Cleavage of hyaluronan is impaired in aged dermal wounds

MJ Reed, M Damodarasamy, CK Chan, MNR Johnson… - Matrix Biology, 2013 - Elsevier
MJ Reed, M Damodarasamy, CK Chan, MNR Johnson, TN Wight, RB Vernon
Matrix Biology, 2013Elsevier
Changes in extracellular matrix (ECM) are one of many components that contribute to
impaired wound healing in aging. This study examined the effect of age on the
glycosaminoglycan hyaluronan (HA) in normal and wounded dermis from young (4–6month-
old) and aged (22–24month-old) mice. HA content and size were similar in the normal
dermis of young and aged mice. Dermal explants labeled with [3H]-glucosamine showed
decreased generation of smaller forms of HA in aged explants relative to young explants …
Changes in extracellular matrix (ECM) are one of many components that contribute to impaired wound healing in aging. This study examined the effect of age on the glycosaminoglycan hyaluronan (HA) in normal and wounded dermis from young (4–6month-old) and aged (22–24month-old) mice. HA content and size were similar in the normal dermis of young and aged mice. Dermal explants labeled with [3H]-glucosamine showed decreased generation of smaller forms of HA in aged explants relative to young explants. Aged mice exhibited delayed wound repair compared with young mice with the greatest differential at 5days. Expression of hyaluronan synthase (HAS) 2 and 3, and hyaluronidase (HYAL) 1–3 mRNA in wounds of young and aged mice was similar. There was a trend toward a decreased HYAL protein expression in aged wound dermis, which was accompanied by changes in detectable HYAL activity. Total HA content was similar in young and aged wound dermis. There was significantly less HA in the lower MW range (~250kDa and smaller) in 5-day wound dermis, but not in 9-day wound dermis, from aged mice relative to young mice. We propose that decreased cleavage of HA is an additional component of impaired dermal wound healing in aging.
Elsevier