Der Jahresbericht 2025 wurde an der Stiftungsratssitzung vom 25. Juni 2026 einstimmig genehmigt. Er kann hier heruntergeladen werden. Der Jahresbericht 2026 erscheint im Juli 2027.
The annual report 2025 has been approved by the board of the Foundation at its meeting of June 25, 2026. It can be downloaded here (German). The annual report 2026 will be published in July 2027.
Our research focuses on understanding the mechanisms underlying dental caries and erosive tooth wear, with particular interest in the role of oral biofilms and novel biofilm management strategies. In recent years, our group has investigated the potential of natural compounds, such as polyphenols, to modulate oral biofilms and the salivary pellicle, with the aim of developing new preventive strategies against caries and dental erosion.
With the support of the the UniBern Forschungsstiftung via the BEKB Förderfonds funding pool, we acquired new laboratory infrastructure that enables advanced molecular investigations of dental biofilms, saliva, and acquired enamel pellicle components for both in vitro and clinical studies.
The devices – an automated colony counter for optimized biofilm quantification (Figure 1A), an OD600 photometer for inoculum standardization (Figure 1B), a thermoshaker for molecular biology applications with exchangeable block (Figure 1C) and a cooling high-speed centrifuge (Figure 1C) – support investigations of novel antimicrobial compounds, as well as sample preparation for PCR-based analyses, oral microbiome sequencing, and proteomics, to study the oral biofilm composition, virulence, and interactions with dental tissues.
Dr. Luciana Pisenti Berto
Prof. Dr. Thiago Saads Carvalho
Klinik für Zahnerhaltung, Präventiv- und Kinderzahnmedizin
Die Projektförderung wurde ermöglicht durch einen Beitrag desBEKB Förderfonds
Figure 1. Acquired devices. (A) Automated colony counter. (B) OD600 photometer. (C) Thermoshaker with exchangeable block and cooling high-speed centrifuge.
To provide the scientific community with the most clinically relevant study tool and to better understand lip epithelial biology, we aim to establish 3D human lip models using primary keratinocytes. So far, such a system is not available which is due to the lack of human lip tissue and the complex anatomical structure of lip tissue.
We isolate primary lip keratinocytes from surplus lip tissue that has to be excised during routine surgical cleft lip repair. This tissue is otherwise discarded but provides us with the ideal source for lip keratinocyte extractions. The human lip is a complex anatomical structure and represents a mucocutaneous junction where labial skin transitions into the oral mucosa (Figure 1). Consequently, an optimal lip model should be compromised of labial skin and oral mucosal keratinocytes that meet in a transition zone. For this purpose, immunohistochemical analyses are of utmost importance as they allow the distinction of keratinizing skin lip keratinocytes from non-keratinizing mucosal keratinocytes.
Fig1: Hematoxylin and Eosin staining of a representative lip tissue biopsy. The oral mucosa (left side) transitions into the labial skin (right side). Taken from Parisi L. et al., 2025.
With the funding provided by the Berne University Research Foundation, we purchased a reliable and temperature-monitoring laboratory-grade microwave oven (Figure 2A) as well as a universal oven (Figure 2B). This equipment is used to establish our own in-house immunohistochemical setup, which enables us to reproducibly stain limited amounts of lip tissues and 3D culture models. It enables us to maintain a standardized immunohistochemistry protocol of both high quality and safety standards, which should guarantee the integrity of the whole project. While the temperature-controlled microwave oven is routinely used in the laboratory to perform heat-induced antigen retrieval, the oven allows us to conduct key steps involved in the paraffin embedding process. Together, these instruments facilitate the whole staining process and represent an important improvement of both safety and quality in our laboratory.
Fig2: (A) Temperature-controlled microwave oven for heat-induced antigen retrieval protocols.
Fig2: (B) Universal oven for key steps in paraffin embedding.
We sincerely thank the Berne University Research Foundation for its valuable support of this work.
PD Dr. Martin Degen
Laboratory for Oral Molecular Biology Department of Orthodontics and Dentofacial Orthopedics zmk bern