dc.contributor.author
Kraus, Annalena
dc.contributor.author
Rose, Victoria
dc.contributor.author
Krüger, René
dc.contributor.author
Sarau, George
dc.contributor.author
Kling, Lasse
dc.contributor.author
Schiffer, Mario
dc.contributor.author
Christiansen, Silke H.
dc.contributor.author
Müller-Deile, Janina
dc.date.accessioned
2024-03-01T12:40:59Z
dc.date.available
2024-03-01T12:40:59Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/42518
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-42243
dc.description.abstract
Podocytes are critical components of the glomerular filtration barrier, sitting on the outside of the glomerular basement membrane. Primary and secondary foot processes are characteristic for podocytes, but cell processes that develop in culture were not studied much in the past. Moreover, protocols for diverse visualization methods mostly can only be used for one technique, due to differences in fixation, drying and handling. However, we detected by single-cell RNA sequencing (scRNAseq) analysis that cells reveal high variability in genes involved in cell type-specific morphology, even within one cell culture dish, highlighting the need for a compatible protocol that allows measuring the same cell with different methods. Here, we developed a new serial and correlative approach by using a combination of a wide variety of microscopic and spectroscopic techniques in the same cell for a better understanding of podocyte morphology. In detail, the protocol allowed for the sequential analysis of identical cells with light microscopy (LM), Raman spectroscopy, scanning electron microscopy (SEM) and atomic force microscopy (AFM). Skipping the fixation and drying process, the protocol was also compatible with scanning ion-conductance microscopy (SICM), allowing the determination of podocyte surface topography of nanometer-range in living cells. With the help of nanoGPS Oxyo®, tracking concordant regions of interest of untreated podocytes and podocytes stressed with TGF-β were analyzed with LM, SEM, Raman spectroscopy, AFM and SICM, and revealed significant morphological alterations, including retraction of podocyte process, changes in cell surface morphology and loss of cell-cell contacts, as well as variations in lipid and protein content in TGF-β treated cells. The combination of these consecutive techniques on the same cells provides a comprehensive understanding of podocyte morphology. Additionally, the results can also be used to train automated intelligence networks to predict various outcomes related to podocyte injury in the future.
en
dc.format.extent
19 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
single-cell RNA sequencing
en
dc.subject
podocytes; foot processes
en
dc.subject
light microscopy
en
dc.subject
Raman spectroscopy
en
dc.subject
scanning electron microscopy
en
dc.subject
atomic force microscopy
en
dc.subject
scanning ion-conductance microscopy
en
dc.subject
nanoGPS tracking
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::530 Physik::530 Physik
dc.title
Characterizing Intraindividual Podocyte Morphology In Vitro with Different Innovative Microscopic and Spectroscopic Techniques
dc.type
Wissenschaftlicher Artikel
dc.identifier.sepid
97173
dcterms.bibliographicCitation.articlenumber
1245
dcterms.bibliographicCitation.doi
10.3390/cells12091245
dcterms.bibliographicCitation.journaltitle
Cells
dcterms.bibliographicCitation.number
9
dcterms.bibliographicCitation.originalpublishername
MDPI
dcterms.bibliographicCitation.originalpublisherplace
Basel
dcterms.bibliographicCitation.volume
12 (2023)
dcterms.bibliographicCitation.url
https://www.mdpi.com/2073-4409/12/9/1245
refubium.affiliation
Physik
refubium.affiliation.other
Institut für Experimentalphysik
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
2073-4409