Introduction
Although axons in the peripheral nervous system (PNS) have the capacity to regenerate and reach distal targets after a mechanical injury, functional recovery is usually not complete [
1]. Successful axonal regeneration and functional reinnervation depends on different factors such as severity and site of nerve injury, age of the subject, and the distance that axons have to grow until they reach distal targets, among others [
2,
3].
After a peripheral nerve injury, the distal portion of the nerve undergoes progressive degeneration in a process called Wallerian degeneration (WD) [
4]. While WD in the PNS is fast, taking 14–21 days to clear axonal and myelin debris, it is dramatically slow in the central nervous system (CNS) [
5]. This fact has suggested that slow or deficient myelin and debris clearance from the injury site could create an inhibitory environment for axonal regeneration. Accordingly, Wld
s mutant mouse with a delayed WD shows impairment of axonal regeneration [
6,
7]. Thus, endogenous or therapeutic compounds increasing the speed of WD might enhance axonal regeneration and target reinnervation. WD begins with axonal degeneration, followed by myelin ovoid breakdown and myelin clearance by Schwann cells and resident and infiltrating macrophages [
8,
9]. The recruitment of resident macrophages to the injury site starts within hours while the infiltration of macrophages from blood begins 2–3 days after injury and peaks between 7 and 14 days [
10,
11]. Finally, myelin clearance is complete from 8 to 14 days after nerve injury [
12]. Some authors have classified WD in a two-stage process: the first one, an inflammatory process when pro-inflammatory cytokines such as IL-1β and TNFα are produced mainly by resident macrophages and Schwann cells, and a second stage of WD which aims at resolution of inflammation with secretion of anti-inflammatory cytokines such as IL-10 by infiltrated macrophages and Schwann cells [
13‐
16]. New insights into macrophage activation related to macrophage polarization and their pro-inflammatory or anti-inflammatory responses have been reported [
17,
18], and recently macrophages have been classified as M1 or “classically” activated macrophages and M2 or “alternatively activated” macrophages, depending on the profile of cytokines required for their activation [
19,
20]. Taken together, these data suggest that macrophages involved in WD might be polarized to the M1 phenotype on the first stage and to the M2 phenotype for the resolution of inflammation. Different markers have been suggested to be representative of the different phenotypes, such as CD206 (mannose receptor) or arginase I for M2 and iNOS or IL-1β for M1 phenotype [
20,
21]. Despite this important breakthrough in activated macrophage classification, only few studies have been published describing the M1/M2 macrophage phenotype after a peripheral nerve injury [
22,
23]. Overall, the differences seen between macrophage phenotype in the PNS and CNS could contribute to explain the differences between the effective WD process in the PNS in comparison with the CNS where WD is very slow and inhibitory factors for nerve regeneration remain in the damaged tissue. Thus, modulation of inflammation and macrophage polarization to a M1-M2 phenotype may represent a strategy to promote regeneration in the PNS and the CNS. However, additional studies are needed to firmly establish this hypothesis.
Activating/inhibitory immune receptors like CD200R, TREM2, and SIGLECs have been shown to mediate important functions in checkpoints for the modulation of neuroinflammation [
24,
25]. The CD300 family of activating/inhibitory receptors is composed in humans by six members that are able to form complexes on the cell surface through the interaction among their extracellular immunoglobulin domain [
26‐
31]. Their combination in a complex differentially modulates the signaling outcome, suggesting a mechanism of how CD300 complexes could regulate the activation of myeloid cells upon interaction with their natural ligands [
32]. All the CD300 family members share an extracellular region comprising a single Ig-like domain and were thought to have a myeloid lineage-restricted pattern of expression. However, the expression of CD300f was recently observed in microglia, oligodendrocytes, and neurons in vitro [
33]. The importance of this family of receptors is highlighted by the fact that one of its members, CD300a, is the second gene with strongest evidence for positive selection between human and chimpanzee [
34]. Moreover, CD300a and CD300f are among the genes with the highest upregulation after a spinal cord traumatic injury [
33]. The CD300 family contains two inhibitory receptors, CD300a and CD300f, both displaying a long cytoplasmic tail with a variety of different tyrosine-based motifs, that are able to recruit phosphatases like SHP1 and SHP2 and therefore deliver inhibitory signals. The most interesting difference between these molecules, besides their different pattern of expression, is the existence of two binding motifs for the p85 subunit of PI3Kinase in the cytoplasmic tail of CD300f. In fact, it has been shown that CD300f delivers in vitro both inhibitory and activating signals, thus revealing a remarkable functional duality of this receptor [
28,
35‐
38]. However, in vivo CD300f has shown to be mainly an inhibitory receptor, as shown in CD300f knockout animals using the experimental autoimmune encephalomyelitis (EAE) model of multiple sclerosis [
39] and very recently in several models of allergy [
40] and systemic lupus erythematosus [
36]. This latter study shows that mouse CD300f (CLM-1) recognized outer membrane phosphatidylserine and regulated the clearance of apoptotic cells, being macrophages derived from CD300f knockout mice deficient for phagocytosis of apoptotic cells. Other recent reports suggest the existence of other main ligands for mouse CD300f, as phosphatidylcholine or ceramide [
40,
41], and for human CD300f (IREM1), as sphingomyelin [
42]. Despite the importance of CD300f in the regulation of inflammation and clearance of cell debris and apoptotic cells, no data is available regarding the expression of CD300f or its ligands in the normal and lesioned nerve and its role in regeneration.
In the present work, we characterize peripheral nerve expression of CD300f after a crush injury and the presence of its ligands. Moreover, by using soluble receptor fusion protein CD300f-IgG2a, we show that the blockade of the interaction between the immunoreceptor and its ligands impairs axonal regeneration and modulates macrophage M1/M2 phenotype.
Materials and methods
Animal surgery and treatment
Both male and female adult (8–12 weeks old) Thy1-yellow fluorescent protein mice, line H (Thy1-YFP-H; Jackson Laboratories, Bar Harbor, USA) [
43], were used in these studies. All experimental procedures were approved by the IPMon Animal Care Committee and conducted according to international FELASA guidelines, national law, and ethical guidelines (Uruguayan Animal Care Committee).
The surgical procedure was carried out following sterile precautions. Mice were anesthetized with ketamine-xylazine (90–10 mg/kg) and the right sciatic nerve at the mid thigh level was exposed. Treatments were performed by direct injections at 45 mm from the tip of the third digit in 2 μl of sterile PBS, using a fine glass micropipette connected to a Hamilton syringe. Immediately after the injection and at the same position, the nerve was crushed in two different directions 30 s each time with fine forceps. The crush site was labeled with lamp black powder. The wound was closed with 5–0 mononylon Ethilon sutures (Ethicon) and disinfected. The sciatic and tibial nerves and the plantar skin were harvested at 24 h, 3, 10, and 28 days post lesion (dpl).
All nerve injections were performed in 2 μl PBS and at 10 μg/ml concentration of the following products: rCD300f-IgG2a (rat extracellular domain of CD300f fused to mouse IgG2a protein) or purified mouse myeloma IgG2a (Invitrogen, Cat. N° 026200).
Histological and immunohistochemical procedures
At 10 and 28 days post lesion (dpl), mice were deeply anesthetized with pentobarbitone and intracardially perfused with saline followed by 4 % paraformaldehyde in 0.1 M phosphate buffer solution. The sciatic nerve, including its main tibial branch, was dissected to the ankle level and harvested. A sciatic nerve segment 3 mm distal to the injury site was postfixed in 4 % paraformaldehyde for 3 h, transferred to 30 % sucrose, and frozen for further immunohistochemistry procedures. The tibial nerve was sampled in two, one segment of approximately 14 mm was washed with PBS 0.01 M and whole mounted on slides in Mowiol mounting medium, whereas another segment of 2 mm at the ankle level was dissected out, postfixed in 2 % glutaraldehyde in 0.1 M phosphate buffer, and processed for embedding in Epon resin for semithin section preparations.
The sciatic nerve was cut longitudinally in the cryostat (8 μm thickness) and stored at −20 °C until used. Non-specific antibody binding was blocked with PBS 0.01 M + 1 % Triton + 10 % fetal bovine serum for 1 h at room temperature. Sections were then incubated overnight at room temperature with the following primary antibodies: rabbit anti-Iba-1 (1:3000; Wako 019-19741), rat anti-mouse CD206 (1:500; Serotec MCA2235), rabbit anti-iNOS (1:500; Calbiochem 482728), and rat anti-mouse F4/80 (1:150; Serotec MCA497). Macrophages were also demonstrated using biotinylated Licopersicon esculentum (tomato) lectin (6 μg/ml; L9389; Sigma-Aldrich). After washes with PBS-Triton 1 %, sections were incubated for detection with appropriate secondary antibodies (Invitrogen) and DAPI. Controls were made to rule out nonspecific staining by incubation without the primary antibody.
For the recognition of mouse CD300f ligand, immunohistochemical stainings using a soluble fusion protein containing the extracellular domain of rCD300f fused to the Fc region of the IgG2a mouse heavy chain or control mouse IgG2a were performed (both at 10 μg/ml). The studies were done in teased fibres and cryostat sections.
For immunohistochemistry of teased fibres, sciatic nerves were freshly dissected out and immediately immersed in 4 % paraformaldehyde in 0.1 M phosphate buffer for 3 h. After washing with PBS, the perineural sheath was removed and nerve bundles were separated using a pair of fine needles. Teased fibres were blocked with PBS 0.01 M + 1 % Triton + 10 % fetal bovine serum for 1 h at room temperature and then incubated with the following primary antibodies: rabbit anti-MBP (1:100; Sigma-Aldrich M3821), rat anti-S100 (1:200; Sigma-Aldrich HPA006462), and rCD300f-IgG2a (10 μg/ml), overnight at room temperature. After washes with PBS-Triton 1 %, sections were incubated for detection with appropriate secondary antibodies (Invitrogen) and DAPI.
For quantification of skin innervation, plantar pads of the hindpaw were removed at 28 dpl and processed as described [
44]. Briefly, after being postfixed in 4 % paraformaldehyde and cryopreserved, 70-μm cryostat sections were obtained. Non-specific antibody binding was blocked with PBS 0.01 M + 0.3 % Triton + 1 % normal goat serum for 1 h at room temperature. Sections were then incubated in primary rabbit antiserum against protein gene product 9.5 (PGP9.5, 1:1000; Ultraclone) for 48 h at 4 °C. After several washes, sections were incubated for detection with appropriate secondary antibodies for 24 h at 4 °C and mounted on gelatin-coated slides. Five sections from each sample were used to quantify the number and density of nerve fibres present in the epidermis of the paw pads.
Tissue sections were examined using an Olympus IX81 microscope and images of the longitudinal sections were acquired at 20× with an AxioCam MRm Zeiss camera attached to a computer for further counts and imaging processing by using ImageJ software. Confocal images of teased fibres were acquired using a Leica TCS SP5 II confocal microscope.
Semithin sections (1 μm) were obtained from the tibial nerve blocks. Images of whole tibial nerve cross section were acquired at 10× with an AxioCam MRm Zeiss camera attached to a computer, while sets of images chosen by systematic random sampling of squares representing at least 30 % of the nerve cross-sectional area were acquired at 100×. Measurements of the cross-sectional area of the whole nerve as well as counts of the number of myelinated fibres were carried out by using ImageJ software.
Flow cytometry
Cell surface expression of the CD300f (CLM-1) was tested by indirect immunofluorescence following standard techniques using a monoclonal anti-CLM-1 from hamster and the corresponding isotypic control [
37,
39]. Cells from uninjured and crushed sciatic nerve were analyzed by flow cytometry at 3, 10, and 28 dpl as described previously [
45] with some modifications. Briefly, animals were perfused with PBS to eliminate blood. Crushed sciatic nerves were harvested, cut in little pieces, and passed through a cell strainer of 70 μm and the cell suspension centrifuged. Samples were incubated with anti-mouse CD16/CD32 (1:100; Biolegend, Cat N°101319) for 15 min at 4 °C to block the nonspecific binding of immunoglobulins to the Fc receptors. Cells were incubated with CD45-PerCP (Biolegend), CD11b-PE-Cy7 (Biolegend), F4/80-APC (eBioscience), and monoclonal hamster anti-CLM-1 antibody (5 ug/mL) which was a generous gift from Genentech (San Francisco, CA) or an isotypic control (armenian IgG hamster from Serotec, Cat N° MCA2356), in PBS for 30 min at 4 °C. After washing in PBS, cells were incubated with an anti-armenian hamster IgG-FITC secondary antibody (Biolegend, Cat N°405502) in PBS for 30 min at 4 °C (dilution 1:100). Samples were analyzed with BD FACSCanto II Flow Cytometer and FlowJo Software (BD Biosciences).
Evaluation of axonal regeneration
Tibial nerves from crushed sciatic nerves at 10 dpl were whole mounted onto microscope slides and coverslipped in Mowiol mounting medium. The number of YFP-positive fibres was visualized using an Olympus IX81 microscope. Regenerating axons were counted at 1-mm increments along the length of the tibial nerve beginning at 8–9 mm from the crush injury site. All evaluations were conducted by a researcher blinded to the treatment groups as described [
46].
Functional evaluation
The walking track sciatic functional index (SFI) test was also carried out to assess recovery of locomotor function. The plantar surface of the mouse hindpaws was painted with black ink prior to crossing a runway. Footprints corresponding to the operated and intact paws were easily identified. The print length (PL) and the distance between the first and fifth toes (toe spread, TS) and between the second and fourth toes (intermediate toe spread, IT) were measured. The three parameters were combined in the SFI [
47] to quantify changes in walking patterns. The SFI varies between 0 (for uninjured) and −100 (for maximal impaired gait). The walking track test was carried out prior to surgery to obtain baseline scores and then on days 4, 7, 10, 14, 17, and 28 dpl to assess the recovery of locomotor function. A researcher blinded to the treatment groups conducted all evaluations.
Isolation of RNA and QPCR
Previous to nerve harvesting, animals were perfused with ice-cold PBS to eliminate blood. Due to very low RNA recovery from each nerve, the RNA was isolated and purified from pooled homogenized nerves (from 1 mm proximal to 6 mm distal to the crush,
n = 6 per group as described in [
48] in TRIzol (SIGMA, T9424), and the aqueous phase was further purified using the Nucleospin RNA II Kit with RNase Free DNase treatment (Macherey Nagel 740955.50). RNA samples were reverse transcribed using M-MLV reverse transcriptase (Invitrogen 28025–013) and random primers. Quantitative PCR (QPCR) was performed using the following TaqMan reagents from Invitrogen/Applied Biosystems: TaqMan Fast Advanced Master Mix (1205919), exon-spanning probes for CD300f/CLM1 (Mm00467508_m1), IL-1b (Mm01336189_m1), iNOS (Mm00440502_m1), MRC1 (Mm00485148_m1), and IL-10 (Mm00439614_m1). The relative expression ratio is calculated using the real-time PCR efficiencies and the crossing point deviation of an unknown sample versus a control according to Pfaffl [
49]. Eucariotic 18S RNA endogenous control (FAM-MGB 4333760) was included in the model to standardize each reaction run with respect to RNA integrity and sample loading. QPCR was performed using the Corbett Rotorgene 6000 apparatus and software. Cycling conditions were 50 °C for 2 min, 95 °C for 10 min, followed by 45 cycles at 95 °C for 15 s and 60 °C for 1 min. [
48].
Production of rCD300f-IgG2a
Chinese hamster ovary (CHO-K1) cells were stably transfected with pSecTag/mIgG2a constructs [
26] and positive cells were selected with 250 mg/mL of Zeocin (Invivogen, San Diego, CA, USA). The chimerical protein was purified from the supernatant using a protein A-sepharose column (GE Healthcare, Pittsburgh, PA, USA) as described before [
26].
Phagocytosis assay
Ten days after the crush injury and the different treatments, mice were anesthetized and approximately 8 mm of the lesioned nerve distal to the injury site was obtained, epineurium dissected and discarded, and incubated in PBS + collagenase (2 mg/ml) for 30 min at 37 °C. After homogenization, single-cell suspensions from each nerve in separate wells were plated for 2 h in DMEM supplemented with 10 % fetal bovine serum and penicillin 100 U/ml, streptomycin 100 μg/ml and in the presence of fluorescent beads (1:1000; Life Technologies, F-8762). After several washes, cells were fixed in 4 % PFA and the number of beads per cell were quantified under epifluorescence microscope observation by a treatment-blinded researcher.
Data processing and statistical analysis
All data are shown as mean ± standard error of the mean (SEM). Statistical analysis of behavioral data (SFI) was determined using two-way repeated measures ANOVA followed by Bonferroni post hoc analysis. One-way analysis of variance (ANOVA) followed by Tukey’s post hoc analysis was used for experimental data with more than two experimental groups. A value of p ≤ 0.05 was considered to be statistically significant.
Discussion
In the present work, we show that both CD300f and its ligands are present in the non-injured peripheral nerve, and that CD300f mRNA and protein are increased after a crush lesion. Interestingly, a single injection of the CD300f-IgG2a soluble fusion protein into the injured sciatic nerve delays both axonal regeneration at 10 dpl and functional recovery but has no effects at long-term regeneration. This delayed regeneration is associated to a modulation in the number and phenotype of M1/M2 macrophages in the lesioned nerve.
Recent reports have shown that phospholipids as phosphatidylcholine or phosphatidylserine are ligands for CLM-1, the mouse orthologue of CD300f [
35,
36,
41]. Phosphatidylserine/CLM-1 interaction contributes to apoptotic cell clearance and hence to dampen inflammation [
35,
36]. Ceramide has also been described as a putative ligand for this receptor, contributing to dampening inflammatory reactions of mast cells in several allergy models by the activation of CLM-1 negative signaling [
40]. The interaction of activating/inhibitory immunoreceptors with lipids appears to be a more general phenomenon [
41]. For instance, some gangliosides and 3-O-sulfo-β-d-galactosylceramide (C24:1) are potential ligands for CD300b/CLM-7 [
57]. In the central nervous system, staining of the brain and spinal cord with rat or human CD300f-IgG2a showed a distinctive punctuate pattern, mainly in oligodendrocytes of the white matter [
50]. Accordingly, we show here a similar punctuate staining pattern with CD300f-IgG2a in peripheral nerves. Interestingly, by using teased nerve fibres and Thy1-YFP-H mice, we evidence the specific subcellular localization of the CD300f ligands to what appears to be the outer cell membrane of the non-myelinating S100-positive domain of myelinating Schwann cells previously described [
58] and not to the MBP-positive myelin sheath or the axonal compartment. However, we cannot discard the possibility that the ligand may also be present in non-myelinating Schwann cells or some component of the extracellular matrix. Although electron microscope procedures are necessary to determine its precise location, our confocal images suggest the localization of the ligand in the outer non-myelin Schwann cell membrane [
58]. The normal presence of the ligands in Schwann cells and oligodendrocytes point to supplementary roles in addition to the phosphatidylserine “eat me” signal or the ceramide-induced signaling previously described. Other authors have shown that CD200, the ligand for the inhibitory immune receptor CD200R, is expressed in Schwann cells in the intact nerve [
59]. In the CNS, this receptor induces a tonic anti-inflammatory signal contributing to set the threshold and magnitude of proinflammatory signaling [
24,
60]. Whether the ligand of CD300f expressed on Schwann cells and oligodendrocytes also contributes to the maintenance of this tonic anti-inflammatory state is an open question. Chang and co-workers showed that CD200 is downregulated after crush injury in the site of lesion [
59]. They hypothesized that, after nerve injury, CD200 is downregulated in order to decrease immunosuppression and enhance influx of macrophages and the inflammatory response to eliminate myelin and axonal debris. The ligands for CD300f do not decrease at least at 10 dpl, suggesting different signaling mechanisms for these two receptors. Interestingly, despite intense invasion of macrophages into the nerve, a very similar staining pattern was observed for the CD300f ligands, suggesting that macrophages do not bear the ligand. In accordance, microglial cells in vitro did not stain with CD300f-IgG2a [
50].
Recent findings suggest that the anti-inflammatory physiological state of most tissues is not only a passive state resulting from absence of inflammatory stimuli but an active condition that requires participation of several molecules responsible for the suppression of potentially inflammatory stimuli. Under this paradigm, a physiological function for the ligands of inhibitory receptors like CD200R, CD300a, or CD300f could be to contribute to the so-called “On” and “Off” signals [
61]. “Off” signals are constitutively present in the brain parenchyma and are expressed mainly by healthy neurons, whereas “On” signals are expressed by endangered or impaired neurons [
62]. The integration of all the inhibitory and activating inputs shapes the phenotype and response of microglial cells or macrophages accordingly. In fact, several activating and inhibitory receptors similar to CD300f like CD200R, TREM2, or SIGLECs have been reported to be key regulators of microglial and macrophage activation [
24,
25]. Thus, these mechanisms, including CD300f and its ligands, could also be in place for the interaction of macrophages and Schwann cells in the normal and injured PNS to regulate the inflammatory status.
CD300f has been reported to deliver both activating and inhibiting signals [
28,
35‐
37]. However, only inhibitory signals have been found on monocytic cell lines. For instance, crosslinking CD300f in the human THP1 monocytic cell line inhibited proinflammatory cell activation induced by several TLR ligands through a SHP1- and SHP2-mediated mechanism [
63]. The role of CD300f in the proinflammatory activation of primary human monocytes/macrophages in vitro has not been reported. Using CD300f-deficient mice in the EAE mouse model, it was shown that CD300f acts as a negative regulator of myeloid cell activity by suppressing the production of inflammatory cytokines, nitric oxide, and demyelination [
39], confirming the negative anti-inflammatory signaling exerted by CD300f on monocyte/macrophages. After nerve injury, we show that CD300f mRNA was increased from 1 dpl, peaking at 3 dpl, and decreasing at 28 dpl. The expression of the protein was demonstrated by flow cytometry. We found protein expression in a subpopulation of macrophages in non-injured nerves and also after a crush injury, where the expression peaked at 3 dpl. Interestingly, we observed few F4/80 negative cells that showed CD300f expression, a staining that could represent neutrophils or mast cells. Accordingly, CD300f expression has also been shown in neutrophils [
26,
31] and mast cells [
40], both of which participate in nerve injury and regeneration. The time window of appearance of CD300f positive cells correlates with the influx rate of monocyte/macrophages and neutrophils into the lesioned nerve [
11,
64,
65]. To assess the possible role of CD300f and its ligands after a peripheral nerve injury, we took advantage of the description that CD300f receptor-ligand interaction could be blocked using CD300f-Fc fusion proteins, rendering identical results than those observed in CD300f knockout animals. For example, in the EAE model, CD300f-Fc worsened clinical scores to similar levels than CD300f KO mice [
39,
40]. Moreover, intradermal pretreatment with CD300f-Fc enhanced passive cutaneous anaphylaxis responses in wild type but not in CD300f KO mice [
40]. These results suggest that the effect of CD300f-Fc proteins is mediated by dampening CD300f signaling by an uncoupling of CD300f and its ligand rather than by directly activating signaling by the interaction of the soluble CD300f-Fc with the ligand. Interestingly, we show that dampening CD300f signaling using the soluble CD300f-IgG2a fusion protein-induced accumulation of macrophages that displayed an M2 alternative activation phenotype including increased CD206 and decreased iNOS expression. Whether this is a direct effect of dampening macrophage CD300f signaling or an indirect effect remains to be elucidated. Despite injection of the soluble receptor CD300f-IgG2a at the moment of the lesion, no acute changes on mRNA for CD206, iNOS, IL-1β, IL-10, or endogenous CD300f were observed at 1 dpl. This suggests a more complex and long lasting mechanism of Schwann cell and macrophage interactions determining the altered inflammatory response and delayed regeneration observed. In addition to the modulation of the proinflammatory phenotype, CD300f may also contribute to dampen inflammatory reactions promoting phagocytosis of apoptotic cells [
36]. Phagocytosis of myelin and cell debris is a critical component of WD and successful regeneration [
5]. The impaired regeneration after the single injection of CD300f-IgG2a might be related to inhibition of phagocytosis and thus delayed debris clearance. Accordingly, at 10 dpl, when no CD300f-IgG2a remains, the accumulation of debris may trigger the increased phagocytosis of nerve cells observed here that may be responsible for the delayed but successful regeneration at 28 dpl.
Despite the importance of macrophage phenotype in WD and axonal regeneration, only a few reports [
22,
23] have described the expression of M1/M2 phenotypic cell markers after nerve injury and repair. In a recent paper, Ydens and colleagues made a description of the different markers of M1 and M2 macrophages after nerve transection and repair in mice, showing a rapid M2 polarization of macrophages after axotomy [
22]. They evaluated a high number of markers of inflammation including iNOS, CD206, and IL-1β at different time points after nerve injury and mainly by QPCR. In accordance with our results, they observed a rapid fast induction of mRNA for IL-1β and IL-10 at 1 dpl. Moreover, they observed the upregulation of other M2 markers like Arg1, Ym1, or TREM2. They also reported that the mRNA for CD206 did not show changes at the different time points evaluated (until 14 dpl). In accordance, we did not observe notable changes in CD206 mRNA at 1 dpl or in protein level at 10 dpl in comparison with uninjured nerves. However, we also analyzed longer time points (28 dpl) to sample processes of resolution of the neuroinflammation and found an increase in CD206 staining in comparison with both uninjured and 10 dpl control injured sciatic nerves. This late increase might be a consequence of signals aimed to resolve inflammation by adjusting macrophage polarization towards a healing phenotype. In relation to M1 macrophage polarization after nerve injury, Ydens and colleagues did not show a significant change in iNOS, IL-12p40, or INFγ mRNA levels at the different time points post lesion studied. However, in the present work, we have seen a significant increase in the iNOS mRNA at 24 h after lesion and in the iNOS protein at 10 and 28 dpl. These differences in the results could be due to the type of nerve lesion used between the two studies, i.e., nerve section or nerve crush. Further experiments are needed to establish the effect of the different M1/M2 markers on nerve neuroinflammation and regeneration. In this line, we show that the manipulation of the CD300f/ligand interaction induces impairment of regeneration associated to important changes in M1/M2 markers. After a sciatic nerve crush injury, a single injection of CD300f-IgG2a significantly increased the number of tomato lectin-positive macrophages and CD206-positive cells and decreased iNOS immunoreactivity at 10 dpl, whereas an opposite effect was found at 28 dpl. These data suggest that blocking CD300f-ligand interactions not only contributes to an enhanced recruitment of macrophages but also to a change in the phenotype of normally recruited macrophages towards an early M2 phenotype, followed by a switch to a M1 phenotype of some macrophages later on. Interestingly, Mokarram and colleagues induced a nerve section followed by tubulization repair and IL-4 or INFγ treatment to polarize macrophages towards a M2 or M1 phenotype, respectively. Only IL-4 but not INFγ treatment induced increased Schwann cell migration, macrophage recruitment, macrophage polarization towards M2 phenotype, and regeneration [
23]. In the absence of any treatment, they reported a main macrophage polarization towards an M1 phenotype at 21 dpl, while we show mainly a polarization towards an M2 phenotype at 28 dpl. Moreover, Mokarram and colleagues reported that the increase in CD206-positive cells at 21 dpl positively correlated with regeneration, while we observe in fact a negative correlation at 10 dpl and no correlation at 28 dpl. This apparent contradiction between both studies may be explained by the different nerve injury models, i.e., nerve crush versus section and tubulization, where the neuroinflammatory conditions are different and where the structural maintenance of the epi-, peri-, and endoneurium has strong effects. Moreover, the treatment with IL-4 may change fundamental endogenous neuroinflammatory mechanisms influencing the final outcome of regeneration observed.
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
NL and HP conceived the study, designed and carried out most of the experiments, and wrote the manuscript. PS carried out the functional evaluation and part of the immunohistochemistry assays. MLN and JS produced and purified the CD300f-IgG2a fusion protein. NL, IFQ, and RLV performed the FACS analysis. XN, RLV, and JS contributed to the interpretation of the results and discussion. All the authors read and approved the final manuscript.