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  1. Article ; Online: Investigating ultrastructural morphology in MIRAGE syndrome-derived fibroblasts using transmission electron microscopy.

    Buonocore, Federica / Balys, Monika / Anderson, Glenn / Achermann, John C

    F1000Research

    2024  Volume 12, Page(s) 155

    Abstract: Background: Heterozygous : Methods: We have performed an observational study using transmission electron microscopy (TEM) in a larger number of cells derived from three patients' fibroblasts to assess ultrastructure morphology compared to control ... ...

    Abstract Background: Heterozygous
    Methods: We have performed an observational study using transmission electron microscopy (TEM) in a larger number of cells derived from three patients' fibroblasts to assess ultrastructure morphology compared to control images.
    Results: Consistent changes were observed in cell organelles in all patient samples. In particular, increased endosomal activity was detected, characterised by augmented pinocytosis and vesicle budding, increased endosome number, as well as by large lysosomes and endosomes. Endoplasmic reticulum was also prominent. Mitochondria appeared enlarged in selected cells, possibly due to cellular stress. Cell nuclei did not display major differences compared to controls.
    Conclusions: TEM is a powerful tool to investigate morphological features of tissues and cell organelles, although TEM data could be affected by sample preparation methodology, therefore potentially explaining the variability between independent studies, and its analysis can be dependent on the experience of the researcher. The increased endosomal activity we have observed in patients' fibroblasts could indicate that SAMD9 regulates endocytosis of receptors, acting as an endosome fusion facilitator, or in lysosomal activation. However, the precise mechanism(s) by which SAMD9 regulates cell growth is still not fully understood, and further studies are needed to elucidate its pathogenic pathway and develop therapeutic approaches to support patients.
    MeSH term(s) Humans ; Fibroblasts ; Cell Nucleus ; Endocytosis ; Lysosomes ; Cell Cycle ; Intracellular Signaling Peptides and Proteins
    Chemical Substances SAMD9 protein, human ; Intracellular Signaling Peptides and Proteins
    Language English
    Publishing date 2024-02-13
    Publishing country England
    Document type Observational Study ; Journal Article
    ZDB-ID 2699932-8
    ISSN 2046-1402 ; 2046-1402
    ISSN (online) 2046-1402
    ISSN 2046-1402
    DOI 10.12688/f1000research.129559.2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: A molecular and cellular analysis of human embryonic optic fissure closure related to the eye malformation coloboma.

    Patel, Aara / Anderson, Glenn / Galea, Gabriel L / Balys, Monika / Sowden, Jane C

    Development (Cambridge, England)

    2020  Volume 147, Issue 24

    Abstract: Ocular coloboma is a congenital eye malformation, resulting from a failure in optic fissure closure (OFC) and causing visual impairment. There has been little study of the epithelial fusion process underlying closure in the human embryo and coloboma ... ...

    Abstract Ocular coloboma is a congenital eye malformation, resulting from a failure in optic fissure closure (OFC) and causing visual impairment. There has been little study of the epithelial fusion process underlying closure in the human embryo and coloboma aetiology remains poorly understood. We performed RNAseq of cell populations isolated using laser capture microdissection to identify novel human OFC signature genes and probe the expression profile of known coloboma genes, along with a comparative murine analysis. Gene set enrichment patterns showed conservation between species. Expression of genes involved in epithelial-to-mesenchymal transition was transiently enriched in the human fissure margins during OFC at days 41-44. Electron microscopy and histological analyses showed that cells transiently delaminate at the point of closure, and produce cytoplasmic protrusions, before rearranging to form two continuous epithelial layers. Apoptosis was not observed in the human fissure margins. These analyses support a model of human OFC in which epithelial cells at the fissure margins undergo a transient epithelial-to-mesenchymal-like transition, facilitating cell rearrangement to form a complete optic cup.
    MeSH term(s) Animals ; Apoptosis/genetics ; Base Sequence/genetics ; Coloboma/genetics ; Coloboma/pathology ; Epithelial-Mesenchymal Transition/genetics ; Eye/pathology ; Eye/ultrastructure ; Eye Abnormalities/genetics ; Eye Abnormalities/pathology ; Gene Expression Regulation, Developmental ; Humans ; Laser Capture Microdissection ; Mice ; Microscopy, Electron ; Optic Disk/ultrastructure
    Language English
    Publishing date 2020-12-28
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 90607-4
    ISSN 1477-9129 ; 0950-1991
    ISSN (online) 1477-9129
    ISSN 0950-1991
    DOI 10.1242/dev.193649
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Sirtuin 5 depletion impairs mitochondrial function in human proximal tubular epithelial cells.

    Haschler, Timo N / Horsley, Harry / Balys, Monika / Anderson, Glenn / Taanman, Jan-Willem / Unwin, Robert J / Norman, Jill T

    Scientific reports

    2021  Volume 11, Issue 1, Page(s) 15510

    Abstract: Ischemia is a major cause of kidney damage. Proximal tubular epithelial cells (PTECs) are highly susceptible to ischemic insults that frequently cause acute kidney injury (AKI), a potentially life-threatening condition with high mortality. Accumulating ... ...

    Abstract Ischemia is a major cause of kidney damage. Proximal tubular epithelial cells (PTECs) are highly susceptible to ischemic insults that frequently cause acute kidney injury (AKI), a potentially life-threatening condition with high mortality. Accumulating evidence has identified altered mitochondrial function as a central pathologic feature of AKI. The mitochondrial NAD
    MeSH term(s) Acute Kidney Injury/genetics ; Acute Kidney Injury/metabolism ; Animals ; Blotting, Western ; Cell Line ; Citrate (si)-Synthase/genetics ; Citrate (si)-Synthase/metabolism ; Fluorescent Antibody Technique ; Humans ; Immunohistochemistry ; Male ; Membrane Potential, Mitochondrial/genetics ; Membrane Potential, Mitochondrial/physiology ; Mice ; Mitochondria/genetics ; Mitochondria/metabolism ; Mitophagy/genetics ; Mitophagy/physiology ; Sirtuins/genetics ; Sirtuins/metabolism
    Chemical Substances Citrate (si)-Synthase (EC 2.3.3.1) ; SIRT5 protein, human (EC 3.5.1.-) ; Sirtuins (EC 3.5.1.-)
    Language English
    Publishing date 2021-07-30
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-021-94185-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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