Premium
Propranolol targets the contractility of infantile haemangioma‐derived pericytes
Author(s) -
Lee D.,
Boscolo E.,
Durham J.T.,
Mulliken J.B.,
Herman I.M.,
Bischoff J.
Publication year - 2014
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1111/bjd.13048
Subject(s) - propranolol , contractility , medicine , cardiology
Summary Background Propranolol, a β‐adrenergic receptor ( AR ) antagonist, is an effective treatment for endangering infantile haemangioma ( IH ). Dramatic fading of cutaneous colour is often seen a short time after initiating propranolol therapy, with accelerated regression of IH blood vessels discerned after weeks to months. Objectives To assess a possible role for haemangioma‐derived pericytes (HemPericytes) isolated from proliferating and involuting phase tumours in apparent propranolol‐induced vasoconstriction. Methods HemPericytes were assayed for contractility on a deformable silicone substrate: propranolol (10 μmol L −1 ) restored basal contractile levels in HemPericytes that were relaxed with the AR agonist epinephrine. Small interfering RNA knockdown of β 2 ‐ AR blunted this response. HemPericytes and haemangioma‐derived endothelial cells were co‐implanted subcutaneously in nude mice to form blood vessels; at day 7 after injection, mice were randomized into vehicle and propranolol‐treated groups. Results HemPericytes expressed high levels of β 2 ‐AR m RNA compared with positive control bladder smooth muscle cells. In addition, β 2 ‐AR m RNA levels were relatively high in IH specimens ( n = 15) compared with β 1 ‐AR, β 3 ‐AR and α 1b ‐AR. Normal human retinal and placental pericytes were not affected by epinephrine or propranolol in this assay. Propranolol (10 μmol L −1 ) inhibited the proliferation of HemPericytes in vitro , as well as normal pericytes, indicating a nonselective effect in this assay. Contrast‐enhanced microultrasonography of the implants after 7 days of treatment showed significantly decreased vascular volume in propranolol‐treated animals, but no reduction in vehicle‐treated animals. Conclusions These findings suggest that the mechanism of propranolol's effect on proliferating IH involves increased pericytic contractility.