Novel mitochondrial derived Nuclear Excisosome degrades nuclei during differentiation of prosimian Galago (bush baby) monkey lenses.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 03 06 2020
accepted: 16 10 2020
entrez: 12 11 2020
pubmed: 13 11 2020
medline: 23 12 2020
Statut: epublish

Résumé

The unique cellular organization and transparent function of the ocular lens depend on the continuous differentiation of immature epithelial cells on the lens anterior surface into mature elongated fiber cells within the lens core. A ubiquitous event during lens differentiation is the complete elimination of organelles required for mature lens fiber cell structure and transparency. Distinct pathways have been identified to mediate the elimination of non-nuclear organelles and nuclei. Recently, we reported the discovery of a unique structure in developing fiber cells of the chick embryo lens, called the Nuclear Excisosome, that is intractably associated with degrading nuclei during lens fiber cell differentiation. In the chick lens, the Nuclear Excisosome is derived from projections of adjacent cells contacting the nuclear envelope during nuclear elimination. Here, we demonstrate that, in contrast to the avian model, Nuclear Excisosomes in a primate model, Galago (bush baby) monkeys, are derived through the recruitment of mitochondria to form unique linear assemblies that define a novel primate Nuclear Excisosome. Four lenses from three monkeys aged 2-5 years were fixed in formalin, followed by paraformaldehyde, then processed for Airyscan confocal microscopy or transmission electron microscopy. For confocal imaging, fluorescent dyes labelled membranes, carbohydrate in the extracellular space, filamentous actin and nuclei. Fiber cells from Galago lenses typically displayed prominent linear structures within the cytoplasm with a distinctive cross-section of four membranes and lengths up to 30 μm. The outer membranes of these linear structures were observed to attach to the outer nuclear envelope membrane to initiate degradation near the organelle-free zone. The origin of these unique structures was mitochondria in the equatorial epithelium (not from plasma membranes of adjacent cells as in the chick embryo model). Early changes in mitochondria appeared to be the collapse of the cristae and modification of one side of the mitochondrial outer membrane to promote accumulation of protein in a dense cluster. As a mitochondrion surrounded the dense protein cluster, an outer mitochondrial membrane enclosed the protein to form a core and another outer mitochondrial membrane formed the outermost layer. The paired membranes of irregular texture between the inner core membrane and the outer limiting membrane appeared to be derived from modified mitochondrial cristae. Several mitochondria were involved in the formation and maturation of these unique complexes that apparently migrated around the fulcrum into the cytoplasm of nascent fiber cells where they were stabilized until the nuclear degradation was initiated. Thus, unlike in the chick embryo, the Galago lenses degraded nuclear envelopes with a Nuclear Excisosome derived from multiple mitochondria in the epithelium that formed novel linear assemblies in developing fiber cells. These findings suggest that recruitment of distinct structures is required for Nuclear Excisosome formation in different species.

Identifiants

pubmed: 33180800
doi: 10.1371/journal.pone.0241631
pii: PONE-D-20-16891
pmc: PMC7660580
doi:

Substances chimiques

Actins 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0241631

Subventions

Organisme : NEI NIH HHS
ID : R01 EY008148
Pays : United States
Organisme : NEI NIH HHS
ID : R01 EY029708
Pays : United States
Organisme : NEI NIH HHS
ID : R01 EY013462
Pays : United States

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

M Joseph Costello (MJ)

Department of Cell Biology and Physiology, University of North Carolina, Chapel Hill, NC, United States of America.

Kurt O Gilliland (KO)

Department of Cell Biology and Physiology, University of North Carolina, Chapel Hill, NC, United States of America.

Ashik Mohamed (A)

Ophthalmic Biophysics, L V Prasad Eye Institute, Hyderabad, Telangana, India.

Kevin L Schey (KL)

Biochemistry Department, Vanderbilt University, Nashville, TN, United States of America.

Sönke Johnsen (S)

Biology Department, Duke University, Durham, NC, United States of America.

Lisa A Brennan (LA)

Department of Biomedical Science, Florida Atlantic University, Boca Raton, FL, United States of America.

Marc Kantorow (M)

Department of Biomedical Science, Florida Atlantic University, Boca Raton, FL, United States of America.

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Classifications MeSH