Background
The extracellular matrix actively participates in inflammatory signaling, tissue remodeling, and repair of various tissues. A better understanding of how components of the extracellular matrix participate in acute lung injury (ALI) and repair may provide new therapeutic targets for clinical conditions such as acute respiratory distress syndrome. Hyaluronic acid (HA) is an unsulfated glycosaminoglycan (extracellular matrix polysaccharide with repeating disaccharide unit) that can be covalently modified with the heavy chains (HC) of serum protein inter-alpha-inhibitor (IαI) during inflammation [
1‐
5], in a reaction exclusively mediated by tumor necrosis factor α (TNFα)-stimulated gene-6 (TSG-6) protein (Additional file
1). Building on reports that TSG-6 mediated formation of HC-modified HA is critical to neutrophil sequestration in liver sinusoids [
6,
7] and an important protective mediator of survival in lipopolysaccharide (LPS) models of sepsis [
6,
8‐
10], we investigated the role of HC-HA in ALI induced by respiratory infections, modeled by LPS or bacteria.
HC-modified HA is prominently featured in the extracellular matrix of chronic lung diseases such as pulmonary arterial hypertension [
11], asthma [
12], cystic fibrosis [
13], and idiopathic pulmonary fibrosis [
14], that share lung inflammation in their pathogenesis, suggesting that HC-HA formation is important in either promoting the onset or delaying the resolution of lung inflammation. We therefore used self-resolving models of ALI that were induced by intratracheal instillation of LPS or gram negative bacteria
Pseudomonas aeruginosa (PA) to study the kinetics and role of HC-modified HA in acute lung inflammation. In addition to using
TSG-6-knockout (KO) mice to address the functional role of HC-HA formation in ALI, we describe that LPS and
PA induce extensive HC-HA formation during the initial phase of injury, followed by fragmentation and clearance of HC-modified HA.
Materials and reagents
All materials and reagents used were from ThermoFisher (Waltham, MA, USA) unless otherwise specified. Reagents from Gibco (ThermoFisher) were used for cell culture.
Mice
All animal experiments in this paper were approved by the Institutional Animal Care and Use Committee (IACUC) at National Jewish Health.
TSG-6-KO mice (BALB/c background) were originally generated by Dr. Katalin Mikecz [
15]. Studies were conducted using sex- and age matched
TSG-6-KO mice and wild type (WT) and heterozygous (HT) littermate controls.
Murine acute lung injury models
Escherichia coli (E. coli) LPS (20 μg LPS in 50 μL phosphate buffered saline (PBS), L2880, MilliporeSigma, Burlington, MA, USA) or gram negative
PA bacteria (2 × 10
6 CFU, colony forming unit, PA01 strain) was instilled directly into the tracheas of 10–12 week old mice using a 22-gauge oral gavage needle (7920, Cadence Science, Cranston, RI, USA) with its distal 0.5 cm end bent 40° to facilitate tracheal insertion.
PA was provided by Dr. Kenneth Malcolm (National Jewish Health) and originally obtained from
Pseudomonas Genetic Stock Center (East Carolina University) [
15].
PA was grown in Luria-Bertani broth (LB), and
PA in the exponential phase of growth was centrifuged and resuspended in 50 μL PBS for instillation. CFU was confirmed by plating dilutions of
PA on LB agar. Mice weight was assessed every 24 h, for up to 6 days post-instillation.
Methods
Lung HC-HA
HC-HA formation in lung tissue was measured as described previously [
16] with minor modifications. Briefly, equal mass (50 mg) of flash frozen mouse lung tissue was homogenized in PBS for 3 min using Mini-Beadbeater-16 (Biospec, Bartlesville, OK, USA) and treated with 1 U of
Streptomyces hyaluronidase (389,561, MilliporeSigma) or PBS control for 45 min at 4 °C with mechanical agitation. Samples were then centrifuged (13,000
g, 5 min, 4 °C) and supernatants were then incubated (37 °C; 30 min) with mechanical agitation. The samples were then combined with Laemmli Buffer, separated by SDS-PAGE (Stain-free Criterion TGX 7.5% gels, Biorad, Hercucles, CA, USA) and transferred to Immobilon-P PVDF membrane (MilliporeSigma) using TransBlot Semi-Dry (Biorad). The western blot was probed using rabbit-anti-hIαI antibody (A0301, DAKO, Agilent, Santa Clara, CA, USA), which has been validated for detecting mouse IαI and HC-HA formation in injured mouse lung [
17]. ChemiDoc MP (Biorad) was used to image the Stain-free gels for total protein. Densitometry was performed using Image Studio Lite (Licor, Lincoln, NE, USA).
Messenger RNA (mRNA) studies
Total ribonucleic acid (RNA) was extracted from cultured cells using RNeasy Mini Plus (Qiagen, Germantown, MD, USA) and from whole lung using Trizol Plus RNA Purification Kit with on-column deoxyribonuclease (DNAse) digest performed using PureLink DNase. Mouse lung was homogenized in Trizol using Mini-Beadbeater-16 (Biospec); 1000–2000 ng of total extracted RNA was used to synthesize complementary DNA (cDNA) (High-Capacity cDNA Reverse Transcription). Real-time quantitative polymerase chain reaction (qPCR) was performed on the StepOnePlus System using Taqman Universal PCR Master Mix and Taqman probes:
hTSG-6 (Hs01113602_m1),
msTNFα (Mm00443258_m1),
msTSG-6 (Mm00493736_m1) [
18,
19],
msHAS1 (Mm03048195_m1),
msHAS2 (Mm00515089_m1),
msHAS3 (Mm00515092_m1),
msHYAL1 (Mm00476206_m1),
msHYAL2 (Mm01230688_g1),
msTMEM2 (Mm00459599_m1), and
msCEMIP (Mm00472921_m1). Relative mRNA expression was calculated using the double delta comparative (ΔΔCt) method and
18 s RNA endogenous control (Taqman Hs99999901_s1).
HA histology
Mice were euthanized by isoflurane overdose, bilateral thoracotomy, and perfusion of the lungs via the right ventricle using 10 mL of blood bank saline. LPS injured lungs were inflated with a PBS equilibrated solution containing 4% paraformaldehyde (PFA) (15,710, Electron Microscopy Sciences, Hatfield, PA, USA) and 0.33% low melting point agarose. Inflated lungs were immersion fixed overnight (24 h) in 4% PFA at 4 °C with gentle rocking and then sequentially incubated for 1 h in PBS and 4 h in PBS containing 25% sucrose and 25% optimal cutting temperature (OCT) compound. The lungs were then embedded in OCT compound and frozen using dry ice. Ten μm sections were cut using a cryostat and allowed to air dry before washing in PBS to remove OCT compound.
PA injured lungs were inflated with 10% neutral buffered formalin containing 0.25% low melting point agarose and then immersion fixed in 10% neutral buffered formalin overnight at room temperature before paraffin embedding and sectioning (3 μm). Paraffin embedded tissue sections were then mounted on slides and processed as follows: mounted tissues were deparafinized and rehydrated using successive incubations in xylene (3 × 5 min), 100% ethanol (2 × 5 min), 95% ethanol (2 × 5 min) and equilibration in PBS followed by water. The tissue was then placed in pressure cooker containing citric acid based antigen unmasking solution (Vector Labs, Burlingame, CA, USA) and microwaved.
Staining of lung sections was performed as follows: tissue sections were blocked using PBS solution containing 3% bovine serum albumin (BSA, MilliporeSigma) and 0.1% Triton X-100 (MilliporeSigma). Biotinylated hyaluronan binding protein (50 μg/100 μl stock, 385,911, MilliporeSigma), rabbit anti-human HC2 (NBP2–31750, Novus, Littleton, CO, USA), and rat anti-mouse CD68 (FA-11, Biolegend, San Diego, CA) were added at 1:100 and incubated overnight at 4 °C. Streptavidin Alexa Flour 488 (S-11223) was used at 1:1000. Cy3 donkey anti-rabbit (711–165-152, Jackson ImmunoResearch, West Grove, PA, USA) and Cy5 donkey anti-rat (712–175-153, Jackson ImmunoResearch) were used at 1:2000. Tissue was mounted using ProLong Gold AntiFade with DAPI and imaged using laser scanning confocal microscope 700 confocal (Zeiss, Jena, Germany).
Histologic ALI scoring
Unlavaged mice lungs were perfused as described above. The left lung was inflated at 20 cm H
2O with 0.25% agarose in 10% formalin and immersion fixed overnight in 10% formalin following current guidelines [
20]. The fixed lung was placed in a molding box, encased in agarose, and 3 mm thick transverse pieces (apex to base) of the lung were sliced to ensure adequate sampling of the entire lung for histological scoring. The lung pieces were paraffin embedded together, sliced at 3 μm thick, and deparafinized and rehydrated as described above. The slides were stained with Harris Hematoxylin (2 min), Clarifier 1 (1 min), Bluing reagent (1 min), Eosin Y (30 s), dehydrated, and mounted. 4–5 fields (400X total magnification) of each transversely sliced lung piece (4–5 pieces total) were scored by a pathologist using the scoring system published by American Thoracic Society [
20], which assigns weighted scores for five parameters of ALI injury and provides a final averaged score between 0 (no injury) and 1 (most severe).
Cell culture
Primary human alveolar macrophages (hAM) were obtained by bronchoalveolar lavage of de-identified non-diseased human explanted lungs and enriched by 2 h attachment to tissue culture treated plastic in Roswell Park Memorial Institute (RPMI) media with 1% penicillin/streptomycin. Non-adherent cells were removed by PBS wash. Indicated treatments were performed by incubating in RPMI media with 2% fetal bovine serum (FBS, HyClone, GE Healthcare, Marlborough, MA, USA) and 1X penicillin-streptomycin and either vehicle (0.1% bovine serum albumin in PBS), 20 ng/mL tumor necrosis factor α (TNFα, R&D, Minneapolis, MN, USA), or 50 ng/mL ultrapure E. coli LPS (LPS-EK, InvivoGen, San Diego, CA, USA) for either 6 h or 24 h.
Peripheral Blood Mononuclear Cell Derived Macrophages (PBDM) were enriched by negative selection from whole blood using DynaBeads Untouched Human Monocyte Kit and by attachment to tissue culture plastic. Treatment with macrophage colony stimulating factor (20 ng/mL MCSF, R&D) over six days was used to differentiate PBMC into macrophage-like cells. Macrophage differentiation was performed in RPMI under serum free conditions with supplemental 1X non-essential amino acids, 1 mM sodium pyruvate, 2 mM glutamine, and 1X penicillin-streptomycin for days 1–3 and with additional 10% FBS for days 4–6. For experiments, cells were incubated in RPMI media with 2% FBS and treated with indicated stimuli for 24 h.
BEAS-2B transformed human lung bronchial epithelial cells were cultured submerged in Dulbecco’s Modified Eagle Medium (DMEM), high glucose (4500 mg/L) media with 10% FBS and 1% penicillin/streptomycin. For experiments, cells were washed once with PBS and then incubated in basal DMEM media with 2% FBS and indicated stimuli for 24 h.
Wi38 primary human fetal lung fibroblasts were cultured using Minimum Essential Media (MEM) media with 10% FBS and 1% penicillin/streptomycin. Cells were used between passages 8–12 for experiments, during which they were incubated with the indicated stimuli in basal MEM media with 2% FBS.
Human adipose stromal/progenitor cells (ASC) isolation, expansion, and characterization have been previously described [
21‐
23]. Briefly, ASC were obtained by liposuction from three human donors (two abdominal and one flank lipoaspirate) and then digested using collagenase I (Worthington, Lakewood, NJ, USA) under mechanical agitation for 2 h at 37 °C and centrifuged at 300
g for 8 min to obtain a pellet containing the stromal vascular fraction. This fraction was filtered using 250 μm Nitex filters (Sefar America, Buffalo, NY, USA), and red blood cells were lysed using ammonium chloride potassium lysis buffer (154 mM NH
4Cl, 10 mM KHCO
3, and 0.1 mM ethylenediaminetetraacetic acid (EDTA)). Cells were then cultured using Endothelial Cell Growth Medium (EGM2-MV) media (Lonza, Allendale, NJ). Cells were used for experiments between passages 4–6. To stimulate TSG-6 secretion [
22], ASC were washed with PBS to remove residual FBS and then incubated in basal Endothelial Basal Medium-2 (EBM2) media (Lonza) with 20 ng/mL TNFα (R&D) for 24 h. Demographic information of the ASC donors have been described previously [
24].
Human TSG-6 (hTSG-6) western blot
Conditioned media was centrifuged to remove detached cells (5 min, 600 g) and then mixed with Laemmli buffer. Proteins were separated by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) using Stain-Free Criterion TGX 4–20% gradient gels (Biorad), transferred, and imaged similarly as HC-HA blots. The blot was probed using goat-anti-hTSG-6 antibody (AF2104, R&D).
hTSG-6 ELISA
Conditioned media was collected and centrifuged (600
g, 5 min) and human TSG-6 (hTSG-6) was measured as previously described [
22] using a highly sensitive sandwich ELISA developed using commercially available antibodies [
25] and validated by
TSG-6 small interfering RNA (siRNA) in human MSC [
25] and ASC [
22]. Briefly, Nunc MaxiSorp 96-well plates were coated with rat anti-hTSG-6 antibody (A38.1.20; Santa Cruz) diluted in 0.2 M sodium bicarbonate buffer. Detection was performed using biotinylated goat anti-hTSG-6 antibody (BAF2104, R&D), Streptavidin-HRP (R&D), HRP Substrate (R&D) and quenched using 1 M H
2SO
4. To determine the extent of TSG-6 secretion relative to cell number, viable cell numbers were assessed by trypan blue exclusion and counted by hemocytometer. Recombinant human TSG-6 (2104-TS-050, R&D) in the absence and presence of FBS (2%) was used for standard curve (Additional file
2), since we found that the presence of FBS lowered the magnitude of HRP substrate color development. This phenomenon may be due to TSG-6 forming TSG-6-HC covalent intermediate in the presence of IαI present in the serum and may explain why efforts to directly measure TSG-6 in human serum have been particularly challenging [
26].
Time-course of macrophage expression of TSG-6 and genes implicated in HA breakdown in LPS-challenged mice
Expression of mouse
TSG-6 (
msTSG-6), also known as
TNFα-induced-protein 6 (TNFAIP6), as well as
msHYAL1–2,
msTMEM2, and
msCEMIP was identified using Ensembl gene annotation data in a previously published data set. The detailed methods, pathway analysis of the RNA-sequencing (RNA-seq) data, and
National Center for Biotechnology Information (NCBI) deposition have been described here [
27]. Briefly, RNA-seq analysis was performed on bone-marrow-derived, recruited and resident macrophages isolated from bronchoalveolar lavage of intratracheal LPS treated mice (C57BL/6, 10–12 week old; 0, 3, 6, 9, and 12 dpi).
HA fragmentation assessment in whole lung
HA fragmentation in lung tissue was assessed using a protocol generously provided by Cleveland Clinic Program of Excellence in Glycoscience. Briefly, dedicated (non-lavaged) lungs were perfused with 10 mL blood buffered saline and flash frozen. Proteinase K (1 mg/mL) resuspended in 100 mM ammonium acetate (pH 7.0) with 0.01% sodium dodecyl sulfate was used to lyse 50 mg of tissue (24 h; 60 °C). 100% ethanol was added to precipitate glycoaminiglycans and samples were washed using 75% ethanol. Samples were resuspended in 100 mM ammonium acetate, and 100 °C heat was used to inactivate Proteinase K. Overnight benzonase treatment (MilliporeSigma) was used to degrade nucleic acids, and 100 °C heat was used to inactivate benzonase. 100 and 75% ethanol was then used to precipitate and wash the samples before resuspending in 100 mM ammonium acetate. Samples were equally divided and paired, having a half of the sample left untreated, and half treated with 0.2 turbidity reducing units (TRU) of
Streptomyces hyaluronidase (Seikagaku, amsbio, Cambridge, MA). All samples were lyophilized and resuspended in formamide (MilliporeSigma) for loading on 1% agarose gel (SeaKem HGT Agarose, Lonza). Gels were stained overnight in Stains-All (1.25 mg/200 mL in 30% ethanol), equilibrated in water, destained using light, and imaged using Cy5 695/55 epi-fluorescence filter on ChemiDoc MP [
28]. Select-HA of predetermined sizes (2500, 1000, 500, and 250 kDa HA) and Select-HA HiLadder (Hyalose, Oklahoma City, Oklahoma, USA) were used to size HA fragments. Densitometry of the distribution of HA staining was performed using ImageJ as described before [
29]. It has been described previously that agarose gel electrophoresis method is optimally suited for resolving high and medium molecular weight HA (> 200 kDa) and that chromatography and polyacrylamide gel electrophoresis can provide better resolution and quantification of low molecular weight HA [
30,
31].
HA staining characterization
Confocal Z-stacks were de-identified for the experimental group, and HA staining was blindly scored. Briefly, three to five representative 320 × 320 μm images of the left lung were taken from each mouse. From each image, HA staining in the peri-broncho-vascular interstitium was sampled by taking five 9.4 × 9.4 μm representative subselection snapshots. A max intensity Z projection was then prepared using the Fiji distribution of ImageJ [
32] and roughness was calculated by determining the surface area [
33] of the plotted intensity of HA staining using the SurfCharJ plugin [
34]. The roughness was normalized by dividing it by the average staining intensity of the snapshot. A mean normalized roughness was then determined for each mouse.
Bronchoalveolar lavage fluid (BALF) collection and flow cytometry
Tracheotomy was used to visualize the trachea and insert an 18-gauge angiocatheter (4075, JELCO-W, Smiths-Medical, Minneapolis, MN). BALF was obtained by five serial instillations (1 × 1 mL and 4 × 0.9 mL) of PBS containing 2 mM EDTA (a return of 4 mL of total BALF was consistently obtained with this protocol). For the total CD45+ count, aliquots of the five lavages were combined, blocked with CD16/CD32 (clone 93, eBioscience, ThermoFisher), stained with CD45 (30-F11, BD, Franklin Lakes, NJ, USA), and mixed with 123count eBeads (eBioscience). Cells used for total cell counts were stained and fixed without any centrifugation to avoid variability introduced by pelleting and aspirating. Using the absolute concentration of the counting beads added and the ratio of total CD45+ events to total bead events, the concentration of CD45+ cells was determined and then multiplied by 4 mL to obtain total CD45+ counts. For BALF cellular differentials, the five lavages were combined and centrifuged, blocked with CD16/CD32 (eBioscience), and stained with CD45 (30-F11, BD), Ly6G (1A8, Biolegend), CD64 (X54–5/7.1, BD), CD11c (N418, eBioscience), F4/80 (BM8, eBioscience), CD11b (M1/70, eBioscience), Siglec-F (E50–2440, BD), CD4 (RM4–5, Biolegend), and CD8a (53–6.7, Biolegend). Flow wash buffer consisting of PBS with 9% FBS and 0.5 mM EDTA was used to resuspend and wash cells. Flow data, which included minimum of 20,000 (PBS group) and 100,000 (LPS group) CD45+ leukocyte events for each sample, was collected using LSR II cytometer (BD) and analyzed using Flowjo (Ashland, Oregon, USA).
ELISA
Albumin-, receptor for advanced glycation end products (RAGE)-, and HA ELISAs were performed on the combined supernatant obtained from pelleting the first three BALF aliquots (total 2.6 mL volume). Manufacturer’s protocols were followed, using mouse albumin ELISA quantitation set (Bethyl Labs, Montgomery, TX); RAGE Duoset ELISA (R&D); HA Duoset ELISA (R&D), using sample dilutions of 1:3000; 1:6; and 1:4 (ctl group) or 1:12 (LPS group), respectively. Capture antibody coating and HRP detection were performed as described for TSG-6 ELISA.
Statistics
Statistical significance was calculated using ANOVA and Tukey’s multiple comparison test in Prism (Graphpad, La Jolla, CA). Data points from individual mice or independent experiments were plotted unless otherwise specified. Results were considered significant at P < 0.05.
Discussion
This study indicates that lung infections induce rapid covalent modification of HA, which was dependent on the evolutionarily conserved ability of TSG-6 to form HC-modified HA. In this context, alveolar macrophages may be an important source of secreted TSG-6 in the lung. Concomitant with HC-HA formation, we noted robust HA fragmentation which was independent of TSG-6. Both HC-modified HA and airway HA levels subsided with the resolution of lung injury. However, the TSG-6-dependent formation of HC-HA in this model did not have a major impact on the extent of lung inflammation and injury in this model.
Unlike other glycosaminoglycans (e.g. heparan sulfate, dermatan sulfate, chondroitin sulfate, and keratan sulfate), HA’s dissacharide backbone exhibits the least diversity, because HA cannot be covalently modified by sulfation, deacetylation, epimerization, and membrane-bound core proteins. Instead, the evolutionarily conserved TSG-6 mediated modification of HA’s N-acetylglucosamine with serum IαI’s HC is the only known HA covalent modification [
5,
45]. Preclinical LPS-induced endotoxic shock models of sepsis showed that HC-modified HA was required for neutrophil sequestration in the liver [
6,
7] and was overall protective for animal survival [
8,
9], indicating that endogenous TSG-6 secretion is important for the control of bacteria-induced inflammation and injury.
TSG-6- and
IαI-KO mice not only had worse endotoxic shock outcomes [
8,
9], but they also had markedly increased lung neutrophil infiltration [
8,
46], suggesting a protective role for TSG-6-mediated formation of HC-HA in the lung in controlling local neutrophil recruitment and accumulation, and/or a major reduction in the pool of recruitable neutrophils to other organs due to liver sequestration and removal of circulating neutrophils [
10].
Our data indicate a modest impact of TSG-6 on neutrophil levels in the bronchoalveolar lavage following lung instillation of LPS, suggesting that the lung production of TSG-6 may not be a major determinant of acute inflammatory cell accumulation, at least in ALI induced by lung rather than systemic endotoxin exposure. It is possible that in this more localized injury model, the levels of systemically absorbed LPS were insufficient to cause major formation of HC-modified HA in the liver with subsequent entrapment of neutrophils. In addition, since the HA expression in liver sinusoidal vasculature is 500- and 600-fold higher than in the lung vasculature both at baseline and during endotoxemia [
7], much higher levels of TSG-6 than those locally produced in ALI may be required to significantly modulate inflammation, including neutrophil trafficking across lung tissue barriers. This notion is further supported by the remarkable anti-inflammatory effects following treatment with exogenous recombinant TSG-6 in several conditions, including models of ALI [
8,
47]. These protective effects of exogenous TSG-6 have been ascribed to its ability to bind to and inhibit neutrophilic chemokines [
48‐
50], and may also be linked to an effect on bone marrow myeloid progenitor cell function [
22] and stromal cell differentiation [
51‐
53].
Our report is the first to use knockout mice to investigate the specific role of TSG-6 and HC-modified HA during bacterial lung infection. We found that there are similar trends toward greater neutrophilic inflammation during TSG-6 deficiency in both LPS and gram negative bacterial infection models of localized lung injury (Figs.
6a-b and
7). Since these trends were observed at time points of inflammation that directly followed (4 dpi, LPS) or coincided with (2 dpi,
PA) peak HC-HA levels, our data suggest that TSG-6 formation of HC-modified HA has modest effect on the abundance of inflammatory cells in the lung during acute infections. Considering the magnitude of the differences in BAL neutrophils and albumin levels, our results suggest that TSG-6 has a mild, protective role during acute lung inflammation. Given the well-established role of neutrophils in antibacterial defense [
54‐
56], future studies are needed to carefully dissect whether induction of TSG-6 and HC-modified HA in the lung has a protective or deleterious role in eliminating the gram negative bacterial infection. Additionally, the role of TSG-6 during gram negative bacterial sepsis has not been investigated and remains unclear, since the published reports on the role of TSG-6 and its covalent modification of HA during sepsis have been performed using systemic administration of LPS.
Our investigations expand on previous studies that implicated PBMCs as sources of TSG-6 in response to TNFα or LPS [
35,
36], by showing that terminally differentiated hAM are more versatile producers of TSG-6 compared to bronchoepithelial cells or lung fibroblasts. Furthermore, our comparative studies using adipose stem/progenitor cell suggested that hAM may be quite potent secretors of TSG-6 during acute inflammation. Locally produced TSG-6 may be essential for HC-HA formation in various lung compartments during bacterial or other types of inflammation associated with high TNFα levels, a cytokine implicated in the pathogenesis of a variety of acute and chronic lung diseases in humans [
57‐
59]. The local levels of TSG-6 produced in the lungs were not major determinants of acute lung inflammation and injury following LPS instillation. The only significant impact of TSG-6 deficiency in our study was that of a persistent increase in total inflammatory cell counts in bronchoalveolar lavage, with a trend of affecting particularly neutrophils during the resolution of inflammation. The functional significance of this effect remains to be determined in chronic or irreversible models of lung injury. Given the lack of differences in acute lung injury indices in
TSG-6-KO mice, we did not explore the role of TSG-6 on monocyte and macrophage function. This area has received recent attention in endotoxic shock models of systemic sepsis, where TSG-6 has been implicated in lung macrophage polarization [
8,
60], attributed to its modulatory effects on HA interactions with its receptor CD44 on monocytes [
61‐
63], or to a marked inflammatory milieu in
TSG-6-KO mice that could also impact macrophage functionality and programming [
8].
To our knowledge, this report is the first to characterize the kinetics of HC-HA formation and HA fragmentation and remodeling during LPS and
PA-induced reversible lung injury in mice. We noted HC-HA covalent interactions followed by rapid clearance of HC-modified HA during lung inflammation, suggesting a high HA turnover during ALI, which resolves within 4 days after LPS intratracheal instillation. Ability to form HC-HA paralleled the increase in lung levels of
TSG-6 and the availability of serum IαI (the source for HC) in the lung interstitium, as measured by correlations with markers of endothelial permeability (Additional file
9). The fact that the highest HC-HA levels coincide with peak alveolar permeability (BAL albumin and RAGE levels, 1 dpi) supports the hypothesis that vascular leak of serum-derived HC substrate into tissue is a critical step in the formation of HC-HA in lung tissue, as we have described before [
14]. Since TSG-6 was not required for the control of lung injury and barrier function, it is possible HC-HA formation is not required for control of lung injury, but necessary for other processes that were not investigated, such as airway epithelial cell survival and homeostasis [
64,
65].
Whereas HC-modified HA was not critical for the outcomes of ALI measured, future investigations will have to establish the functional role of HA fragmentation and remodeling in lung injury and repair. Unlike the accumulation and persistence of HC-modified HA observed in histopathological lesions of various chronic lung diseases, HC-modified HA in our models of ALI did not accumulate and was accompanied by markedly increased fragmentation of high molecular weight HA and/or de novo production of medium molecular weight HA products. Our study design could not differentiate between these two processes, nor did it carefully characterize the production of small molecular weight HA. The latter, however, were included in the total HA levels we measured in the bronchoalveolar lavage. These results suggest a key role of hyaluronidases in clearing HA to ensure resolution of acute lung inflammation, since hyaluronidase deficiency is associated with failure to clear HA and development of lung fibrosis [
66]. However, the transcription of both
HYAL1 and
HYAL2, which encode the principal hyaluronidases in human and mice [
67] were decreased in ALI lungs. Although the actual hyaluronidase activity may diverge from the abundance of its mRNA [
68], our data indicate that reactive oxygen species or other hyaluronidases may cause the marked HA fragmentation noted during ALI. We focused on two proteins that impact HA turnover whose genes are abundantly expressed in the lung: TMEM2 and KIAA1199/CEMIP [
39‐
41]. Of these, the expression of
CEMIP, a HA-binding protein that promotes HA degradation via clathrin-mediated endocytosis [
39] in the whole lung paralleled the kinetics of HA fragmentation in ALI. In turn, in alveolar macrophages, it was the expression of CD44 that increased during the resolution phase of ALI, which may indicate a role in the proper clearance of HA fragments. Future studies should investigate the relative contribution of enzymatic vs. non-enzymatic (i.e. reactive oxygen species) regulation of HA turnover in ALI.