Imaging the endothelial glycocalyx in vitro by rapid freezing/freeze substitution transmission electron microscopy

Eno E. Ebong, Frank P. Macaluso, David C. Spray, John M. Tarbell

Research output: Contribution to journalArticle

101 Citations (Scopus)

Abstract

Objective-: Recent publications questioned the validity of endothelial cell (EC) culture studies of glycocalyx (GCX) function because of findings that GCX in vitro may be substantially thinner than GCX in vivo. The assessment of thickness differences is complicated by GCX collapse during dehydration for traditional electron microscopy. We measured in vitro GCX thickness using rapid freezing/freeze substitution (RF/FS) transmission electron microscopy (TEM), taking advantage of the high spatial resolution provided by TEM and the capability to stably preserve the GCX in its hydrated configuration by RF/FS. Methods and results-: Bovine aortic EC (BAEC) and rat fat pad EC were subjected to conventional or RF/FS-TEM. Conventionally preserved BAEC GCX was 0.040 μm in thickness. RF/FS-TEM revealed impressively thick BAEC GCX of-11 μm and rat fat pad EC GCX of-5 μm. RF/FS-TEM also discerned GCX structure and thickness variations due to heparinase III enzyme treatment and extracellular protein removal, respectively. Immunoconfocal studies confirmed that the in vitro GCX is several micrometers thick and is composed of extensive and well-integrated heparan sulfate, hyaluronic acid, and protein layers. Conclusion-: New observations by RF/FS-TEM reveal substantial GCX layers on cultured EC, supporting their continued use for fundamental studies of GCX and its function in the vasculature.

Original languageEnglish (US)
Pages (from-to)1908-1915
Number of pages8
JournalArteriosclerosis, Thrombosis, and Vascular Biology
Volume31
Issue number8
DOIs
StatePublished - Aug 2011

Fingerprint

Freeze Substitution
Glycocalyx
Transmission Electron Microscopy
Freezing
Endothelial Cells
heparitinsulfate lyase
In Vitro Techniques
Adipose Tissue
Heparitin Sulfate
Hyaluronic Acid
Dehydration

Keywords

  • confocal microscopy
  • endothelium
  • glycocalyx
  • rapid freezing/freeze substitution
  • transmission electron microscopy

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

Cite this

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title = "Imaging the endothelial glycocalyx in vitro by rapid freezing/freeze substitution transmission electron microscopy",
abstract = "Objective-: Recent publications questioned the validity of endothelial cell (EC) culture studies of glycocalyx (GCX) function because of findings that GCX in vitro may be substantially thinner than GCX in vivo. The assessment of thickness differences is complicated by GCX collapse during dehydration for traditional electron microscopy. We measured in vitro GCX thickness using rapid freezing/freeze substitution (RF/FS) transmission electron microscopy (TEM), taking advantage of the high spatial resolution provided by TEM and the capability to stably preserve the GCX in its hydrated configuration by RF/FS. Methods and results-: Bovine aortic EC (BAEC) and rat fat pad EC were subjected to conventional or RF/FS-TEM. Conventionally preserved BAEC GCX was 0.040 μm in thickness. RF/FS-TEM revealed impressively thick BAEC GCX of-11 μm and rat fat pad EC GCX of-5 μm. RF/FS-TEM also discerned GCX structure and thickness variations due to heparinase III enzyme treatment and extracellular protein removal, respectively. Immunoconfocal studies confirmed that the in vitro GCX is several micrometers thick and is composed of extensive and well-integrated heparan sulfate, hyaluronic acid, and protein layers. Conclusion-: New observations by RF/FS-TEM reveal substantial GCX layers on cultured EC, supporting their continued use for fundamental studies of GCX and its function in the vasculature.",
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author = "Ebong, {Eno E.} and Macaluso, {Frank P.} and Spray, {David C.} and Tarbell, {John M.}",
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AU - Ebong, Eno E.

AU - Macaluso, Frank P.

AU - Spray, David C.

AU - Tarbell, John M.

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N2 - Objective-: Recent publications questioned the validity of endothelial cell (EC) culture studies of glycocalyx (GCX) function because of findings that GCX in vitro may be substantially thinner than GCX in vivo. The assessment of thickness differences is complicated by GCX collapse during dehydration for traditional electron microscopy. We measured in vitro GCX thickness using rapid freezing/freeze substitution (RF/FS) transmission electron microscopy (TEM), taking advantage of the high spatial resolution provided by TEM and the capability to stably preserve the GCX in its hydrated configuration by RF/FS. Methods and results-: Bovine aortic EC (BAEC) and rat fat pad EC were subjected to conventional or RF/FS-TEM. Conventionally preserved BAEC GCX was 0.040 μm in thickness. RF/FS-TEM revealed impressively thick BAEC GCX of-11 μm and rat fat pad EC GCX of-5 μm. RF/FS-TEM also discerned GCX structure and thickness variations due to heparinase III enzyme treatment and extracellular protein removal, respectively. Immunoconfocal studies confirmed that the in vitro GCX is several micrometers thick and is composed of extensive and well-integrated heparan sulfate, hyaluronic acid, and protein layers. Conclusion-: New observations by RF/FS-TEM reveal substantial GCX layers on cultured EC, supporting their continued use for fundamental studies of GCX and its function in the vasculature.

AB - Objective-: Recent publications questioned the validity of endothelial cell (EC) culture studies of glycocalyx (GCX) function because of findings that GCX in vitro may be substantially thinner than GCX in vivo. The assessment of thickness differences is complicated by GCX collapse during dehydration for traditional electron microscopy. We measured in vitro GCX thickness using rapid freezing/freeze substitution (RF/FS) transmission electron microscopy (TEM), taking advantage of the high spatial resolution provided by TEM and the capability to stably preserve the GCX in its hydrated configuration by RF/FS. Methods and results-: Bovine aortic EC (BAEC) and rat fat pad EC were subjected to conventional or RF/FS-TEM. Conventionally preserved BAEC GCX was 0.040 μm in thickness. RF/FS-TEM revealed impressively thick BAEC GCX of-11 μm and rat fat pad EC GCX of-5 μm. RF/FS-TEM also discerned GCX structure and thickness variations due to heparinase III enzyme treatment and extracellular protein removal, respectively. Immunoconfocal studies confirmed that the in vitro GCX is several micrometers thick and is composed of extensive and well-integrated heparan sulfate, hyaluronic acid, and protein layers. Conclusion-: New observations by RF/FS-TEM reveal substantial GCX layers on cultured EC, supporting their continued use for fundamental studies of GCX and its function in the vasculature.

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