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江苏新高考模式对高中生物实验教学影响的调查研究
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新出的EasyControl控制系统--——DIY的好伙伴
新出的EasyControl控制系统--——DIY的好伙伴
1.windows绿色软件免安装，以太网接口免驱动。
2.准确回零。限位开关配置方便。
3.手轮操作方便平滑。
4.对刀准确。
5.工件坐标系方便设置。
6.刀补功能。
7.可实现四轴。
8.完整的显示功能。
9.PWM输出控制主轴转速,可测主轴转速。
10.快捷键操作方便。
11.vc++6.0二次开发例程序。
基于PC的CNC控制系统。
主要由两部分组成：
1.Windows系统上的控制软件。绿色不用安装，可以直接运行。以太网接口，不用安装驱动。基于超过
10年的开源最成功的还在开发的全世界都在用的LINUXCNC（EMC2）()系统。代码完
全用原代码。只做部分接口修改。linuxcnc在linux上运行，是实时系统，安装复杂。但全球研究这个
系统的人很多。目前常见的MACH3、USBCNC等WINDOWS上的软件可以说都是基于LINUXCNC。
USBCNC的软件界面上直接就有链接。mach3开放的代码可看到用了大部分
LINUXCNC的代码。本系统从界面到内核完全忠于原著。编译器也是用GCC。用原代码，以不增一
分，不减一分为高境界。
2.控制板。控制板用三个主要芯片ARM的STM32F207,FPGA的EP4CE6E22C8N,以太网接口的DP83848构
成。四层板精心布板。对外光电全隔离。板上软件通过以太网接口可升级。以太网接口通信稳定。
09:39 上传
点击文件名下载附件
下载积分: 刨花 -2
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09:39 上传
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你的这东西到底是控制什么的，我知道的雕刻机，要么是打印机接口的MACH3，要么是USB接口的维宏
wxr1 发表于
我百度了一下，没找到EasyControl的内容，难道是你自己开发的?有官网吗？打印机接口的雕刻机能用吗？
您好，这个系统是我们开发的。
打印机接口现在的电脑不多了，就不支持了。
目前只支持我们的以太网接口的控制板。
欢迎关注！
我百度了一下，没找到EasyControl的内容，难道是你自己开发的?有官网吗？打印机接口的雕刻机能用吗？
wxr1 发表于
你的这东西到底是控制什么的，我知道的雕刻机，要么是打印机接口的MACH3，要么是USB接口的维宏
您好，这是控制板的图片。
(72.38 KB, 下载次数: 8)
11:40 上传
(65.75 KB, 下载次数: 1)
11:40 上传
和usb的比有何优势
cqswl 发表于
和usb的比有何优势
1.这个控制板输出可达1M,当前的板大部分是500K以下。
2.以太网的连接比USB的更稳定。
3.电脑上的软件与控制板是同一家做的，整体上会更稳定，配合更好。
4.本系统会比较适合已已有当前的控制系统可用，但还在找新的更好的系统的DIY的老手。
5.系统在回零的准确上，在手轮的好用流畅上是有明显的优势的。
6.原厂开发，有新要求可以迅速响应。
7.这是当前国产的可与mach3和usbcnc比肩的笔记本可用的第一个产品。
软件运行界面
(83.48 KB, 下载次数: 1)
13:21 上传
看了看，好像是推荐产品的吧
支持NURBS功能不？？？？？
mayb23 发表于
支持NURBS功能不？？？？？
14.7 G5.1 Quadratic B-spline
G5.1 X- Y- I- J-
• I - X axis offset
• J - Y axis offset
G5.1 creates a quadratic B-spline in the XY plane with the X and Y axis only. The offsets are I for X axis and J for Y axis.
It is an error if:
• I and J offset is not specified
• An axis other than X or Y is specified
• The active plane is not G17
14.8 G5.2 G5.3 NURBs Block
G5.2 X- Y- P- &L-&
X- Y- P- &L-&
Warning: G5.2, G5.3 is experimental and not fully tested.
G5.2 is for opening the data block defining a NURBs and G5.3 for closing the data block. In the lines between these two codes
the curve control points are defined with both their related weights (P) and their parameter (L) which determines the order of the
curve (k) and subsequently its degree (k-1).
Using this curve definition the knots of the NURBs curve are not defined by the user they are calculated by the inside algorithm,
in the same way as it happens in a great number of graphic applications, where the curve shape can be modified only acting on
either control points or weights.
数码家园 发表于
看了看，好像是推荐产品的吧
是有些推荐产品的。
不过不是完全的推荐产品。
1.楼主用的技术是开源的，不过入门是比较高的。可以让大家知道做一个控制系统不是想像中的那么高。
& &您去linuxcnc.org上下载代码，编译，研究，您也可以做出一个控制系统的。
2.可以发机械的做机器的，当然发控制器的做出的东东也是可以的吧。
EasyControl 发表于
是有些推荐产品的。
楼主，我支持你介绍新产品。请问价钱如何？
newnew007 发表于
楼主，我支持你介绍新产品。请问价钱如何？
这个价位貌似没什么优势啊。
补充内容 ( 10:43):
下来看了一下，软件处于开发阶段，相对usbcnc功能太少，离完善还远的很，不适合diy玩家
网站公告 /1
参赛截止时间6月30日
必须有一样
不以此谋生的工作
&&京公网安备
Copyright &
北京木之友文化有限责任公司 All Rights Reserved.involvement of toll-like receptor 2 in experimental invasive pulmonary aspergillosis　
【关键词】& receptor
&&& unite de defense innee et inflammation, inserm e336, institut pasteur, 25, rue du dr roux, 75015 paris, france&&& department of host defense, research institute for microbial diseases, osaka university, osaka, japan&&& unite des aspergillus, institut pasteur, 25, rue du dr roux, 75015 paris, franc&&& unite de bacteriologie moleculaire et medicale, institut pasteur, 28, rue du dr roux, 75015, paris, france&&& unite de recherche et d'expertise histotechnologie et pathologie, institut pasteur, 25, rue du dr roux, 75015 paris, france
&&& abstract
&&& aspergillus fumigatus, an opportunistic fungal pathogen, causes severe and usually fatal invasive pulmonary aspergillosis in immunocompromised hosts. interestingly, drosophila cells lacking the toll protein are prone to a. fumigatus infection. in the current study, we looked for the involvement of toll-like receptor 2 (tlr2) in the recognition of a. fumigatus by analyzing the in vivo and ex vivo responses of immunocompromised tlr2 /
and tlr2+/+ mice to this fungus. upon intratracheal administration of conidia, survival and tumor necrosis factor alpha (tnf-), interleukin-12, and macrophage inhibitory protein-2 alpha concentrations in the airspaces of tlr2 /
mice were significantly lower than those of tlr2+/+ animals. in vitro analysis of tnf- production by conidia-challenged alveolar macrophages from tlr2 /
revealed a significant deficiency in comparison with macrophages from tlr2+/+ mice. infected tlr2 /
mice also have a higher respiratory distress and a higher pathogen burden than tlr2+/+ mice. these data demonstrate that tlr2 plays a significant role in the defense of the host against a. fumigatus infection.
&&& introduction
&&& aspergillus fumigatus is recognized as the most prevalent airborne fungal pathogen and causes severe and usually fatal invasive pulmonary aspergillosis (ipa) in immunocompromised hosts. ipa has become a leading cause of death, due to an increasing number of immunocompromised patients and an increase in the severity of immunosuppressive therapies. classical risk factors are corticotherapy, cytotoxic chemotherapy, and transplantation accompanied by immunosuppressive therapy, and neutropenia remains the most important predisposing factor. available data indicate that the major armaments of host defense against ipa belong to the innate immune system (for a review, see references 13, 18, 19, 30, and 33), such as alveolar macrophages and recruited neutrophils (1, 32).
&&& these two cell types of leukocytes that constitute the first line of defense of the host are able to sense invading microorganisms through different types of receptors, especially through the newly described family of toll-like receptors (tlr) (3, 16, 17, 40, 42). scrutiny of the human and mouse genomes has revealed the existence of not less than 10 different tlr. these receptors are involved in the recognition of various microbe-derived patterns of molecules. early studies have focused on the role played by tlr2 and tlr4 and on their archetypal ligands, i.e., lipoproteins and lipoteichoic acid from gram-positive bacteria on the one hand and lipopolysaccharides from gram-negative bacteria on the other hand. to date, many other ligands have been identified for tlr2 and tlr4, as well as for tlr3, tlr5, tlr7, tlr8, and tlr9 (for a review, see references 3, 16, 17, 40, and 42). all appear key receptors of the innate immune system as their activation initiates a signaling cascade leading to nf-b nuclear translocation and the induction of different proinflammatory genes (3, 16, 17, 40, 42). thus, tlr appear to be directly involved in the fight of infections. for instance, tlr2-deficient mice show higher susceptibility than wild-type mice to infection by the gram-positive bacteria staphylococcus aureus (38) or streptococcus pneumoniae (15). more importantly, it has been reported that a mutation in the tlr2 gene may predispose human beings to life-threatening bacterial infections (23).
&&& interestingly enough, in a pioneering work, lemaitre et al. (21) reported that the toll protein (after which the name tlr was coined) in drosophila is implicated in the defense against a. fumigatus. the fact that drosophila toll protein is activated during fungal or gram-positive infections (22) led us to postulate that tlr2 along with gram-positive bacteria may sense a. fumigatus and as such may play a protective role in ipa. this hypothesis was supported by two early observations, i.e., (i) tlr2 is also activated by zymosan, a yeast cell wall component (41), and (ii) there is a suspicion of an involvement of tlr2 in a model of chronic fungal asthma (4). since then, several in vitro studies using cells from the myeloid lineage have shown that tlr2 is involved in the sensing of a. fumigatus (5, 24, 27, 28). taking advantage of mice genetically deficient in tlr2 (39), the present study analyzes the role of tlr2 in ipa by specifically evaluating in vivo responses in detail and in vitro responses of alveolar macrophages.
&&& materials and methods
&&& materials. ketamine was from merial (lyon, france), xylazine and enrofloxacin from bayer (puteaux, france), tetracycline hydrochloride from roussel diamant (paris-la defense, france), and vinblastine from lilly (saint-cloud, france). for culture medium, fetal calf serum (fcs) was purchased from hyclone (logan, ut) and penicillin and streptomycin from gibco (paisley, united kingdom). acetylacetone was from sigma-aldrich (saint-quentin fallavier, france). finally, d-glucosaminohydrochloride and 4-(dimethylamino)-benzaldehyde were both from merck (darmstadt, germany). kits for the immunoenzymatic detection of the galactomannan antigen of a. fumigatus were obtained from bio-rad (marnes la coquette, france).
&&& preparation of a. fumigatus conidia. a clinical isolate of a. fumigatus (green strain cbs 144.89) was maintained on 2% malt extract agar slants at 22°c. conidia were recovered from cultures grown for 7 days by washing the slant culture with a phosphate-buffered saline (pbs)-0.1% tween 20 solution and gently scraping. conidia were then washed by centrifugation (5 min at 10,000 x g) and suspended in a pbs-0.1% tween 20 solution. conidium concentrations were evaluated by measurement of the optical density of the suspension at 600 nm, with a 0.6 optical density corresponding to 2 x 107 conidia/ml. the suspension was then diluted in order to allow the delivery to mice of the desired concentration under a 50-μl volume.
&&& animal experiments. homozygous mutant mice for tlr2 (tlr2 / ) generated by gene targeting as described previously (39) were back-crossed eight times with c57bl/6 to ensure a similar genetic background. tlr2+/+ homozygous littermates were also back-crossed eight times with c57bl/6. for the establishment of the experimental model of ipa, and for the backcross, 7-week-old c57bl/6 mice were provided by the centre d'elevage r. janvier, le genest saint-isle, france. for the in vivo experiments, 7-week-old male mice were depleted of neutrophils by an intravenous administration of the antineoplastic agent vinblastine (5 mg/kg of body weight) 66 h before infection (1). at the time of conidium administration, depletion of blood-circulating neutrophils was 100% and remained as such for 48 h. mice were given drinking water ad libitum containing 50 μg/ml tetracycline hydrochloride during 4 days before infection. then, 6 h before infection and every 24 h thereafter, mice were administered by the subcutaneous route 0.25 mg enrofloxacin. mice were cared for in accordance with pasteur institute guidelines in compliance with european animal welfare regulation. for intratracheal administration, antibiotic-treated mice were anesthetized by intramuscular administration of 1 mg ketamine and 0.2 mg xylazine and were placed supine. a catheter (diameter of 0.86 mm) was inserted into the trachea via the oropharynx. the proper insertion was verified by checking the formation of mist due to expiration on a mirror placed in front of the external end. a 50-μl conidium suspension was laid down at the internal end of the catheter with a micropipette using a sterile disposable tip for gel loading that was introduced into the catheter. mice were then immediately held upright in order to facilitate conidia inhalation and until normal breathing resumed. this protocol allowed highly reproducible infection of the whole lung (personal data).
&&& assessment of the basal respiratory function. conscious mice were placed in a whole-body barometric plethysmographic chamber (buxco electronics, sharon, ct) to analyze their basal respiratory capacity over time. the system measures both the magnitude and the slope of the chamber pressure. the basal respiratory capacity of each individual mouse was estimated by recording the enhanced pause pressure expressed as penh according to the manufacturer's instructions and as previously reported (20) and which increase is an indicator of deterioration changes in airway mechanics.
&&& collection of balf and measurement of immunoreactive tnf-, il-12, and mip-2 content. mice were euthanized by the intraperitoneal administration of pentobarbital (12 mg/mouse). tracheas were cannulated, and lungs were washed eight times with 0.5 ml pbs to provide 4 ml of bronchoalveolar lavage fluid (balf). there were no significant differences in the total volume of pbs infused into the lungs or in the volume recovered after the lavage procedure among any experimental groups. cell-free balf obtained after centrifugation (300 x g for 15 min) was used for tumor necrosis factor alpha (tnf-) measurement by an enzyme immunometric assay as previously described (31). interleukin-12 (il-12) and macrophage inhibitory protein-2 alpha (mip-2) were quantified by specific enzyme-linked immunosorbent assay kits from biosource (nivelles, belgium) and r&d system europe (lille, france), respectively.
&&& determination of the in vitro tnf- production by alveolar macrophages. balf were collected from naive tlr2 /
and tlr2+/+ mice and pooled by group. collected cells were counted (coulter electronics, margency, france) and centrifuged at 300 x g for 15 min. cells were resuspended at 106/ml of rpmi 1640 supplemented with 10% fcs and 2 mm glutamine. aliquots of 200 μl were dispensed into 96-well tissue culture plates for a 1-h adhesion step at 37°c. wells were then washed to remove nonadherent cells, and remaining adherent cells (2 x 105/well) were immediately incubated at 37°c with a. fumigatus conidia during 6 h at the microbe to cell ratio of 1:1. culture supernatants were then assayed for tnf- concentrations. it is of note that for the in vitro experiments with alveolar macrophages, swollen conidia were prepared by incubating 106 conidia/ml in rpmi 1640 supplemented with 10% fcs and 2 mm glutamine at 37°c for 2 h. the level of killing of resting conidia by alveolar macrophages in vitro after a 6-h incubation is very low, in the range of 6%. in contrast, swollen conidia are more sensitive to killing than resting conidia (29). for that reason, the in vitro activation of alveolar macrophages by a. fumigatus was investigated using swollen conidia.
&&& histology. lungs, kidneys, liver, brain, and spleen were collected at 24 and 48 h after intratracheal infection with 3 x 106 conidia. organs were fixed in 3.7% neutral-buffered formaldehyde, embedded in paraffin, and cut into 5-μm-thick sections. sections were then stained with hematoxylin-eosin stain for tissue examination and with methenamine silver for fungus detection according to the method of sinha et al. (35). upon light microscopic examination, conidia and hyphae were counted on 10 different sections per lung mouse at a magnification of x1,000. one hyphus was defined as a filamentous structure whose length was >10 μm, including a branching structure which derived from a maternal hyphus. by contrast, transversal sections of hyphae as well as conidia were not included. accordingly, the total count of 30 fields at a magnification of x1,000 allowed us to compare the ability to develop germinative structures from conidia considered to be the pathogenic form of the fungus.
&&& measurement of chitin in lungs. lungs and kidneys of mice were homogenized in 5 ml distilled water containing 0.05% tween 20, frozen, and then lyophilized. the preparations were hydrolyzed in 1 ml hcl (8 n) and heated at 100°c for 4 h. reaction was neutralized by the addition of 1 ml naoh (8 n). samples were centrifuged (1,500 x g, 10 min, 20°c). standards consisting of 200 μl glucosamine (50 to 200 μg/ml h2o) or 200 μl of supernatant from each tissue preparation were added to 200 μl buffer containing 25 volumes na2co3 (1.5 m) and 1 volume acetylacetone (4%) heated at 100°c for 20 min and cooled in water. a total of 1.4 ml of ethanol 95% was added. a fresh solution of 4-(dimethylamino)-benzaldehyde (1.6 g in 60 ml hcl and 95% [vol/vol] ethanol) was made, and 200 μl was added to each tube. optical density was measured at 520 nm after 45 min. chitin content was measured in glucosamine equivalents (14).
&&& measurement of galactomannan in lungs and blood. galactomannan antigen (34, 36) was detected by means of a commercially available kit. serum samples were treated as recommended by the manufacturer. for the quantification of galactomannan in lung tissues, aliquots (300 μl) of lung homogenates prepared for the chitin assay were centrifuged at 1,500 x g for 10 min at 4°c and galactomannan concentration was evaluated in supernatants as for serum. the ratio of absorbance sample/absorbance threshold serum was calculated for each test point. then, ratio values were converted in concentrations expressed in ng/ml by considering the ratio value of 1 as being a concentration of 1 ng/ml, as recommended by the manufacturer.
&&& statistical analysis. survival data were analyzed by means of log-rank comparisons of kaplan-meier survival curves, followed by the wilcoxon test using jmp 5.0 software (sas, cary, nc). other results are expressed as means ± standard errors of the means (sem). differences between the data were analyzed by student's unpaired t test. a p value of <0.05 was considered significant.
&&& results
&&& mortality following intratracheal administration of a. fumigatus conidia. we first analyzed the survival of immunocompetent and vinblastine-immunocompromised c57bl/6 mice upon intratracheal administration of conidia from a. fumigatus. vinblastine treatment induced a sustained neutropenia (1, 20) which has for consequence a reduced innate host defense against the fungi (32). upon administration of 106 conidia, all vinblastine-treated mice survived. by contrast, when 107 conidia were given, all immunocompromised mice died within 3 days while all the immunocompetent ones survived long term. neutropenia induced by the antigranulocyte antibody rb6-8c5 (8) has the same consequences in terms of animal survival (data not shown).
&&& having established the model, two groups of either tlr2 /
or tlr2+/+ mice, both immunocompromised upon vinblastine treatment, were challenged with 3 x 106 conidia, an intermediate concentration leading to around 25% mortality in tlr2+/+ animals. as shown in fig. 1, around 50% of tlr2 /
animals were dead by day 4 and only around 30% survived by the end of the experiment (up to day 12). in contrast, only around 10% of tlr2+/+ mice were dead at day 4 and almost 80% of them survived up to the end of the experiment. the wilcoxon test for comparisons of kaplan-meier survival curves indicates a significant decrease in survival in tlr2 /
mice (p = 0.0005). it is of note that immunocompetent tlr2 /
mice (not treated with vinblastine) challenged with a. fumigatus as well as vinblastine-immunocompromised tlr2 /
mice but not challenged with the fungus did not die.
&&& analysis of the tnf-, il-12 and mip-2 in balf and of the in vitro tnf- production by alveolar macrophages incubated with conidia. tnf-, il-12, and mip-2 concentrations were quantified in the balf 24 h after the intratracheal administration of 3 x 106 conidia or their vehicle. as shown in fig. 2, a. fumigatus triggered the synthesis of the three tested mediators but the recovered concentrations were significantly reduced in tlr2 /
compared to tlr2+/+ mice.
&&& alveolar macrophages collected from either tlr2 /
or tlr2+/+ nave mice were incubated for 6 h in the presence or absence of swollen conidia at a 1/1 ratio. this resulted in the induction of tnf- synthesis for both cell types. nonetheless, this induction was significantly reduced for tlr2 /
compared to tlr2+/+ macrophages (fig. 3). it is of note that whether alveolar macrophages were collected from nave or vinblastine-treated mice, they did not differ in their capacity to produce tnf- in response to conidia (data not shown).
&&& assessment of the basal respiratory function. analysis of the basal respiratory function of infected mice showed a significant difference between the two groups as early as 6 h after conidium administration, with penh values of 0.82 ± 0.07 and 0.51 ± 0.09 (n = 4; p < 0.05) for tlr2 /
and tlr2+/+, respectively. these data indicated that the pulmonary infection by a. fumigatus triggers a significant respiratory distress only in the absence of tlr2, as penh values for uninfected tlr2 /
and tlr2+/+ mice were 0.60 ± 0.06 (n = 4) and 0.52 ± 0.06 (n = 4), respectively.
&&& analysis of the pathogen growth. no conidia or hyphae were observed upon microscopic examination in kidneys, liver, brain, or spleen either at 24 h or at 48 h after conidium administration. as expected, conidia and hyphae were present in lungs at 24 h but with no apparent difference between tlr2 /
and tlr2+/+ mice. analysis of the lungs from both tlr2 /
and tlr2+/+ mice at 48 h (fig. 4) showed diffuse and plurifocal lesions of bronchiolitis with segmental destruction of the bronchiolar wall and perivascular involvement. some foci of necrosis were seen around the bronchi and the vessels in both groups, but the lesions of bronchiolitis and necrosis appeared to be more severe in infected tlr2 /
mice than in infected tlr2+/+ mice (fig. 4a to d). there were a few infiltrates characterized by few or no pol macrophages and lymphocytes were observed around the bronchi and the vessels. silver staining (gomori-grocott procedure) revealed typical features of experimental ipa (fig. 4e and f). it especially allowed us to observe that the fungal infection mainly colocalized with the necrotic areas by comparison of silver (fig. 4e and f) and hematoxylin-eosin (fig. 4a and b) stainings. a higher magnification of the silver-stained sections (fig. 4g and h) evidenced numerous hyphae within the parenchyma. counting revealed a higher number of hyphae in tlr2 /
than in tlr2+/+ mice, with values of 13.1 ± 0.7 versus 10.8 ± 0.6 per section (means ± sem of 30 sect p < 0.05), respectively. to obtain another quantification of the invasive hyphal form of a. fumigatus, we evaluated the lung burden of chitin, a component of the hyphal wall that is absent from mammalian cells. significant differences were observed at 24 and 48 h between the two groups of mice, with the highest values of chitin (in glucosamine equivalents) being found in infected tlr2 /
mice (fig. 5). moreover, the concentration of galactomannan, which is released by the growing fungus, was evaluated in lungs and blood at 24 and 48 h (fig. 5). except for the blood at 24 h, higher significant concentrations were found in tlr2 /
than in tlr2+/+ mice.
&&& discussion
&&& the present data demonstrate the participation of tlr2 to the host defense against the opportunistic fungus a. fumigatus. the strongest evidence is given by the survival difference between tlr2 /
and tlr2+/+ mice upon induction of ipa. we also analyzed the production of tnf- by tlr2 /
mice. indeed, tnf- is one of the main cytokines produced by cells of the macrophage lineage after tlr2 activation (10, 39) and is a critical primary mediator in the initiation of pulmonary innate immunity in experimental pneumonia (12, 17). moreover, it is known that tnf- production is crucial for the regulation of ipa, as its neutralization by specific blocking antibodies in an experimental murine model results in an increased mortality associated with an increased fungal burden (26). this may be also relevant for the human pathology as two reports indicated that a clinical treatment with an anti-tnf- antibody is associated with ipa (9, 44). as a result, we observed that the lack of tlr2 apparently renders alveolar macrophages less responsive to a. fumigatus. indeed, tnf- production was reduced in tlr2 /
compared to tlr2+/+ both in vivo and in vitro. along with tnf- production, we also detected reduced concentrations of il-12, a cytokine required for the optimal development of antifungal immunity in mice with ipa (7), and of mip-2, a ligand of cxcr2 which plays an essential role in host defense against a. fumigatus (25). thus, a tlr2-mediated responsiveness of macrophages, and also most probably of other resident cells such as epithelial and dendritic cells, is susceptible to account for the control of the lung infection by a. fumigatus as attested by (i) the observation of a larger number of hyphae in lungs, (ii) the presence of a larger amount of chitin in lungs, and (iii) the detection of a higher concentration of galactomannan in the lungs and serum of tlr2 /
compared to tlr2+/+ mice. interestingly, our findings are consistent with those of a previous study showing that tnf- production by a. fumigatus-challenged peritoneal macrophages (24) and lungs (2) from myd88 /
mice is almost absent, myd88 being a critical adaptor molecule for the intracellular signal transduction induced by the tlr family (3, 16, 37, 40, 42).
&&& nonetheless, activation of alveolar macrophages did not display an all-or-nothing pattern in that some tnf- (i) was recovered from balf of tlr2 /
infected mice and (ii) was also produced in vitro by tlr2 /
macrophages activated by conidia. the anticipated explanation is that in addition to tlr2, other tlr participate in the defense against a. fumigatus. indeed, it is likely that different components of the microorganism are recognized by distinct receptors, most probably along with tlr2 and at least by tlr4. in a pioneering work, it has been shown that specific tlr4-blocking antibodies inhibit, although modestly, the release of tnf- from human monocytes activated by hyphal fragments (43). however, in another study, it has been demonstrated that conidia do not induce nf-b activation in tlr4-transfected hek293 cells but that they do when cells are transfected with tlr2 (24). in fair agreement with our findings, this latter study also showed that elicited peritoneal macrophages from tlr2 /
compared to those of wild-type mice produce less tnf- following a. fumigatus stimulation (24). interestingly, innate defense against a. fumigatus may involve a collaborative activation of tlr2 and dectin-1, a receptor for -glucans which are carbohydrates expressed by a. fumigatus (19). indeed, tlr2 and dectin-1 are synergistic in mediating the production of cytokines such as tnf- and il-12 (6, 11).
&&& regardless, different reports demonstrated the importance of both tlr2 and tlr4 at least in vitro using either murine peritoneal macrophages, bone-marrow-derived dendritic cells, tlr-transfected cells, or human blood mononuclear cells (5, 27, 28). by contrast, our investigation is the first to our knowledge to clearly establish in vivo a role for tlr2 in an experimental murine model of ipa. it is of note, however, that during the course of our study, bellocchio et al. (2) reported in vivo data showing that tlr4 /
mice died sooner than tlr2 /
mice that died like wild-type mice. although there are no apparent explanations for the discrepancies concerning the role of tlr2 between this last study and the other above-mentioned studies and our present work, bellochio et al. (2) nonetheless showed a significantly higher infection of the lungs of tlr2 /
mice than of the lungs of wild-type mice and an enhanced susceptibility of tlr2 /
mice to a secondary challenge with a. fumigatus.
&&& in conclusion, our study shows that tlr2 plays a significant role in a murine model of experimental ipa. it remains to establish the nature of the pathogen-associated molecular pattern(s) expressed by a. fumigatus that triggers the activation of the tlr2-associated signaling pathway leading to the induction of the innate immune response.
&&& acknowledgments
&&& this work was supported in part by a programme transversal de recherche (#94) from the pasteur institute and by a grant from vaincre la mucoviscidose.
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