Organisms and the tissues that constitute them, are fundamentally affected by a variety of intrinsic aberrations (e.g. gene dysfunctions) and extrinsic insults (e.g. infections). Histopathology enables insightful evaluation of the morphological manifestations of functional disturbances (e.g. aberrant gene expression).
The HistoPathology (HP) facility provides unique, combined expertise in histological techniques and comparative pathology to provide comprehensive tissue analyses. Our services encompass tissue processing, routine histological stains, a growing array of immunostaining techniques and in situ hybridization methods, and are delivered in highly individualized approaches for each project.
Do you work with tissue systems or animal models? Do you study disease processes? Are you interested in our services?
We can assist with study design, and development and implementation of protocols for standard as well as customized experimental studies.
We routinely provide services and support for:
- Sample collection, fixation, and processing
- Cryo- and paraffin embedding and sectioning
We have experience working with several types of samples including whole organisms, isolated organs, slices or groups of tissues, cell cultures (2D and 3D), fluids, and inorganic materials.
We perform routine and special histochemical stains along with immunostainings (immunofluorescence, immunohistochemistry, and multiplex stains). We have experience with background reduction in problematic “mouse on mouse” stainings as well as cross-reactivity avoidance during multiplex stainings. We also offer RNA in situ hybridization with basic protocols and RNAscope.
Our facility features in-house comparative pathology expertise for the evaluation of processing outcomes, analysis of morphological features and lesional parameters, and integration of the results of processing and analysis into manuscripts, presentations, or other pertinent documents. Pathology services offered by the VBCF HistoPathology facility include:
- Consultations and reviews
- Microscopic analyses of morphological features
- Representative imaging and documentation
- Digital quantification (in collaboration with IMP Biooptics facility)
- Manuscript support
Support during self-service is offered exclusively to IMP/IMBA/GMI members. It includes training in the use of all the sectioning equipment available in the facility and troubleshooting support.
Secondary and inter-facility support includes coordinated processing services (e.g., perfusion and dissection after in vivo imaging) offered with other facilities for multimodal projects. For example, HistoPathology staff work collaboratively with the IMP Biooptics core facility to facilitate whole slide digitization (slide scanning).
Correlative interpretation and validation of histomorphologic findings in relation to information obtained from other modalities is offered as part of pathology services.
A fully automated immunostainer with the capacity for 30 slides per run. It can perform immunochemistry staining with either DAB or AP-red detection systems in as little as 3 h and allows for high reproducibility.
If you are interested in having immunostains done on your samples with the Leica Bond III, please contact us.
This instrument performs automatic tissue dehydration, clearing, and paraffin infiltration. The LOGOS dehydrator competes in quality, versatility, and safety with other dehydrators on the market. It can perform 210 tissue blocks per run, with any kind of tissue up to 6 mm in thickness.
If you are interested in using the LOGOS, please contact us.
Microtome to section frozen or cryo-embedded tissues. Open-top cryostat with ergonomic design for working while standing or sitting. This cryostat allows a section thickness range from 0.5 to 100 µm. The temperature for the specimen clumper is controlled and ranges from 10°C to -35°C. There is a separate temperature control for the knife carrier down to -35°C.
To order a service, please contact the facility staff as early as possible to discuss relevant details and agree upon timelines. When submitting samples, please remember to label each sample with a unique identifier (e.g., mouse ID or organoid batch number), submitter initials, and date. Please also provide relevant details such as: genotype, treatment, or other procedure.I f procedures relevant to coordinated processing have been performed (e.g. in vivo imaging), please ensure that pertinent details and representative images are provided. The clearer and more complete the information provided, the lower the risk of downstream errors. The facility can also provide you with submission forms for your projects.
IMP, IMBA, and GMI researchers can, by themselves, use all sectioning equipment in the facility, but only after attending a training session with our staff. To set up an appointment for training, please contact the facility staff.
In addition, the facility offers many for-fee-services to members of the Vienna BioCenter (academic institutions and companies) as well as external academic institutions and private companies.
For paid service projects, the users from the Vienna BioCenter have priority. Otherwise, the service projects are performed in the order they are requested; ‘first come, first served’.
We require acknowledgement of facility use in publications.
A simple statement is sufficient and can be placed in the Materials and Methods section or in the Acknowledgments section, depending on the journal format.
The XXXXXX was performed by the Histopathology Facility
at Vienna BioCenter Core Facilities (VBCF), member of the Vienna BioCenter (VBC), Austria.
In case of (co-)authorship:
The Vienna BioCenter Core Facilities (VBCF) Histopathology Facility acknowledges funding from the Austrian Federal Ministry of Education, Science & Research; and the City of Vienna.
Uribesalgo I, Hoffmann D, Zhang Y, Kavirayani A, Lazovic J, Berta J, Novatchkova M, Pai TP, Wimmer RA, László V, Schramek D, Karim R, Tortola L, Deswal S, Haas L, Zuber J, Szűcs M, Kuba M., Dome B, Cao Y, Haubner BJ, Penninger JM. EMBO Mol Med. 2019 Aug; 11(8)
Nagy V, Hollstein R, Pai TP, Herde MK, Buphamalai P, Moeseneder P, Lenartowicz E, Kavirayani A, Korenke GC, Kozieradzki I, Nitsch R, Cicvaric A, Monje Quiroga FJ, Deardorff MA, Bedoukian EC, Li Y, Yigit G, Menche J, Perçin EF, Wollnik B, Henneberger C, Kaiser FJ, Penninger JM, Neurol Genet Jun 2019, 5 (3) e330
Uras IZ, Maurer B, Nivarthi H, Jodl P, Kollmann K, Prchal-Murphy M, Milosevic Feenstra JD, Zojer M, Lagger S, Grausenburger R, Grabner B, Holly R, Kavirayani A, Bock C, Gisslinger H, Valent P, Kralovics R, Sexl V, Blood. 2019 Apr; 133(15)
Bönelt P, Wöhner M, Minnich M, Tagoh H, Fischer M, Jaritz M, Kavirayani A, Garimella M, Karlsson MCI, Busslinger M. EMBO J. 2019 Jan; 38(2).
Ivin M, Dumigan A, de Vasconcelos FN, Ebner F, Borroni M, Kavirayani A, Przybyszewska KN, Ingram RJ, Lienenklaus S, Kalinke U, Stoiber D, Bengoechea JA, Kovarik P, PLoS Pathog. 2017 Nov; 13(11): e1006696.
Asaoka T, Almagro J, Ehrhardt C, Tsai I, Schleiffer A, Deszcz L, Junttila S, Ringrose L, Mechtler K, Kavirayani A, Gyenesei A, Hofmann K, Duchek P, Rittinger K, Ikeda F, EMBO Rep. 2016 Nov; 17(11): 1624-1640.
Wirnsberger G, Zwolanek F, Asaoka T, Kozieradzki I, Tortola L, Wimmer RA, Kavirayani A, Fresser F, Baier G, Langdon WY, Ikeda F, Kuchler K, Penninger JM, Nat Med. 2016 Aug; 22(8): 915-923
Sigl V, Owusu-Boaitey K, Joshi PA, Kavirayani A, Wirnsberger G, Novatchkova M, Kozieradzki I, Schramek D, Edokobi N, Hersl J, Sampson A, Odai-Afotey A, Lazaro C, Gonzalez-Suarez E, Pujana MA, Cimba F, Heyn H, Vidal E, Cruickshank J, Berman H, Sarao R, Ticevic M, Uribesalgo I, Tortola L, Rao S, Tan Y, Pfeiler G, Lee EY, Bago-Horvath Z, Kenner L, Popper H, Singer C, Khokha R, Jones LP, Penninger JM, Cell Res. 2016 Jul; 26(7): 761-774.
A simple and robust protocol for immunostaining Arabidopsis pollen nuclei.
Borg M, Buendía D, Berger F, Plant Reproduction. 2019 Jan; doi.org/10.1007/s00497-018-00360-7
Human blood vessel organoids as a model of diabetic vasculopathy.
Wimmer RA, Leopoldi A, Aichinger M, Wick N, Hantusch B, Novatchkova M, Taubenschmid J, Hämmerle M, Esk C, Bagley JA, Lindenhofer D, Chen G, Boehm M, Agu CA, Yang F, Fu B, Zuber J, Knoblich JA, Kerjaschki D, Penninger JM, Nature 2019 Jan;565(7740):505-510
Central amygdala circuit dynamics underlying the benzodiazepine anxiolytic effect.
Griessner J, Pasieka M, Böhm V, Grössl F, Kaczanowska J, Pliota P, Kargl D, Werner B, Kaouane N, Strobelt S, Kreitz S, Hess A, Haubensak W, Mol Psychiatry. 2018 Nov 30
Single-cell analysis uncovers convergence of cell identities during axolotl limb regeneration.
Gerber T, Murawala P, Knapp D, Masselink W, Schuez M, Hermann S, Gac-Santel M, Nowoshilow S, Kageyama J, Khattak S, Currie JD, Camp JG, Tanaka EM, Treutlein B, Science, 2018 Oct; 362 (6413): eaaq0681
Dorsal tegmental dopamine neurons gate associative learning of fear.
Groessl F, Munsch T, Meis S, Griessner J, Kaczanowska J, Pliota P, Kargl D, Badurek S, Kraitsy K, Rassoulpour A, Zuber J, Lessmann V, Haubensak W, Nat. Neurosci 2018 Jul;21(7):952-62
The axolotl genome and the evolution of key tissue formation regulators.
Nowoshilow S, Schloissnig S, Fei JF, Dahl A, Pang AWC, Pippel M, Winkler S, Hastie AR, Young G, Roscito JG, Falcon F, Knapp D, Powell S, Cruz A, Cao H, Habermann B, Hiller M, Tanaka EM, Myers EW, Nature, 2018 Feb; 554: 50-55
RANK rewires energy homeostasis in lung cancer cells and drives primary lung cancer.
Rao S, Sigl V, Wimmer RA, Novatchkova M, Jais A, Wagner G, Handschuh S, Uribesalgo I, Hagelkruys A, Kozieradzki I, Tortola L, Nitsch R, Cronin SJ, Orthofer M, Branstetter D, Canon J, Rossi J, D'Arcangelo M, Botling J, Micke P, Fleur L, Edlund K, Bergqvist M, EkmanS, Lendl T, Popper H, Takayanagi H, Kenner L, Hirsch FR, Dougall W, Penninger JM, Genes Dev. 2017 Oct; 31(20): 2099-2112
BET-Bromodomain Inhibitors Engage the Host Immune System and Regulate Expression of the Immune Checkpoint Ligand PD-L1.
Hogg SJ, Vervoort SJ, Deswal S, Ott CJ, Li J, Cluse LA, Beavis PA, Darcy PK, Martin BP, Spencer A, Traunbauer AK, Sadovnik I, Bauer K, Valent P, Bradner JE, Zuber J, Shortt J, Johnstone RW, Cell Rep. 2017 Feb; 18(9): 2162-2174
Fast volumetric calcium imaging across multiple cortical layers using sculpted light.
Prevedel R, Verhoef AJ, Pernía-Andrade AJ, Weisenburger S, Huang BS, Nöbauer T, Fernández A, Delcour JE, Golshani P, Baltuska A, Vaziri A, Nat Methods, 2016 Dec; 13(12): 1021-1028