Department für Anatomie, Histologie und Embryologie

debbage-figure11Working Group for Endothelial Biology

Endothelial biology is at the focus of this group’s research.

Several of our projects are grouped around the biology of blood vessels in tumours (Figures 1, 2).

debbage-figure01 Figure 1: Electron microscope image of a small blood vessel (capillary)
debbage-figure02 Figure 2: Breast carcinoma tumour cell undergoing mitosis (electron microscope image)

The interactions between endothelial cells and other cell types lie at the heart of the immune response, determine the ability of tumour cells to proliferate and to form metastases, and – last but not least – sculpt the various organs and mediate organ functions.

Pathophysiologies of the vascular system are involved in inflammatory conditions, in tumour growth and spread, and in cardiovascular diseases. Reflecting this, our group collaborates actively with several clinics at the University of Innsbruck, and also internationally with institutes and clinics elsewhere in Europe. In 1998 we presented a technique for intravital lectin perfusion (Debbage et al., 1998) which permits correlative fluorescence and electron microscopical analyses of microvessel density and microvessel permeability (Figures 3,4). In collaboration with the GSF Institutes of Radiobiology (Dr. J. Griebel) and Pathology (Dr. P. Hutzler), and with the Clinic for Radiotherapy and Radio-Oncology (Dr. A. DeVries) at the University of Innsbruck, we showed that fractionated radiotherapy leads to long-standing hyperpermeability of the blood vessels, and also to significant reduction in their density (Figures 3,4). This work formed the basis for successful completion of a doctoral thesis by Dr. Sonja Seidl (2001). Questions arising from that project led to subsequent projects aimed at understanding deeper aspects of endothelial biology.

The group has received funding: Swarovski Foundation, National Bank of Austria, Project 9273.

In the following we introduce here some of our ongoing projects grouped around endothelial cell biology:

debagge-figures03-04
Figure 3,4: Tumour blood vessels, no radiation therapy (3, at left) and after radiation therapy (4, at right)

1. Endothelial cell biology in tumours: ultrastructural analysis of endothelial cell interactions with prostate tumour cells

Question:
How does blood vessel growth relate to metastasis? See Figure 5.
Collaborations:
  • Clinic for Urology, (University of Innsbruck), with Professor G. Bartsch
  • Institute of Pathology, (University of Innsbruck), with Professor H. Rogatsch

debagge-figure05 Figure 5: Angiogenesis in a prostate carcinoma (electron micrograph, mosaic image)

seeber-and-wieser
Julia Seeber Elisabeth Wieser
Doctoral students carrying out this research:
  • Miss Elisabeth Wieser (cand. med., Univ. Innsbruck);
  • Miss Julia Seeber (cand. med., Univ. Innsbruck).
Presentations:
  • At the XVII Congress EAU in Birmingham, March 2002 (Strohmeyer et al., 2002)
  • At the 43rd Meeting of the Society for Histochemistry, Vienna, September 2001.


 

2. Endothelial cell biology in tumours: ultrastructural analysis of endothelial interactions with tumour cells in breast cancers Question: How do the tumour cells penetrate blood vessels during metastasis? See Figure 6.

Collaborations:
  • Clinic for General Surgery, (University of Innsbruck) with Dr. M. Dünser
  • Clinic for Radiology, (University of Innsbruck) with Professor W. Jaschke and Professor W. Buchberger
  • Institute of Pathology (University of Innsbruck with Dr. P. Obrist.

debbage-figure06 Figure 6: A migrating tumour cell in a breast carcinoma (electron microscope image)

silvia-dobler dobler-and-debbage
Silvia Dobler Silvia Dobler with Paul Debbage
Doctoral student carrying out this research:
  • Miss Silvia Dobler (cand. med., Univ. Innsbruck).


 

3. Endothelial cell biology in tumours: ultrastructural analysis of radiation effects on blood vessels in a human glioblastoma ectopically implanted in the nude mouse

Question 1:
What are the mechanisms of the tumour-endothelial interactions? Tumor-induced growth of small blood vessels is often seen (Figure 7).
Question 2:
What are the effects of small radiation doses on the endothelial cells, and on the tumour-endothelial interactions?
Collaborations:
  • Department of Radiation Oncology, University Medical Centre Nijmegen, The Netherlands, with Professor A. van der Kogel
  • Institute for Pathology of the GSF Research Centre in Munich (Germany),with Dr. P. Hutzler

debbage-figure07 Figure 7: Angiogenesis in E106 glioblastoma

eveline-meier
Eveline Meier
Doctoral student carrying out this research:
Miss Eveline Meier (cand. med., Univ. Innsbruck).
Presentations:
  • At the 43rd Meeting of the Society for Histochemistry, Vienna, September 2001


 

4. Endothelial cell biology in normal tissues: Development of a model system for analysis of radiation effects on human tissues

Question:
Can we establish organ-type culture of human tissues which can be used to analyse radiation effects on human blood vessels. Early work on this model began with umbilical vein endothelia (Debbage et al., 2000). Present work focuses on fetal microvessels in the human placental cotyledon (Figure 8).
Collaborations:
  • Clinic for Gynaecology and Obstetrics (University of Innsbruck), with Professor C. Marth and Dr. E. Sölder
  • Clinic for Radiology I (University of Innsbruck), with Professor W. Jaschke, Professor W. Buchberger and Dr. C. Kremser
  • Clinic for Radiotherapy and Radio-Oncology (University of Innsbruck), with Professor P. Lukas
  • Institute of Pathology (University of Innsbruck), with Dr. A. Kreczy

debbage-figure08 Figure 8: Wall of placental villus (electron micrograph)
Doctoral student carrying out this research:
  • Miss Isabella Höliner (cand. med, Univ. Innsbruck).
Funded by
the Swarovski Foundation.
Presentation:
  • At the 42nd Meeting of the Society for Histochemistry, Les Diablerets, Switzerland.

5. Development of vascular markers for use in Magnetic Resonance Imaging

Collaborations:
  • Clinic for Radiology I at the University of Innsbruck,
  • Institute for Anorganic Chemistry at the University of Vienna.

irena-paschkunova
Isabella Höliner with Paul Debbage Irena Paschkunova
Doctoral students carrying out this research:
  • Miss Isabella Höliner (cand. med, Univ. Innsbruck);
  • Miss Irena Paschkunova (Univ. Vienna).
Funded by
  • the National Bank of Austria, Project 9273.


 

Other Work

kunz-and-mistlberger
Karoline Kunz Klaudia Mistlberger

Other work of a technical nature aims to provide new methods of viewing endothelial cells, particularly by use of low voltage scanning electron microscopy. This work is in preparation for publication and formed the basis for the doctoral thesis submitted May 2002 by Miss Karoline Kunz.
Ongoing work is being carried out by Miss Klaudia Mistlberger as part of her doctoral thesis.


debbage-figure09 Figure 9: LVSEM IMAGE of microvilli

Occasional collaborations

This group collaborates on an occasional basis with neighbouring research groups at the University of Innsbruck, particularly when the skills available to us complement those of our colleagues in neighbouring institutions. For example, we recently worked with the group of Dr. H. Talasz (Institute for Medical Chemistry, University of Innsbruck) to illustrate the ultrastructure of apoptotic cells (Talasz et al., 2002). We also investigated bone development by immunohistochemical techniques, in collaboration with Professor Dr. H. Fritsch (Institute for Anatomy and Histology, University of Innsbruck) (Fritsch et al., 2001). We collaborated with Professor Michael Hess to demonstrate myelin chemistry in the glacier mummy “Ötzi” (Hess et al., 1998). We have collaborated with Professor Dr. M. Pavelka to visualise endocytotic processes by use of electron histochemical techniques (Hess et al., 2000; Pavelka et al., 1998).

Technical colleagues

julianna-forgo
Julianna Forgo
  • Mrs. Julianna Forgo,
  • Mr. Rudolf Haring.


 

Selected citations (primary literature)

  • Debbage, Pl; Griebel, J; Ried, M; Gneiting, T; DeVries, A; Hutzler, P (1998) Lectin intravital perfusion studies in tumor-bearing mice: micrometer-resolution, wide-area mapping of microvascular labeling, distinguishing efficiently and inefficiently perfused microregions in the tumor. J Histochem Cytochem. 46:627-39
  • Debbage PL, Seidl S, Kreczy A, Hutzler P, Pavelka M & Lukas P (2000) Vascular permeability and hyperpermeability in a murine adenocarcinoma after fractionated radiotherapy: an ultrastructural tracer study. Histochem. Cell Biol. 114: 259-275
  • Debbage PL, Sölder E, Seidl S, Hutzler P, Hugl B, Öfner D & Kreczy A (2001) Intravital lectin perfusion analysis of vascular permeability in human micro- and macro- blood vessels. Histochem. Cell Biol. 116: 349-359
  • Fritsch H, Brenner E & Debbage P (2001) Ossification in the human calcaneus: a model for spatial bone development and ossification. J Anat. 199: 609-16
  • Hess MW, Kirschning E, Pfaller K, Debbage Pl, Hohenberg H & Klima G (1998) 5000-year-old myelin: uniquely intact in molecular configuration and fine structure. Curr. Biol. 8: R512-3
  • Hess MW, Muller M, Debbage Pl, Vetterlein M & Pavelka M (2000( Cryopreparation provides new insight into effects of brefeldin ! on the structure of the HepG2 Golgi apparatus. J. Struct. Biol. 130: 63-72
  • Pavelka M, Ellinger A, Debbage P, Loewe C, Vetterlein M & Roth J (1998) Endocytic routes to the Golgi apparatus. Histochem. Cell Biol. 109: 555-70
  • Strohmeyer et al. (2002) Birmingham meeting xxxxxxxxx
  • Talasz H, Helliger W, Sarg B, Debbage PL, Puschendorf B & Lindner H (2002) Hyperphosphorylation of histone H2A.X and dephosphorylation of histone H1 subtypes in the course of apoptosis. Cell Death Differ. 9: 27-39

Doctoral theses

  • Seidl S (2001) Doctoral thesis, Medical Faculty of the University of Innsbruck: Vaskuläre Veränderungen in AT17-Tumoren der Maus während Strahlentherapie
  • Kunz K (2002) Doctoral thesis, Medical Faculty of the University of Innsbruck: Low voltage scanning electron microscopic analysis of epithelial cell surfaces: characterisation of a carbohydrate rich surface layer.

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