Introduction to the topic:
Lars Jørn Jensen’s group (Cerebrovascular Physiology) studies arteriolar function in health and disease. We investigate fundamental mechanisms in regulation of arteriolar tone involved in the control of blood pressure and organ perfusion (with emphasis on the brain). We specialize in myogenic tone, flow-mediated vasodilatation, and structural remodeling, which are key determinants of vascular function in vivo.
We strive to describe new molecular mechanisms, and to apply this research using animal models of hypertension, aging and obesity/diabetes. In collaboration with the LifePharm In Vivo Pharmacology Centre (UCPH), we assist in development of porcine models of obesity and diabetes through our expertise in microvascular function.
Project details:
Basic characterization of the proteome expressed in small resistance arteries of the pig brain.
We are interested in mapping the following family of proteins: Multi-drug resistance proteins (PGP; MRP; BCRP); Claudins; Occludin; ZO-1; ROCK1/2; Rho-GEFs; Ga12; CaV3.X channels (T-type); CaV2.1 channels (P/Q-type); TRPA1; TRPC6; TRPV4; SKCa/IKCa channels; Kir2.x channels; KATP channels; Insulin-R; IGF1-R; TGFBR1-2; MCR1-4 Receptors. We want to map the expression and localization of these targets using standard molecular biological tools coupled with Mass Spectrometry in order to use the pig brain as a translational model to study human cerebrovascular function and disease. The experiments will be focused on immunofluorescence microscopy using specific antibodies recognizing epitopes of the expressed proteins mentioned above, and will clarify the cellular localization and the relative expression levels compared to a positive control sample. As such an exhaustive characterization has not previously been performed in the pig brain the results are likely to be published eventually (although not necessarily right after the course).
Selected relevant publications:
- Hansted AK, Jensen LJ, Olesen J, and Jansen-Olesen I. Localization of TRPA1 channels and characterization of TRPA1 mediated responses in dural and pial arteries in vivo after intracarotid infusion of Na2 Cephalalgia (accepted) (2020) (IF 4.438).
- Ludvigsen TP, Olsen LH, Pedersen HD, Christoffersen BØ, and Jensen LJ (Corr.). Hyperglycemia-induced transcriptional regulation of ROCK1 and TGM2 expression is involved in small artery remodeling in obese diabetic Göttingen Minipigs. Clinical Science 133, 2499-2516 (2019) (IF 5.237).
- Hansted AK, Bhatt DK, Olesen J, Jensen LJ, and Jansen-Olesen I. Effect of TRPA1 activator allyl isothiocyanate (AITC) on rat dural and pial arteries. Rep. 71, 565-572 (2019) (IF 2.787).
Prerequisites
One year each of biology and chemistry at university level.
Additional application required
You must submit an additional application through the Online Registration portal.
All application materials must be submitted on the following dates by midnight in your time zone:
- November 1 for spring semester applicants
- May 1 for fall semester applicants
Recommended experience
Basic knowledge of physiology and molecular biology is recommended.
Faculty
Lars Jørn Jensen
FacultyPh.D. in Physiology at the August Krogh Institute, University of Copenhagen (UCPH). Experience in the pharmaceutical industry (Lundbeck; development of anti-depressants). University researcher and teacher of cardiovascular physiology at UCPH from 2002 to present (currently associate professor). International research experience from Massachusetts General Hospital/Harvard Medical School, Boston, MA (1997-98) and Kyushu University, Fukuoka, Japan (2004-2006).
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