Ion Concentration ; Kidney Glomerulus/cytology ; Lipoproteins, LDL/metabolism ; Microscopy, Fluorescence ; Peptidyl-Dipeptidase A/metabolism ; Platelet-Derived Growth Factor/pharmacology
    Chemical Substances Carbocyanines ; Culture Media ; Fluorescent Dyes ; Growth Substances ; Lipoproteins, LDL ; Platelet-Derived Growth Factor ; acetyl-LDL ; 3,3'-dioctadecylindocarbocyanine (40957-95-7) ; Fibroblast Growth Factors (62031-54-3) ; Heparin (9005-49-6) ; Peptidyl-Dipeptidase A (EC 3.4.15.1)
    Language English
    Publishing date 1989-01
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 2948-8
    ISSN 0002-9513
    ISSN 0002-9513
    Database MEDical Literature Analysis and Retrieval System OnLINE

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