Lars Norlén

Lars Norlén and his colleagues have identified the basic molecular structure of human skin. The findings pave the way for development of new drug formulations that can be delivered through the skin, reducing the risk of side effects.

Our skin protects us from water, chemicals, microorganisms, sun radiation and dehydration. Until recently, the understanding of how this protection is accomplished has been incomplete. Now, Lars Norlen and his colleagues have identified the basic molecular structure of the skin layer that forms this protecting barrier.

Arrangement of lipid molecules in the stratum corneum. The long chains of green balls represent hydrocarbon chains in ceramides, cholesterol and free fatty acids.

Their findings show that the barrier lies in the fat molecules, lipids, that occupy the space between the cells in the outermost layer of skin, the stratum corneum. Normally, lipids arrange themselves into a two-layered sheet, or bilayer, with all of their hydrophobic (water-repelling) tails pointing inwards and their hydrophilic (water-attracting) heads outwards. However, the lipid molecules in the stratum corneum are stretched-out, so that the two tails of each molecule point in opposite directions. The molecules are stacked on top of each other in an alternating fashion, forming a structure which is much more impermeable than a normal bilayer. The fat structure also allows for the horny layer cells to slide on each other, making the skin flexible and thereby contribute to its mechanical robustness.

Schematic drawing of skin. Left part: schematic cellular-scale drawing of epidermis. Mid part: molecular-scale drawing of the lamellar lipid structure occupying the space between the cells of the stratum corneum. Right part: atomic model of the lipid structure's repeating unit, composed of two mirrored subunits, each composed of one fully extended ceramide- (CER), one cholesterol- (CHOL) and one free fatty acid (FFA) molecule.

The researchers developed a novel experimental approach for this particular project, combining cryo-electron microscopy defocus series with molecular modelling and electron microscopy simulation. They freezed healthy, living, human skin to below -140 °C, preserving every molecule in its native location. They then sliced the tissue into layers 25 to 50 nanometres thick and examined the layers using an electron microscope.

The research has above all been driven by the vision of enabling drug administration through the skin instead of taking pills via the mouth, in order to increase efficacy and reduce side effects. The team now aim at developing a computer model of the skin, as well as artificial skin, for screening drugs and other chemicals that could potentially open the skin barrier.

Group members

  • Lianne den Hollander, MSc
  • Aurelie Laloeuf, MSc
  • Sergej Masich, Dr

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Selected publications

Iwai, I. Han, H. den Hollander, L. Svensson, S. Öfverstedt, L-G. Anwar, J. Brewer, J. Bloksgaard Mřlgaard, M. Laloeuf, A. Nosek, D. Masich, S. Bagatolli, L. Skoglund, U. Norlén, L

The human skin barrier is organized as stacked bilayers of fully-extended ceramides with cholesterol molecules associated with the ceramide sphingoid moiety.

J. Invest.Dermatol. 2012 Apr 26 (Epub ahead of print)

Norlén, L. Öktem, O, Skoglund, U

Molecular cryo-electron tomography of vitreous tissue sections: current challenges.

J. Microscopy, 2009, 235:293-307

Norlén, L. Al-Amoudi, A

Stratum corneum keratin structure, function, and formation: the cubic rod-packing and membrane templating model.

J Invest Dermatol, 2004, 123(4):715-32

Norlén, L

Skin barrier formation: the membrane folding model.

J. Invest. Dermatol, 2001, 117(4):823-829

Norlén, L

Skin barrier structure and function: the single gel-phase model.

J. Invest. Dermatol, 2001, 117(4):830-836