Hyaluronic acid (HA) is a ubiquitous component of extracellular matrix. Aft
er tissue injury, HA appears in greater abundance during the inflammatory r
esponse and the phase of clearance of cell and matrix debris, before collag
en production and matrix degradation. The aim of this study was to examine
whether normal rat renal fibroblasts were capable of HA synthesis and to de
termine the effect of HA on in vitro collagen production in a series of nor
mal rat cortical fibroblast cultures. Fibroblast cultures from both renal c
ortex and medulla were established from adult Sprague-Dawley rats. HA synth
esis was measured by radioimmunoassay, and incorporation of H-3-proline int
o collagen was used to determine collagen synthesis. Fibroblasts were defin
ed on the basis of morphology and alpha smooth muscle actin immunohistochem
istry. HA synthesis was measured in both renal cortical and medullary fibro
blasts at passage 3 for both 24 and 48 h in 5 animals and expressed as a fr
action of protein content. HA was synthesized by both cortical and medullar
y fibroblasts; however, cortical fibroblasts produced less HA than medullar
y fibroblasts at both 24 h (p = 0.05) and 48 h (p = 0.02). In normal cortic
al fibroblasts, exogenous HA suppressed overall total (cell and media) coll
agen production after a 22-hour labelling period (p = 0.002 compared to con
trols). Decreased collagen production was also found individually in cell (
p = 0.02) and media fractions (p = 0.01). Both cortical and medullary fibro
blasts are capable of synthesizing HA in vitro. Furthermore, the findings i
n this study suggest that HA may be an important mediator in reducing renal
cortical fibroblast collagen production and may play an important role in
limiting renal interstitial scarring. Copyright (C) 2001 S. Karger AG, Base
l.