MAP4K4 induces early blood-brain barrier damage in a murine subarachnoid hemorrhage model.

Sterile-20-like mitogen-activated protein kinase kinase kinase kinase 4 (MAP4K4) is expressed in endothelial cells and activates inflammatory vascular damage. Endothelial cells are important components of the blood-brain barrier. To investigate whether MAP4K4 plays a role in the pathophysiology of subarachnoid hemorrhage, we evaluated the time-course expression of MAP4K4 after subarachnoid hemorrhage. A subarachnoid hemorrhage model was established using the intravascular perforation method. The model mice were assigned to four groups: MAP4K4 recombinant protein, scramble small interfering RNA, and MAP4K4 small interfering RNA were delivered by intracerebroventricular injection, while PF-06260933, a small-molecule inhibitor of MAP4K4, was administrated orally. Neurological score assessments, brain water assessments, Evans blue extravasation, immunofluorescence, western blot assay, and gelatin zymography were performed to analyze neurological outcomes and mechanisms of vascular damage. MAP4K4 expression was elevated in the cortex at 24 hours after subarachnoid hemorrhage, and colocalized with endothelial markers. MAP4K4 recombinant protein aggravated neurological impairment, brain edema, and blood-brain barrier damage; upregulated the expression of phosphorylated nuclear factor kappa B (p-p65) and matrix metalloproteinase 9 (MMP9); and degraded tight junction proteins (ZO-1 and claudin 5). Injection with MAP4K4 small interfering RNA reversed these effects. Furthermore, administration of the MAP4K4 inhibitor PF-06260933 reduced blood-brain barrier damage in mice, promoted the recovery of neurological function, and reduced p-p65 and MMP9 protein expression. Taken together, the results further illustrate that MAP4K4 causes early blood-brain barrier damage after subarachnoid hemorrhage. The mechanism can be confirmed by inhibiting the MAP4K4/NF-κB/MMP9 pathway. All experimental procedures and protocols were approved by the Experimental Animal Ethics Committee of General Hospital of Northern Theater Command (No. 2018002) on January 15, 2018.

Chinese Library Classification No. R459.9; R363; R364

Introduction

Early brain injury (within 72 hours) was recently revealed to be a main contributor to the poor prognosis of subarachnoid hemorrhage (SAH) patients (Chen et al., 2014b). The pathophysiology of early brain injury after SAH involves injury of the neural vascular network, which contains the arterioles, capillaries, venules, astrocytes, neurons, microglia, surrounding support cells, and extracellular matrix (Zhang et al., 2012). The blood-brain barrier (BBB), which is a unit of the neural vascular network, plays a pivotal role in controlling the exchange of substances between the blood and the brain. Accumulating evidence suggests that targeting the BBB might provide benefits for SAH patients, but the precise mechanisms of BBB damage remain elusive (Xu et al., 2017; Sun et al., 2019).

Numerous findings have demonstrated that inflammatory reactions are the major contributor to BBB damage (Li et al., 2016; Xu et al., 2017; Sun et al., 2019). Matrix metalloproteinase 9 (MMP9) belongs to the matrix metalloproteinase protein family, and is reportedly crucial in the degradation of tight junctions and collagens, which make up the structure of the BBB (Sehba et al., 2012). Endothelial cells, located in the inner surface of vessels, secrete MMP9 under inflammatory conditions (Yang et al., 2014). Some drugs, including sulforaphane, AE1-329, and LP17, have been reported to reduce BBB injury after SAH, but the exact mechanisms remain elusive (Jang and Cho, 2016; Xu et al., 2017; Sun et al., 2019).

The sterile-20-like mitogen-activated protein kinase kinase kinase kinase 4 (MAP4K4) is expressed in endothelial cells and contributes to both atherosclerosis (Roth Flach et al., 2015) and inflammation (Aouadi et al., 2009). Vascular inflammation is considered to be an important process in BBB damage (Chen et al., 2014b), but it remains unknown whether MAP4K4 plays a key role in BBB injury after SAH. We speculated that targeting MAP4K4 after SAH may attenuate early brain injury by decreasing MMP9-associated BBB disruption.

Materials and Methods

Animals

In this study, 402 adult male C57B6J mice weighing 22–30 g and aged 3 months were provided by the Experimental Animal Center of the General Hospital of Northern Theater Command (General Hospital of Shenyang Military Command, Shenyang, China; license No. SCXK (Jing) 2014-0004). Mice were housed in a reversed 12-hour light/dark cycle environment. All experimental procedures and protocols were approved by the Experimental Animal Ethics Committee of the General Hospital of Northern Theater Command (approval No. 2018002) on January 15, 2018. The experimental procedure followed the United States National Institutes of Health Guide for the Care and Use of Laboratory Animals (NIH Publication No. 85-23, revised 1996).

Experimental design

The present study contained four stepwise experiments.

Experiment I

Protein expression differences of MAP4K4 over time and the cellular location of MAP4K4 after SAH were evaluated. For western blot experiments, 42 mice were randomly assigned to seven groups: sham, SAH 3-hour, SAH 6-hour, SAH 12-hour, SAH 24-hour, SAH 48-hour, and SAH 72-hour groups (n = 6 per group; ). MAP4K4 expression was detected by western blot assay in the cortex isolated from the ipsilateral (left) hemisphere. Six additional mice were assigned to the sham or SAH 24-hour groups for immunohistochemical experiments (n = 3 per group). Immunostaining of MAP4K4 and lectin (an endotheliocyte marker) was performed at 24 hours after SAH to confirm the expression of MAP4K4 on endothelial cells in the cortex.

Experiment II

To evaluate the intrinsic function of MAP4K4 and screen for the effective dose of MAP4K4 recombinant protein, 159 adult C57B6J mice were randomly assigned to eight groups: sham (n = 25), SAH (n = 12), SAH + normal saline (NS) (2 μL, n = 19), SAH + MAP4K4 10 ng/μL (n = 12), SAH + MAP4K4 50 ng/μL (2 μL, n = 19), SAH + MAP4K4 200 ng/μL (2 μL, n = 12), SAH + scramble (Scr) siRNA (2 μL, n = 25), and SAH + MAP4K4 siRNA (n = 25) groups (). Neurological impairment was evaluated via the modified Garcia score at 24 and 72 hours, as well as by the beam balance test (n = 6). Furthermore, brain water content was evaluated at 24 and 72 hours (n = 6). Evans blue permeability assessment (n = 6) was performed at 24 hours post SAH to evaluate BBB injury.

Experiment III

To investigate possible pathways of BBB damage, 60 adult C57B6J mice were assigned to five groups (n = 12 per group): sham, SAH + NS, SAH + MAP4K4 50 ng/μL, SAH + Scr siRNA, and SAH + MAP4K4 siRNA groups. Western blot assays were performed to detect phosphate-nuclear factor kappa-B (NF-κB; p-p65), zonula occludens-1 (ZO-1) and claudin 5 expression (n = 6; ). Zymography was used to detect MMP9 levels in the ipsilateral hemisphere of each group (n = 6). Immunostaining was also performed at 24 hours after SAH induction to detect endothelial continuity in the cortex (n = 3).

Experiment IV

To investigate the effects of PF-06260933 (PF), a MAP4K4 inhibitor, and screen for the optimal dose, 135 adult C57B6J mice were used. Mice were assigned to the sham (n = 31), SAH (n = 12), SAH + vehicle (double-distilled water, n = 31), SAH + PF 1 mg/kg (n = 12), SAH + PF 10 mg/kg (n = 31), and SAH + PF 100 mg/kg (n = 12) groups. The 1, 10, or 100 mg/kg PF (Merck, Darmstadt, Germany) was intragastrically administered at 15 minutes after SAH. Neurological impairment was assessed by the modified Garcia score and beam balance test at 24 and 72 hours after SAH (n = 6; ). Brain water content (n = 6) and Evans blue extravasation (n = 6) were used to analyze BBB injury. Tight junction protein degradation was evaluated by immunohistochemistry (n = 3), while western blot assays (n = 6) were performed to detect p-p65, ZO-1, and claudin 5 expression. Gelatin zymography was used to investigate the protein level of MMP9 (n = 6).

SAH models

Endovascular puncture models were established as previously described (Pan et al., 2017). Mice were anesthetized by intraperitoneal injection of pentobarbital sodium (40 mg/kg), and placed in a supine position. The left common carotid artery was isolated and the bifurcation was exposed by blunt dissection. The left external carotid artery was exposed distally to the digastric muscle, and the left internal carotid artery was exposed distally to the origin of the pterygopalatine artery. The external carotid artery was sheared distally, being careful to leave the longest possible stump. A 5-0 nylon suture was inserted from the left external carotid artery stump into the internal carotid artery, then pushed 3 mm through the bifurcation of the left internal carotid artery until resistance was felt (model establishment success). Internal carotid artery patency was confirmed after the suture was withdrawn, and the stump of the external carotid artery was then ligated. In the sham group, the operation was identical, but the suture was not pushed through the bifurcation of the internal carotid artery.

Intracerebroventricular injection

Intracerebroventricular injections were conducted as previously described (Zhao et al., 2017). A 1-mm-diameter hole was drilled 1 mm lateral to the bregma on the skull, without perforating the dura (Paxinos et al., 2001). The needle of a 10-μL Hamilton syringe (Microliter 701; Hamilton Company, Reno, NV, USA) was stereotactically inserted vertically into the hole to a depth of 3.0 mm, under the horizontal plane of the bregma. The needle penetrated the dura and was inserted into the left lateral ventricle. A 2 μL volume of recombinant MAP4K4 protein (Abnova, Taiwan, China) solution was infused at a rate of 0.2 μL/min at 1 hour after SAH induction, while 2 μL of MAP4K4 siRNA (Santa Cruz Biotechnology, Santa Cruz, CA, USA; 500 pmol in a 2-μL mixture of 1:1 RNase-free water and lipofectamine) or Scr siRNA (Santa Cruz Biotechnology; 500 pmol in a 2-μL mixture of 1:1 RNase-free water and lipofectamine) was infused at an identical rate at 48 hours before SAH induction.

SAH grade

The severity of SAH mice was evaluated with an 18-point grading system, as previously described (Chen et al., 2015). The basal cistern was divided into six areas, and each area was scored from 0–3 depending on the amount of clot in the SAH. The total score (0–18 points) was a summation of the six areas. Mice were excluded when scores < 8.

Neurological outcome evaluation

Neurological deficits were assessed as previously described (Dong et al., 2016). The modified Garcia score (Chen et al., 2015) and beam balance test (Wu et al., 2010) were used at 24 or 72 hours after SAH. The Garcia score included (1) spontaneous activity, (2) symmetry in the movement of all four limbs, (3) symmetry of the forelimbs, (4) climbing, (5) response to touch on either side of the trunk, and (6) response to vibrissae touch. Each part was scored from 0–3, as follows: 0, complete deficit; 1, deficit with function; 2, mild deficit; and 3, normal. The means of the neurological scores were from two blinded observers.

The procedures of the beam balance test were as follows: a beam (length 90 cm, width 1 cm) was placed between two platforms. Mice were pre-adapted to run freely on the beam before the test. Next, mice were placed onto the middle of the beam and ran to either side of the platform. Mice were scored based on their running performance, as follows: 0, fell off the beam within 40 seconds without moving; 1, did not move but stayed on the beam for at least 40 seconds; 2, moved not more than half the distance to the platform in 40 seconds and stayed on the beam for at least 25 seconds; 3, moved more than half the distance to the platform in 40 seconds and stayed on the beam for at least 25 seconds; 4, moved onto either platform within 40 seconds or moved to the platform within 25 seconds but did not get onto the platform; and 5, moved onto either platform in 25 seconds. An average score was calculated from three trials.

Brain water content

The brain specimens were carefully removed from the skull and separated into the left and right cerebral hemispheres, cerebellum, and brain stem, and then weighed (wet weight) on an analytical balance as previously described (Pan et al., 2020). The brains were then dried at 55°C in a drying system (DHG-9240A, Jing Hong Laboratory Instrument, Shanghai, China) for 48 hours, and then weighed again (dry weight). The final brain water content was calculated according to the formula:

Measurement of Evans blue extravasation

Evans blue extravasation was measured as previously described (Pan et al., 2017). After anesthesia with pentobarbital sodium (40 mg/kg) via intraperitoneal injection at 24 hours post SAH, Evans blue dye (2%, 5 mL/kg; Sigma-Aldrich, St. Louis, MO, USA) was injected into the left femoral vein over 2 minutes and allowed to circulate for 60 minutes. Phosphate-buffered saline (PBS) was then perfused through the left ventricle until clear liquid flowed from the incision of the right auricle. The brain samples were removed, and the left cerebral hemispheres were rapidly isolated and weighed. After being homogenized in saline, the samples were centrifuged at 15,000 × g for 30 minutes. The resulting supernatant was collected and mixed with the same volume of trichloroacetic acid. The mixture was incubated for at least 10 hours at 4°C, and then centrifuged again at 15,000 × g for 30 minutes. Next, the supernatant was collected and Evans blue dye was detected spectrophotometrically using a microplate reader (Thermo Fisher Scientific, Shanghai, China) at 610 nm (ultraviolet wavelength).

Immunofluorescence staining

Immunofluorescence staining was performed as previously described (Hao et al., 2016). Mice were deeply anesthetized by intraperitoneal injection of pentobarbital (40 mg/kg), perfused with pre-cooled PBS to remove blood, and fixed with 4% paraformaldehyde at 24 hours post SAH. Brain samples were immersed in 4% paraformaldehyde for 24 hours and then soaked in 40% sucrose for 24 hours. Coronal brain sections (10 μm) at 1.5 mm posterior to bregma were microtomed using a cryostat (Leica, Eisfeld, Germany) and immersed in 0.3% Triton X-100 for 1 hour at room temperature. Slides were then blocked with 5% donkey serum for 1 hour at room temperature before being incubated with anti-claudin 5 (tight junction protein marker, rabbit polyclonal; Abcam, Cambridge, UK), anti-MAP4K4 (rabbit polyclonal; Proteintech Group, Rosemont, IL, USA), and lectin (endotheliocyte marker; Vector Laboratories, Burlingame, CA, USA) antibodies at 4°C overnight. Sections were then incubated with appropriate secondary antibodies (donkey and goat polyclonal, 1:200; Cat#: A-11008, A-31572; Thermo Fisher Scientific) for 4 hours at room temperature. The sections were washed with PBS, and 4′,6-diamidino-2-phenylindole (DAPI; Beyotime, Shanghai, China) was added and incubated for 10 minutes at room temperature. After washing with PBS, the basal cortex was imaged using a fluorescence microscope (Olympus, Melville, NY, USA).

Western blot assay

Western blot assays were performed as previously described (Feng et al., 2017). Briefly, cytoplasmic, nuclear, and membrane proteins (cytoplasmic protein for detecting MAP4K4, nuclear protein for detecting p-p65, and membrane protein for detecting claudin 5 and ZO-1) were extracted from the ipsilateral hemisphere before being separated stepwise using a Subcellular Protein Fractionation Kit for Tissues (Pierce Biotechnology, Rockford, IL, USA) according to the manufacturer’s guidelines. Equal amounts of total protein (30 μg) were loaded into each lane of 10% sodium dodecyl sulfate polyacrylamide gel electrophoresis gels. The proteins were separated by electrophoresis and then transferred onto a polyvinylidene fluoride membrane. The membrane was subsequently blocked with blocking buffer for 2 hours at room temperature, and then incubated overnight at 4°C with the following antibodies: anti-claudin 5, anti-ZO-1, anti-phosphate-p65 (1:500, Cat# ab15106, ab96587, ab86299; Abcam) and anti-MAP4K4 (Cat# 55247-1-AP, Proteintech Group). β-Actin and histone H3 were used as the internal loading controls (1:2000; Cat# sc-47778, Santa Cruz Biotechnology; 1:500, Cat# PA5-16183, Thermo Fisher Scientific). The membranes were then incubated with the corresponding secondary antibodies (goat, 1:200, Cat# G-21234, G-21040; Thermo Fisher Scientific) for 2 hours at room temperature. The blots were imaged using enhanced Chemilucent Plus (Merck). Data were analyzed by densitometry using Quantity One (Bio-Rad, Berkeley, CA, USA). The densities of all bands were expressed as ratios against the sham group.

Gelatin zymography

Gelatin zymography was performed as previously described (Pan et al., 2017). Protein was extracted from the ipsilateral hemisphere of the mouse brain and separated by electrophoresis on 8% tris-glycine gel containing 0.1% gelatin, in tris-glycine sodium dodecyl sulfate running buffer. After electrophoresis, MMP9 was renatured by incubating the gel in renaturing buffer (Thermo Fisher Scientific) for 30 minutes at room temperature. The gel was then incubated in developing buffer (Thermo Fisher Scientific) before divalent metal cations were added and incubated at 37°C overnight. The gel was then washed with PBS and immersed in SimplyBlue (Thermo Fisher Scientific) for 30 minutes, with gentle agitation, to develop the MMP9 bands. The gel was imaged with a scanner and quantified using ImageJ software v1.48 (National Institute of Mental Health, Bethesda, MD, USA).

Statistical analysis

All data are expressed as the mean ± SD, and were analyzed using SPSS 18.0 software (SPSS, Chicago, IL, USA). Differences between groups were tested using one-way analysis of variance and Tukey’s post-hoc test. P < 0.05 was considered statistically significant.

Results

Mortality (Experiments I–IV)

In Experiment I, (0/6) mice died in the sham group, (1/6) died in the SAH 3-hour group, (1/6) died in the SAH 6-hour group, (0/6) died in the SAH 12-hour group, and (1/6) died in the SAH 48-hour group, caused by severe hemorrhagic volume. At 24 hours post SAH, mortality among the groups was as follows: (3/18) in the SAH group, (5/52) in the SAH + vehicle group, (1/6) in the SAH + MAP4K4 10 ng/μL group, (3/27) in the SAH + MAP4K4 50 ng/μL group, (1/6) in the SAH + MAP4K4 200 ng/μL group, (2/33) in the SAH + Scr siRNA group, and (2/33) in the SAH + MAP4K4 siRNA group. At 72 hours post SAH, mortality among the groups was as follows: (7/18) in the SAH group, (5/12) in the SAH + vehicle group, (3/6) in the SAH + MAP4K4 10 ng/μL group, (2/6) in the SAH + MAP4K4 50 ng/μL group, (3/6) in the SAH + MAP4K4 200 ng/μL group, (2/6) in the SAH + Scr siRNA group, and (3/6) in the SAH + MAP4K4 siRNA group. In the analysis of the results, 402 mice were involved; the excluded and dead animals were replaced by new ones.

Time course of intrinsic MAP4K4 expression after SAH (Experiment I)

There was a significant increase in MAP4K4 in the ipsilateral hemisphere at 12, 24, 48, and 72 hours after SAH (Figure and ). Furthermore, immunohistochemical staining in the sham group revealed that MAP4K4 colocalized with lectin, an endothelial marker, in the ipsilateral cortex (). At 24 hours post SAH, MAP4K4 was markedly elevated in endothelial cells ().

Time course of intrinsic MAP4K4 expression after SAH (Experiment I).

(A) Representative western blot bands of MAP4K4 expression after SAH. (B) Quantitative analysis of MAP4K4 from the ipsilateral hemisphere; the relative density of each protein was normalized to the sham group. Data are expressed as the mean ± SD (n = 6; one-way analysis of variance and Tukey’s post hoc test). *P < 0.05, vs. sham group. (C) Representative immunohistochemistry of MAP4K4 (red) and lectin (green) in the sham and SAH group at 24 hours after SAH (n = 3). Scale bar: 20 μm. DAPI: 4′,6-Diamidino-2-phenylindole; MAP4K4: sterile-20-like mitogen-activated protein kinase kinase kinase kinase 4; SAH: subarachnoid hemorrhage.

Neurological function after recombinant MAP4K4 delivery and interference of MAP4K4 expression after SAH (Experiment II)

There were no significant differences in SAH grading scores among the groups at 24 and 72 hours (P < 0.05; ). MAP4K4 siRNA effectively inhibited MAP4K4 expression after SAH (P < 0.05; Figure and ). Mice in the SAH group showed significant neurological dysfunction in the modified Garcia test and beam balance test compared with the sham group at 24 hours (P < 0.05; Figure and ). In addition, mice in the SAH + MAP4K4 50 ng/μL and SAH + MAP4K4 200 ng/μL groups had more severe neurological deficits at 24 hours post SAH compared with the SAH + NS group (P < 0.05; Figure and ). Moreover, MAP4K4 siRNA treatment led to improvements in neurological function compared with the SAH + Scr siRNA group at 24 hours (P < 0.05; Figure and ).

Neurological functions, brain water content, and blood-brain barrier permeability after recombinant MAP4K4 delivery and MAP4K4 silencing post SAH (Experiment II).

(A) SAH grading scores. (B, C) Representative western blot bands of MAP4K4 siRNA knockdown efficiency at 24 hours post SAH. (D, E) Modified Garcia scores and beam balance test results at 24 and 72 hours. (F, G) Brain water content at 24 and 72 hours after SAH. (H) Evans blue leakage in the ipsilateral hemisphere 24 hours post SAH. Data are expressed as the mean ± SD (n = 6; one-way analysis of variance and Tukey’s post hoc test). *P < 0.05, vs. sham group; #P < 0.05, vs. SAH + NS group; †P < 0.05, vs. SAH + Scr siRNA group. MAP4K4: Sterile-20-like mitogen-activated protein kinase kinase kinase kinase 4; SAH: subarachnoid hemorrhage; Scr: scramble.

BBB leakage after recombinant MAP4K4 delivery and interference of MAP4K4 expression (Experiment II)

Brain edema is considered an independent factor of poor prognosis after SAH, and BBB injury is an essential pathophysiological process that promotes edema (Macdonald and Schweizer, 2017). Mice in the SAH and SAH + NS groups had marked brain edema in the ipsilateral cortex. Brain edema was significantly increased in the SAH + MAP4K4 50 ng/μL and SAH + MAP4K4 200 ng/μL groups compared with the SAH + NS group, while MAP4K4 siRNA pretreatment reversed this effect (P < 0.05; Figure and ). We therefore chose MAP4K4 50 ng/μL for subsequent experiments. Evans blue extravasation in the left hemisphere was increased in the SAH, SAH + NS, and SAH + Scr siRNA groups at 24 hours after SAH compared with the sham group (P < 0.05; ). Furthermore, MAP4K4 50 ng/μL and 200 ng/μL treatment aggravated Evans blue extravasation compared with the SAH + NS group, while MAP4K4 siRNA infusion significantly reduced Evans blue leakage at 24 hours post SAH (P < 0.05; ).

Tight junction proteins and MMP9 expression after recombinant MAP4K4 delivery and specific inhibition of MAP4K4 expression (Experiment III)

As transmembrane proteins on the BBB, claudins are anchored into protein complexes, such as ZO-1, to maintain BBB integrity. Immunofluorescent staining was performed in the ipsilateral cortex, and the normally continuous structures of endothelial cells (lectin) and claudin 5 were discontinuous at 24 hours post SAH. MAP4K4 recombinant protein treatment worsened these injuries; however, MAP4K4 siRNA infusion reversed these disruptions at 24 hours after SAH (). These phenomena were speculated to activate NF-κB (p65) and MMP9 signaling. Western blot assay results indicated that the nuclear protein levels of p-p65 in the SAH group were elevated at 24 hours (Figure and ) after SAH. In addition, MMP9 zymography revealed enhanced MMP9 expression at 24 hours post SAH (P < 0.05; Figure and ). MAP4K4 administration increased the levels of nuclear p-p65 and MMP9 (P < 0.05; Figure , and ), and this trend was reversed by MAP4K4 siRNA pretreatment (P < 0.05; Figure , and ). The levels of ZO-1 and claudin 5 were decreased after MAP4K4 recombinant protein infusion, but were increased by MAP4K4 siRNA pretreatment (P < 0.05; Figure , and ).

Continuous endothelial cell and tight junction protein disruption after recombinant MAP4K4 delivery and MAP4K4 silencing post SAH (Experiment III).

Endothelium and tight junction discontinuity was demonstrated by lectin and claudin 5 staining in the ipsilateral cortex after MAP4K4 recombinant protein infusion and MAP4K4 siRNA pretreatment, at 24 hours post SAH, under a fluorescence microscope. n = 3. Scale bar: 20 μm. Endothelium and tight junction discontinuity was greater in the SAH group than in the sham group. MAP4K4 increased endothelium and tight junction discontinuity while MAP4K4 siRNA reversed those trends. Arrows indicate discontinuity of endothelial cells and claudin 5. Red: claudin 5; green: lectin; blue: DAPI. DAPI: 4′,6-diamidino-2-phenylindole; MAP4K4: sterile-20-like mitogen-activated protein kinase kinase kinase kinase 4; SAH: subarachnoid hemorrhage; Scr: scramble.

Protein expression of nuclear p-p65, tight junction proteins, and MMP9 activity in the ipsilateral hemisphere after recombinant MAP4K4 delivery and MAP4K4 silencing post SAH (Experiment III).

(A–D) Protein levels of p-p65, ZO-1, and claudin 5. p-p65 expression levels were elevated at 24 hours, and this effect was enhanced by MAP4K4 infusion and reversed by pretreatment with MAP4K4 siRNA. ZO-1 and claudin 5 expression had the opposite trend. (E, F) Representative gelatin zymography of MMP9 expression revealed that proteinase activity rose at 24 hours after SAH, and was enhanced by MAP4K4 infusion and reversed by pretreatment with MAP4K4 siRNA. The quantified density was normalized to the sham group. Data are expressed as the mean ± SD (n = 6; one-way analysis of variance and Tukey’s post hoc test). *P < 0.05, vs. sham group; #P < 0.05, vs. SAH + NS group; †P < 0.05, vs. SAH + Scr siRNA group. MAP4K4: Sterile-20-like mitogen-activated protein kinase kinase kinase kinase 4; MMP9: matrix metalloproteinase 9; SAH: subarachnoid hemorrhage; Scr: scramble.

Pharmacological MAP4K4 inhibition and BBB damage post SAH (Experiment IV)

PF, a highly selective small-molecule inhibitor of MAP4K4 (Ammirati et al., 2015), was administered after SAH. SAH grade did not significantly differ among the groups (P < 0.05; ). Doses of 10 and 100 mg/kg PF markedly improved neurological function and reduced brain water content, while 1 mg/kg did not (P < 0.05; Figure ). There were no significant differences in neurological score and brain water content between the 10 and 100 mg/kg groups, so we chose 10 mg/kg for further experiments (P < 0.05; Figure ). Evans blue extravasation was reduced by 10 mg/kg PF (P < 0.05; ). Immunohistochemical staining, western blot assay, and zymography results revealed that p-p65 activation and MMP9 expression decreased after PF administration (P < 0.05; Figures and ). PF also prevented the decreased protein levels of ZO-1 and claudin 5 (P < 0.05; Figure , , and ).

Neurological function, brain water content, and blood-brain barrier leakage after PF delivery post SAH (Experiment IV).

(A, B) SAH grading scores. (B, C) Modified Garcia scores and beam balance test results. (D, E) Brain water content at 24 and 72 hours after SAH. (F) Evans blue leakage at 24 hours. Data are expressed as the mean ± SD (n = 6; one-way analysis of variance and Tukey’s post hoc test). *P < 0.05, vs. sham group; #P < 0.05, vs. SAH + vehicle group. MAP4K4: Sterile-20-like mitogen-activated protein kinase kinase kinase kinase 4; PF: PF-06260933; SAH: subarachnoid hemorrhage.

Continuous endothelial cell and tight junction protein disruption after PF delivery post SAH (Experiment IV).

Endothelium (lectin) discontinuity and tight junction (claudin 5) degradation in the ipsilateral cortex after SAH. Endothelium and tight junction discontinuity was greater in the SAH + vehicle group than in the sham group. Endothelium and tight junction discontinuity was preserved by PF administration. Scale bar: 20 μm. Arrows indicate discontinuity of endothelial cells and claudin 5. Red: claudin 5; green: lectin, blue: DAPI. DAPI: 4′,6-Diamidino-2-phenylindole; PF: PF-06260933; SAH: subarachnoid hemorrhage.

Protein expression of nuclear p-p65 and tight junction proteins and MMP9 activity in the ipsilateral hemisphere after PF delivery post SAH (Experiment IV).

(A–D) Levels of p-p65 decreased, while the expression of ZO-1 and claudin 5 was restored after PF administration. (E, F) Representative gelatin zymography of MMP9 expression revealed that PF attenuated MMP9 expression after SAH. Data are expressed as the mean ± SD (n = 6; one-way analysis of variance and Tukey’s post-hoc test).*P < 0.05, vs. sham group; #P < 0.05, vs. SAH + NS group. MMP9: Matrix metalloproteinase 9; PF: PF-06260933; SAH: subarachnoid hemorrhage.

Discussion

The present study demonstrated that MAP4K4 increased after SAH, remained increased at 24, 48, and 72 hours, and was elevated in endothelial cells. Exogenous MAP4K4 protein administration worsened neurological deficits and brain edema at concentrations of 50 ng/μL and 200 ng/μL, while MAP4K4 silencing effectively reversed these trends. Moreover, administration of MAP4K4 induced BBB disruption by interrupting continuous endothelial cells and tight junctions. An investigation of the mechanisms indicated that MAP4K4 enhanced p-p65 nuclear translocation and activated downstream MMP9, which is a main factor in tight junction protein degradation. Taken together, MAP4K4 may be a potential target for reducing BBB degradation after SAH.

MAP4K4, also known as hepatocyte progenitor kinase-like/germinal center kinase-like kinase and Nck-interacting kinase, belongs to the sterile 20 family of kinases. These are expressed broadly in the brain and are involved in many pathophysiological processes, including development (Xue et al., 2001), cell motility (Vitorino et al., 2015), and inflammation (Roth Flach et al., 2015; Tu et al., 2018). MAP4K4 was found to phosphorylate moesin, and then displaces talin from INTb1 to inactivate b1-integrin and cause membrane retraction (Vitorino et al., 2015). MP4K4 is reportedly critical for NF-κB activation and enhances atherosclerosis (Roth Flach et al., 2015). As an atypical MAPK, previous studies have demonstrated that MAP4K4 is upstream of c-Jun NH2-terminal kinase signaling (Su et al., 1997; Collins et al., 2006), while other studies have revealed that MAP4K4 may not be required for MAPK activation (Danai et al., 2013; Wang et al., 2013).

Previous reports have also suggested that endothelial MAP4K4 enhances the upregulation of leukocyte adhesion molecule, promotes monocyte infiltration, and increases chemokine expression (Pannekoek et al., 2013; Vitorino et al., 2015). Atherosclerosis is a chronic disease whose etiological factor is speculated to be vessel inflammation. In the present study, MAP4K4 expression was elevated early (at 12 hours) and induced rapid BBB disruption at 24 hours post SAH, with discontinuous endothelial cells and tight junctions observed. It is difficult to attribute these phenomena to alterations of chemokines and adhesion molecules only. The best explanation may be that MAP4K4 activated NF-κB and downstream MMP9, but further studies are needed before any conclusions can be reached. This is the first report of MAP4K4 involvement in rapid vascular inflammation. In terms of mortality, there were no differences among the groups at 24 or 72 hours. These results are similar to those of our previous publications (Chen et al., 2015; He et al., 2015; Pan et al., 2017; Zhu et al., 2018), and suggest that intracerebral regulation of MAP4K4 preserves neurological function but does not reduce mortality after SAH. This phenomenon may be influenced by complex complications of the circulation system, respiratory system, electrolyte balance, systemic inflammatory response, or severe amounts of clot at the SAH ictus (Chen et al., 2014a; Lantigua et al., 2015).

The BBB is a highly selective neurovascular unit that can prevent harmful substances from entering the brain while allowing nutrients to enter (Keaney and Campbell, 2015). After SAH or other acute neurological injuries, BBB permeability is elevated. This increased permeability leads to blood metabolites directly contacting neurons and surrounding cells, which can cause neuronal death and vasogenic brain edema. Increased BBB permeability at the acute stage of subarachnoid hemorrhage has been reported to correlate with poorer outcomes in clinical research (Ivanidze et al., 2018; Lublinsky et al., 2019), and is an important manifestation of early brain injury. Endothelial cells are a main component of the BBB; transcellular transport and tight junctions help maintain BBB structure and function (Zhao et al., 2015). Matrix metalloproteinases, and especially MMP9, are essential for the development of vasogenic edema and BBB damage after various brain injuries, including SAH, ischemic stroke, and traumatic brain injury (Feiler et al., 2011; Egashira et al., 2015; Michinaga et al., 2018; Zuo et al., 2019). In the current investigation, we demonstrated that brain edema worsened and Evans blue extravasation increased after SAH, and that MAP4K4 expression levels increased in endothelial cells. Moreover, knockdown of MAP4K4 ameliorated downstream NF-κB activation and MMP9 maturation, leading to BBB protection. PF, which is an inhibitor of MAP4K4, has been demonstrated to reduce MAP4K4-induced inflammation (Roth Flach et al., 2015). We also revealed that MAP4K4-induced inflammation was eliminated by PF, and that neurological outcome and BBB disruption were improved by PF treatment after SAH. Together, these results indicate that PF may be a candidate treatment for SAH; however, further clinical trials are needed.

This study had some limitations. Our data are only focused on MAP4K4 expression, while details of the NF-κB/MMP9 pathway were not studied. After SAH, NF-κB translocates to the nucleus, elevates MMP9 transcription, and induces the degradation of basement membrane and tight junction proteins; these effects have been well illustrated in previous studies. In addition, MAP4K4 may be located extracellularly and might affect surrounding cells as a ligand. Consistent with previous studies, we found that endothelial cells expressed high levels of MAP4K4; however, it remains unclear whether the MAP4K4/NF-κB pathway is activated in other cells after SAH. Furthermore, other as-yet-unknown mechanisms of MAP4K4 on MMP9 expression cannot be excluded. In future studies, more data are needed regarding the expression of MAP4K4 in other cell types and to elucidate the precise mechanisms of downstream NF-κB and MMP9.

In summary, MAP4K4 plays a vital role in early brain injury after SAH. Increasing MAP4K4 leads to rapid vascular inflammation and BBB disruption, caused by the NF-κB/MMP9 pathway. Genetic and pharmacological inhibition of MAP4K4 protects neurological function and BBB integrity. By targeting MAP4K4, new light may be shed on the management of SAH patients.

Additional file: .

Table 1

Intervention information of experiment I

Experiment I (n=48)	Sham	SAH
		3 h	6 h	12 h	24 h	48 h	72 h
Western blot	6	6	6	6	6	6	6
Immunofluorescence staining	3				3

SAH: Subarachnoid hemorrhage.

Table 2

Intervention information of experiment II

Experiment II (n=159)	Sham	SAH	SAH+vehicle	SAH+MAP4K4 10 ng/μL	SAH+MAP4K4 50 ng/μL	SAH+MAP4K4 200 ng/μL	SAH+Scramble (Scr) siRNA	SAH+MAP4K4 siRNA
24 h siRNA effiency	6						6	6
24 h behavior test+brain water content	6	6	6	6	6	6	6	6
72 h behavior test+brain water content	6	6	6	6	6	6	6	6
24 h Evans blue extravasation	6		6		6		6	6
24 h Immunofluorescence staining	3		3		3		3	3

MAP4K4: Mitogen-activated protein kinase kinase kinase kinase 4; SAH: subarachnoid hemorrhage.

Table 3

Intervention information of experiment III

Experiment III (n=60)	Sham	SAH+ vehicle	SAH+MAP4K4 50 ng/μL	SAH+Scramble (Scr) siRNA	SAH+MAP4K4 siRNA
24 h Western blot assay	6	6	6	6	6
24 h Zymography	6	6	6	6	6

MAP4K4: Mitogen-activated protein kinase kinase kinase kinase 4; SAH: subarachnoid hemorrhage.

Table 4

Intervention information of experiment IV

Experiment IV (n=135)	Sham	SAH	SAH+vehicle	SAH+PF 1 mg/kg	SAH+PF 10 mg/kg	SAH+PF 100 mg/kg
24 h behavior text+brain water content	6	6	6	6	6	6
72 h behavior test+brain water content	6	6	6	6	6	6
24 h Evans blue extravasation	6		6		6
24 h Immunofluorescence staining	3		3		3
24 h Western blot assay	6		6		6
24 h Zymography	6		6		6

MAP4K4: Mitogen-activated protein kinase kinase kinase kinase 4; PF: PF-06260933; SAH: subarachnoid hemorrhage.