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September 09-10, 2019 | Edinburgh, Scotland

2

nd

Global Summit on

3

rd

International Conference on

Dermatology and Cosmetology

Wound Care, Tissue Repair and Regenerative Medicine

Joint Event

&

Journal of Dermatology Research and Skin Care | Volume 3

Dermatol Res Skin Care, Volume 3

Annexin A1 contained in extracellular vesicles promotes the activation of keratinocytes by

mesoglycan effects: An autocrine loop through syndecan-4 pathway and formyl peptide

receptors

Antonello Petrella

University of Salerno, Italy

W

ound healing is a dynamic process comprising

multiple

events,

such

as

inflammation,

re-epithelialization and tissue remodelling. Re-

epithelialization phase is characterized by the

engagement of several cell populations, mainly of

keratinocytes that sequentially go through cycles of

migration, proliferation and differentiation to restore

skin functions. Over the last decades, the efforts aimed

to find new pharmacological approaches for wound care

were made; yet almost all current therapeutic strategies

used remain inadequate or even ineffective. As such,

it is crucial to identify new drugs that can enable a

proper regeneration of the epithelium in wounded skin.

We have investigated the effects of the fibrinolytic drug

mesoglycan, a glycosaminoglycans mixture derived from

porcine intestinal mucosa, on HaCaT human keratinocytes

that were used as

in vitro

experimental model of skin

re-epithelialization. We found that mesoglycan induces

keratinocyte migration and early differentiation by

triggering the syndecan-4/PKCα pathway and that these

effects were, at least in part, because of the formation

of the annexin A1 (ANXA1)/S100A11 complex. Moreover,

syndecan-4 participates to the formation and secretion

of microvesicles (EVs), which may contribute to wound

healing. We found that the mesoglycan increases the

release of EVs which amplify its same effects. ANXA1

contained in the microvesicles is able to promote

keratinocytes motility and differentiation by acting on

Formyl Peptide Receptors (FPRs). Thus, the extracellular

form of ANXA1 may be considered as a link to intensify the

effects of mesoglycan.

Our work, for the first time, identified an interesting

autocrine loop ANXA1/EVs/FPRs in human keratinocytes,

induced by mesoglycan. Taken together, these data suggest

that mesoglycan may represent a useful pro-healing

drug for skin wound care. Its effects are triggered by the

syndecan-4 activation, which leads to the ANXA1 secretion

and the formation of a positive loop through FPRs.

Speaker Biography

Antonello Petrella is currently working as a professor of pharmacology

at University of Salerno-Department of Pharmacology, Italy. He has over

60 publications that have been cited over 1300 times, and his publication

H-index is 23 and has been serving as an editorial board member of

reputed Journals.

e:

apetrella@unisa.it