Abstract
The goal of this study is to develop a noninvasive method of SPECT imaging to quantify and stage liver fibrosis with an Asialoglycoprotein receptor (ASGP-R) targeting tracer—99mTc-p(VLA-co-VNI). ASGP-Rs are well known to specifically express in the mammalian liver. Here, we demonstrated ASGP-R expression decreased in carbon tetrachloride (CCl4)-induced mouse model. ASGP-R expression correlated with liver fibrosis progression. ASGP-R could be a useful marker in the stage of liver fibrosis. Liver uptake value (LUV) derived by SPECT imaging was used to assess liver fibrosis in the CCl4-induced mouse model. LUV = [radioactivity (liver uptake)/radioactivity (injected)] × 100/liver volume. The LUV decreased along with the disease progression. The relationships between LUV and liver hydroxyproline (i.e. collagen), as well as Sirius Red were established and verified. A strong negative linear correlation was found between LUV and hydroxyproline levels (r = −0.83) as well as LUV and Sirius Red quantification (r = −0.83). In conclusion, SPECT imaging with 99mTc-p(VLA-co-VNI) is useful in evaluating and staging liver fibrosis in vivo.
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Introduction
Liver fibrosis is the result of repeated liver damage which causes the sustaining activation of tissue repair mechanisms to substitute extracellular matrix (ECM) for necrotic tissue1. In the developed countries, alcohol abuse, chronic HCV infection, and nonalcoholic steatohepatitis (NASH) are the main causes of liver fibrosis. Historically, hepatic fibrosis was thought to be a non-reversible process due to the collapse of the hepatic parenchyma and replacement by a collagenous scar2. Currently, it is considered a reversible compensatory measure response to chronic hepatic injury. However, if it is left unchecked and doesn’t execute positive intervention, fibrosis will progress to cirrhosis. The major clinical consequences of cirrhosis are damage of liver function and development to hepatocellular carcinoma (HCC), both of which is associated with short survival. Moreover, morbidity and mortality are high for patients with severe liver fibrosis operating liver resection3,4.
Liver biopsy is considered as the gold-standard method for the assessment of liver fibrosis despite several limitations5. Histological examination is useful in identifying the leading cause of liver disease and the stage of fibrosis. However, liver biopsy is an invasive procedure with pain. Complications occur in 0.5% of patients, with mortality rates of 5.1%6,7. In addition, histological examination does not predict progression of fibrosis. More remarkable, fibrosis progression before and after transplantation has prognostic significance: serious fibrosis and early cirrhosis are associated with poor survival in patient8,9. Lack of clinical trials is because it requires long-term follow-studies to confirm patients’ condition. However, liver biopsy, an invasive procedure, is still the gold-standard method for identifying the stage of liver fibrosis. Reiterant biopsies to evaluate fibrosis progression or response to treatment are unprepossessing, due to the patient compliance and increased risk of complications. For all of these reasons, there is an urgent need to develop non-invasive ways, which can repeatedly diagnosis of chronic liver disease and monitor fibrosis progression throughout the whole organ, and this will facilitate the design of clinical trials. Unfortunately, mild to moderate stages of liver fibrosis were unable to be detected by conventional imaging although the development of elastography has shown promise in recent years10.
Asialoglycoprotein receptors (ASGP-Rs) which are located on the surface of hepatocytes membrane, are well known to specifically express in the mammalian liver and played a major role in the hepatic metabolism of serum proteins11. For patients with chronic liver disease, ASGP-Rs decrease sharply in liver12,13. Quantitative imaging of ASGP-Rs can assess the function of the liver and provided a noninvasive way to diagnose disease. The ASGP-R imaging agent can assess the anatomy and function of the liver and help the early diagnosis of hepatic diseases and accurate evaluation of functional status14,15. 99mTc-GSA which is an albumin ramification has been used as an ASGP-R-binding radiopharmaceutical in clinical research in Japan since 199216,17,18. In 2011, Yang et al. developed a new synthetic copolymer-p(VLA-co-VNI) with galactose-carrying monomer on the skeleton of styrene and incorporating hydrazine-nicotinamide as functionalized groups for 99mTc labeling as potential ASGP-R imaging agent19. In 2014, Liu et al. synthesized copolymer 99mTc-p(VLA-co-VNI)(46:54) with different ratio of targeting unit (galactose-carrying monomer VLA) and labeling unit (HYNIC-carrying monomer VNI) copolymer with better hepatic targeting and biological properties20. Here, we proved that in vivo SPECT/CT imaging of ASGP-Rs with 99mTc-p(VLA-co-VNI) can reliably distinguish among different stages of liver fibrosis in the CCl4-induced liver fibrosis mouse model and establish a simplified quantification method to assess hepatic fibrosis progression.
Results
Histological characterization of the fibrotic liver in the CCl4-induced mouse model
For the purpose of identifying whether 99mTc-p(VLA-co-VNI) could distinguish early stages of liver fibrosis from more advanced stages, we treated mice with CCl4 or olive oil (as vehicle control) for 4, 8 or 12 weeks to induce varying stages of liver fibrosis. Liver fibrosis progressed in a stepwise fashion in the CCl4 mouse model, as was expected and verified by Sirius Red and H&E staining (Fig. 1A). After 4 weeks of CCl4 administration, most mice had fibrous portal expansion with short fibrous septa (Ishak 2–3), and the disease progressed to complete bridging fibrosis with appearance of a few of regenerative nodules (Ishak 4–5) by 8–12 weeks. Consistently, we detected collagen of liver tissue by hydroxyproline analysis and collagen deposition increased along with the Ishak score (Fig. 1B). We also quantified the amount of collagen deposition by calculating the total amount of Sirius Red staining in representative slides from each animal and this measurement correlated well with Ishak score (Fig. 1C) and liver hydroxyproline levels (Fig. 1D).
ASGP-R expression decreased in CCl4-induced mouse model of liver fibrosis
To determine whether chronic liver injure could down-regulate ASGP-R expression in the CCl4-induced mouse model, we extracted proteins from the liver tissue of control and fibrotic mice to assess the expression of ASGP-R. Western bolt analysis indicated that the protein level of ASGP-R was down-regulated in the liver of fibrotic mice treated with CCl4 (Fig. 2A,B). Down-regulation of ASGP-R expression in the fibrotic mice was further confirmed by immunohistochemical experiment (Supplementary Fig. S1). We observed strong correlations between ASGP-R expression and total collagen levels (r = 0.89, Fig. 2C) as well as ASGP-R expression and Sirius Red quantification (r = 0.82, Fig. 2D). These results indicated that ASGP-R could act as a potential molecular marker in staging of liver fibrosis.
SPECT/CT imaging evaluated the stage of liver fibrosis in a CCl4-induced liver fibrosis mouse model
99 mTc-p(VLA-co-VNI) SPECT/CT imaging was used to quantify asialoglycoprotein receptor expression and assess hepatic fibrosis in mice. LUV derived from SPECT/CT imaging was used as a simplified quantification index to quantify asialoglycoprotein receptor expression and assess the stage of liver fibrosis. LUV was calculated by dividing the liver ROI by the total inject radioactivity and liver volume. The time-activity curve of LUV derived from the dynamic SPECT imaging (Supplementary Fig. S2) showed that the liver uptake in the C57BL/6 mice peaked within 35–50 min after injection. So the static microSPECT scans were performed at 40 min after 99mTc-p(VLA-co-VNI) injection, as seen in Fig. 3A. Strong contrast between the liver and non-targeted tissues or organs was obtained. SPECT/CT image showed specific and obvious high uptake in liver, except for metabolite in intestines and bladder. The specific binding of 99mTc-p(VLA-co-VNI) has been performed previously via blocking experiment of biodistribution, liver uptake decreased significantly by blocking with excess amount of cold p(VLA-co-VNI)20. 99mTc-p(VLA-co-VNI) could specifically target ASGP-R that was further confirmed by the competitive inhibition experiment (Supplementary Fig. S3). The LUV decreased with disease progression (Ishak score) in the fibrotic CCl4-induced mice, as shown in Fig. 3B. LUV of control (Ishak 0) and fibrotic (Ishak 2–3 and Ishak 4–5) mice was 25.5 ± 1.58, 19.0 ± 2.12, and 14.3 ± 2.41, respectively. There have strong correlations between LUV and Sirius Red quantification (r = 0.89, Fig. 3C) and between LUV and liver hydroxyproline levels (r = 0.83, Fig. 3D). We also observed a high correlation between LUV and MMP-9 mRNA relative expression (r = 0. 78, Fig. 3F). The relationship of LUV derived from SPECT imaging by using 99mTc-p(VLA-co-VNI) and 99mTc-GSA respectively was compared as well (r = 0.87, Fig. 3E). Both agents of 99mTc-p(VLA-co-VNI) and 99mTc-GSA for SPECT imaging were obtained with high RCP (>95%) (Supplementary Fig. S4).
Compare the performance of LUV, HH15 and LHL15 in predicting severe hepatic fibrosis
The clearance index HH15 and the receptor index LHL15 are simple indicators used for assessment of blood clearance and hepatic functional reserve. HH15 and LHL15 were calculated by two point data points from the time-activity curves. In order to obtain the liver function indices of LHL15 and HH15, a SPECT/CT dynamic imaging were performed for 15 min with 99mTc-p(VLA-co-VNI). Dynamic imaging of control (Ishak 0) and fibrotic (Ishak 5) mice showed the liver images at 3, 8 and 15 min, as seen in Fig. 4A. Radioactive uptake curve of control (Ishak 0) and fibrotic (Ishak 5) mice showed the liver and heart uptake value (Fig. 4B). In both of normal and fibrotic mice, liver uptake increases over time, whereas radioactivity in blood decreased rapidly. The liver uptake of fibrotic mice is much higher than that of control group and the blood clearance of fibrotic mice is faster than control group (Ishak 0 liver vs. Ishak 5 liver, P < 0.01; Ishak 0 heart vs. Ishak 5 heart, P < 0.05). We present the ROC curves for each of the 3 variables (Fig. 4C). The AUC values of LUV, LHL15 and HH15 for predicting severe liver fibrosis were 0.91, 0.88, and 0.81, respectively. LUV had significantly better performance for predicting severe fibrosis than LHL15 and HH15 (LUV vs. HH15, P < 0.01; LUV vs. LHL15, P < 0.05).
Monitor the therapeutic efficacy of liver fibrosis by SPECT imaging after Tan IIA treatment
The lack of a non-invasive way for evaluating liver fibrosis and monitoring fibrosis progression is the main limitation in the development of anti-fibrotic drugs21. An assessment method based on SPECT imaging with 99mTc-p(VLA-co-VNI) was investigated to monitor the therapeutic efficacy of liver fibrosis. Tan IIA was as potential drug for treatment of liver fibrosis, because it has multiple pharmacological activities, such as anti-oxidant22, anti-inflammatory23. As seen in Fig. 5A,B, Tan IIA had improved liver function as the extent of fibrosis assessed by Sirius Red staining. Moreover, histologic analysis of the Sirius Red staining results demonstrated that the Ishak score improved by approximately two points in the mice after Tan IIA treatment (Fig. 5C). 99mTc-p(VLA-co-VNI) SPECT/CT static imaging showed higher liver uptake in the Tan IIA treatment group compared to the untreated group (Fig. 5E). In the Tan IIA treated group, LUV increased about twice more than control group (Fig. 5F) that correlated with the Sirius Red staining and hydroxyproline analysis (Fig. 5D). These results suggested 99mTc-p(VLA-co-VNI) SPECT/CT imaging could be used as an important method for monitoring fibrosis progression and evaluating the effect of anti-fibrotic drugs.
Discussion
Liver fibrosis is a reversible compensatory measure substitute necrotic hepatocytes with collagen scar. ASGP-Rs, which only express on mammalian hepatocytes, decrease in the progression of liver fibrosis24. We found strong negative correlations between ASGP-R expression and total collagen levels in the fibrotic liver in mice. We wanted to used SPECT/CT imaging with 99mTc-p(VLA-co-VNI) to distinguish among different stages of liver fibrosis and proved it in the CCl4-induced liver fibrosis mouse model. Results obtained from planar 99mTc-GSA scintigraphy are valuable for assessment of liver function in patients with liver damage25,26,27. However, 99mTc-GSA has underlying immunogenicity and there is a risk of viral breakthrough for the blood products of HSA. Moreover, those ASGP-R imaging agents using albumin as backbone have long circulation time in blood, which is not to the advantage of imaging in liver disease. Previously, our research group developed synthetic copolymer p(VLA-co-VNI) as a new ASGP-R agent. p(VLA-co-VNI) uses PVLA as the backbone with galactose-carrying monomer on the skeleton of styrene and incorporates hydrazine-nicotinamide as functionalized groups, which can be rapid clearance from the bloodstream and specific accumulation in the liver.
Although there were many different values calculated from different dynamical models28,29, they are too complex to widely use in the clinical setting. Hepatic receptor index and blood clearance index (LHL15, HH15) are the most simply and commonly used indexes in planar dynamic scintigraphy. However, they may be not sufficient for precise assessment of hepatic functional reserve in liver diseases, because measurement of functional remaining liver volume on planar images obtained by scintigraphy is not accurate. We estimated LUV in the light of the liver uptake density reported by Sugahara30. As a SPECT analysis, it does not need continuous dynamic scan immediately after probe injected. This value is simple, convenient and reproducible. The combined SPECT/CT method gets accurate anatomic data on LUV, and the functional information is attenuated and scatter corrected upon CT images. As it is reported31,32,33, quantification of attenuated and scatter-corrected SPECT images in accordance with CT are more accurate than that based on SPECT images lack of attenuation and scatter correction. In this study, we compared the performance of HH15, LHL15, and LUV in predicting liver fibrosis. The ROC analyses showed that LUV was more accurate than LHL15 for predicting severe fibrosis. Therefore, SPECT/CT fusion images are beneficial to accurate assessment of liver fibrosis.
Here we showed for the first time that 99mTc-p(VLA-co-VNI) SPECT/CT fusion imaging could precisely monitor and stage liver fibrosis progression in CCl4-treated mice. Furthermore, we observed a remarkable correlation between LUV and total collagen levels. 99mTc-p(VLA-co-VNI) SPECT/CT imaging demonstrated LUV was reduced by 45% in the severe fibrosis mice compared to the control group. However, even in the severe fibrotic mice, the fibrotic area accounted for only 3.7% of the whole liver assessed by Sirius Red staining. Therefore, the decrease of LUV would not be as a result of substitute ECM for necrotic tissue in the fibrotic mice. Western analysis indicated that the protein level of ASGP-R was down-regulated approximate 50% in the liver of severe fibrotic mice correlated with the change of LUV. All of above results suggested LUV decrease was result from alterations of ASGP-R expression rather than collagen deposition. And then we observed a remarkable correlation between ASGP-R expression and total collagen levels. Therefore, it is viable to monitor progression of the fibrosis by quantifying ASGP-R expression and assessing hepatic functional reserve. Though histologic examination is useful in identifying the potential cause of liver diseases and evaluating the inflammatory grade and the stage of fibrosis, histological scoring suffers from the limitation of biopsy and only represents a very small sample of the whole liver. Therefore, 99mTc-p(VLA-co-VNI) SPECT/CT imaging of the entire liver might better represent disease stage than histological scoring of biopsied liver tissue.
Further study is needed to determine whether 99mTc-p(VLA-co-VNI) SPECT/CT imaging can be used to monitor fibrosis progression in response to treatment. Removing the causative agent is the most effective intervention in the treatment of liver fibrosis. However, in some case, it is difficult to remove the insulting agent of liver diseases (for example, HCV and fatty liver). We used Tan IIA for treatment of liver fibrosis, just because of multiple pharmacological activities of Tan IIA, such as anti-oxidant, anti-inflammatory. As it is reported, the inflammatory factors (e.g., IL-1β, IL-6, SOCS1, and IFN-γ) facilitate the activation of HSC and promote the fibrotic progression34,35,36 and genes mediating ROS generation (e.g., NADPH oxidase) regulate both inflammation and ECM deposition37. The results of our study suggest that treatment with Tan IIA can degrade collagen fibers and reduce liver fibrosis. Increased LUV were observed in Tan IIA treated group in SPECT/CT imaging with 99mTc-p(VLA-co-VNI). Here we report the non-invasive method based on SPECT/CT imaging with 99mTc-p(VLA-co-VNI) can be greater benefit to monitor fibrosis progression and evaluate the efficacy of anti-fibrotic drugs comprehensively.
Several radiotracers targeting other receptors were reported used for noninvasive fibrosis imaging. Muzard et al. described a 99mTc labeled peptidomimetic of the platelet collagen receptor glycoprotein VI by targeting collagen38. The radiotracer was demonstrated to successfully image fibrosis in vivo in a mouse model of lung fibrosis. Yu et al. reported a αvβ3–targeting radiotracer 99mTc-3PRGD239. The radiotracer could identify liver fibrosis as early as 4 weeks after TAA treatment. Compared with these previous radiotracer, 99mTc-p(VLA-co-VNI) showed higher uptake in liver and lower kidney accumulation which was beneficial for the quantification of liver uptake. In our study we defined a simplified quantification index LUV and conducted correlation analysis of LUV with physiological index of liver fibrosis. We demonstrated that SPECT/CT with 99mTc-p(VLA-co-VNI) could reliably distinguish among different stages of liver fibrosis in the CCl4-induced liver fibrosis mouse model. However, 99mTc-p(VLA-co-VNI) as a ASGP-R targeting radiotracer was only useful for detection of liver fibrosis rather than else fibrotic diseases.
In conclusion, 99mTc-p(VLA-co-VNI) SPECT and CT fusion imaging is useful for accurately stage fibrosis and quantitative evaluation the functional reserve of the liver in CCl4-treated mice. The LUV is the most important SPECT/CT value for diagnosing histological liver damage and predicting severe fibrosis. 99mTc-p(VLA-co-VNI) SPECT can be a valuable tool for predicting fibrosis response to therapy and selecting more appropriate treatment regimens for patients with chronic liver disease.
Mehtods
Animal models
The experimental procedures and the animal use and care protocols were approved by the Institutional Animal Care and Use Committee of Xiamen University. All experimental protocols were carried out in accordance with the relevant guidelines. C57BL/6 mice obtained from the Laboratory Animal Center of Xiamen University were administered 0.1 mL of a 40% solution of CCl4 (Sigma, St. Louis, MO) in olive oil by intraperitoneal injection, two times a week for either 4, 8 or 12 weeks, to induce fibrosis at different stages (n = 6 for all time points). Controls received only pure olive oil. Animals were imaged one week after the last injection to avoid acute effects of CCl4. Tanshinone II-A (Tan IIA), the main active diterpene quinone extracted from Salvia miltiorrhiza was used for the treatment of liver fibrosis; One group of mice was administered with 0.1 mL of a 40% solution of CCl4 while another group was administered with 100 mg/kg Tan IIA (added in a same dose CCl4 solution) by intraperitoneal injection, two times a week for 9 weeks (n = 6 for each group).
Probes
The radiolabeling procedure was similar to the previously published literature19,20 Briefly, the optimal proportion of p(VLA-co-VNI)(46:54) lyophilized kit are 1 mg copolymer, 5 mg TPPTS, 6.5 mg Tricine, 12.7 mg succinic acid, 34.5 mg disodium succinate hexahydrate and 40 mg mannitol. For radiolabeling, the sealed kit was added 0.5 mL of freshly eluted 99mTcO4− (60–100 MBq) from a commercial generator (HTA Co. Ltd., China) and heated for 20 min at 100 °C. After reaction, the crude product was passing through a 0.22 μm millipore filter to obtain the resulting complex 99mTc-p(VLA-co-VNI)(46:54)(Tricine)(TPPTS) (shorted as 99mTc-p(VLA-co-VNI)).
99mTc-GSA was obtained by using an instant kit method (lyophilized GSA kits were donated by Beijing Shihong Pharmaceutical Center) for comparison. Briefly, by adding 0.5 mL elution of 99mTcO4− (180–300 MBq) to a GSA kit, followed by incubation at room temperature for 15 min.
Both of the radiochemistry purity (RCP) of 99mTc-p(VLA-co-VNI) and 99mTc-GSA were evaluated by using ITLC/ACD chromatography system (Supplementary materials and methods 1.4).
Western Blot Analysis
Approximately 40 μg total liver tissues’ extracts were estimated using the Bio-Rad protein assay system. Samples were resolved on a 10% SDS-polyacrylamide gel and then transferred to a polyvinylidene difluoride membrane (Millipore, Bedford, MA, USA). After blocking with 10% bovine serum albumin, the blot was incubated with anti-ASGP-R1 antibody (abcam, ab88042; 1:1,000 dilution). Horseradish peroxidase-conjugated secondary antibodies (Sigma, St. Louis, MO, USA) were typically diluted 1:5000 and chemiluminescent substrate (Amersham Pharmacia Biotech, Piscataway, NJ, USA) was used as described in the manufacturer’s instructions.
mRNA quantification
Total RNA was extracted from liver tissues and complementary DNA was synthesized. qPCR for mRNA was performed on a real-time PCR system (CFX96, Bio-Rad, CA, USA). Primers used are listed as follows: MMP9-F: AGG ATG GGA AGT ACT GGC GAT TCT CTG; MMP9-R: ACT TGG TCC ACC TGG TTC AAC TCA CTC and beta-actin-F: GAC CTC TAT GCC AAC ACA GTG C; beta-actin-R: GTA CTC CTG CTT GCT GAT CCA C.
In vivo imaging
SPECT/CT imaging studies were carried out in accordance with the approved guidelines. SPECT/CT imaging was performed using nanoScan SC (Mediso Medical Imaging System) equipped with pinhole collimator under standard animal scan procedure. The CT acquiring parameters were as follows: energy peak of 50 kV, 670 μA, 480 projections, medium zoom. SPECT acquiring parameters were as follows: energy peak of 140 keV for 99mTc, window width of 20%, matrix of 256 × 256, medium zoom, and frame: 30 s. Dynamic SPECT acquiring parameters were as follows: 20 scans, and 30 sec/frame from 0–15 min.
SPECT/CT imaging of normal C57BL/6 mice and fibrotic mice under anesthesia by isoflurane to evaluate the specific binding to ASGP-R were performed with 99mTc-p(VLA-co-VNI). The normal C57BL/6 mice were acquired under anesthesia 40 min after injecting via the tail vein with 18 MBq of 99mTc-p(VLA-co-VNI). The static and dynamic SPECT/CT imaging of hepatic fibrosis mice (control, experiment and Tan IIA treated group) were performed for comparison, respectively.
Calculation of the dynamic data HH15 and LHL15: time-activity curves of the liver and heart were derived from the radioactivity measured in the region of interest (ROI) of the whole liver and radioactivity measured in the ROI of the heart40; the blood clearance index (HH15) was calculated by dividing the radioactivity measured in ROI of the heart at 15 min after injection by the radioactivity measured in ROI of the heart at 3 min41. The receptor index (LHL15) was calculated by dividing the radioactivity of ROI of the liver by the sum of the radioactivity of the liver and heart ROIs at 15 min after injection41−43.
In order to further validate the feasibility of this new developed methodology, SPECT/CT imaging of normal C57BL/6 mice and hepatic fibrosis mice with known agent 99mTc-GSA were also performed for comparison.
Tissue analysis
Paraformaldehyde-fixed samples were embedded in paraffin, cut into 5 μm-thick sections and stained with Sirius Red according to standard procedures. Sirius Red stained sections were analyzed by three pathologists, who were blinded to the study. Fibrosis stage is assessed by using scales of Ishak score. Hydroxyproline in liver tissue was quantified by HPLC analysis according to previous reports44.
Statistics
Results are expressed as mean ± standard error of the mean. Differences among groups were evaluated by one way analysis of variance (ANOVA) followed by a Newman-Keuls post hoc test. The Pearson correlation coefficient was computed to assess quality of linear correlations and significance was evaluated by Two-tailed test. Receiver operating curve (ROC) analysis was performed using Origin 8. Differences were considered significant if P < 0.05.
Additional Information
How to cite this article: Zhang, D. et al. Simplified quantification method for in vivo SPECT/CT imaging of asialoglycoprotein receptor with 99mTc-p(VLA-co-VNI) to assess and stage hepatic fibrosis in mice. Sci. Rep. 6, 25377; doi: 10.1038/srep25377 (2016).
References
Iredale, J. P. Models of liver fibrosis: exploring the dynamic nature of inflammation and repair in a solid organ. J Clin Invest 117, 539–548 (2007).
Albanis, E. & Friedman, S. L. Hepatic fibrosis. Pathogenesis and principles of therapy. Clin Liver Dis 5, 315–334 (2001).
Kaibori, M. et al. HA/GSA-Rmax ratio as a predictor of postoperative liver failure. World J Surg 32, 2410–2418 (2008).
Farges, O. et al. Risk of major liver resection in patients with underlying chronic liver disease: a reappraisal. Ann Surg 229, 210–215 (1999).
Manning, D. S. & Afdhal, N. H. Diagnosis and quantitation of fibrosis. Gastroenterology 134, 1670–1681 (2008).
Myers, R. P., Fong, A. & Shaheen A. A. Utilization rates, complications and costs of percutaneous liver biopsy: a population-based study including 4275 biopsies. Liver Int 28, 705–712 (2008).
Terjung, B. et al. Bleeding complications after percutaneous liver biopsy. An analysis of risk factors. Digestion 67, 138–145 (2003).
Poynard, T., Bedossa, P. & Opolon, P. Natural history of liver fibrosis progression in patients with chronic hepatitis C. The OBSVIRC, METAVIR, CLINIVIR, and DOSVIRC groups. Lancet 349, 825–832 (1997).
Forman, L. M. et al. The association between hepatitis C infection and survival after orthotopic liver transplantation. Gastroenterology 122, 889–896 (2002).
Afdhal, N. H. & Nunes, D. Evaluation of liver fibrosis: a concise review. Am J Gastroenterol 99, 1160–1174 (2004).
Hoekstra, L. T. et al. Physiological and biochemical basis of clinical liver function tests: a review. Ann Surg 257, 27–36 (2013).
Marshall, J. S. et al. Measurement of circulating desialylated glycoproteins and correlation with hepatocellular damage. J Clin Invest 54, 555–562 (1974).
Sawamura, T. et al. Decrease of a hepatic binding protein specific for asialoglycoproteins with accumulation of serum asialoglycoproteins in galactosamine-treated rats. Gastroenterology 81, 527–533 (1981).
Du, S. et al. A novel liver function evaluation system using radiopharmacokinetic modeling of technetium-99m-DTPA-galactosyl human serum albumin. Nucl Med Commun 34, 893–899 (2013).
Stadalnik, R. C. & Vera, D. R. The evolution of 99mTc-NGA as a clinically useful receptor-binding radiopharmaceutical. Nucl Med Biol 28, 499–503 (2001).
Kwon, A. et al. Preoperative determination of the surgical procedure for hepatectomy using technetium-99 mgalactosyl human serum albumin (99mTc-GSA) liver scintigraphy. Hepatology 25, 426–429 (1997).
Mao, Y. et al. Using Dynamic 99mTc-GSA SPECT/CT fusion images for hepatectomy planning and postoperative liver failure prediction. Ann Surg Oncol 22, 1301–1307 (2015).
Sugahara, K. et al. Separate analysis of asialoglycoprotein receptors in the right and left hepatic lobes using 99mTc-GSA SPECT. Hepatology 38, 1401–1409 (2003).
Yang, W. et al. Copolymer-based hepatocytes asialoglycoprotein receptor targeting agent for SPECT. J Nucl Med 52, 978–985 (2011).
Liu, C. et al. Kit formulated asialoglycoprotein receptor targeting tracer based on copolymer for liver SPECT imaging. Nucl Med Biol 41, 587–593 (2014).
Popov, Y. & Schuppan, D. Targeting liver fibrosis: strategies for development and validation of antifibrotic therapies. Hepatology 50, 1294–1306 (2009).
Fu, J. et al. Tanshinone IIA protects cardiac myocytes against oxidative stress-triggered damage and apoptosis. Eur J Phar 568, 213–221 (2007).
Li, Q. et al. Novel polymeric nanoparticles containing tanshinone IIA for the treatment of hepatoma. J Drug Tar 16, 725–732 (2008).
Afdhal, N. H. & Nunes, D. Evaluation of liver fibrosis: a concise review. Am J Gastroenterol 99, 1160–1174 (2004).
Kim, E. M. et al. Asialoglycoproteinreceptor-targeted hepatocyte imaging using 99mTc galactosylated chitosan. Nucl Med Biol 33, 529–534 (2006).
Sasaki, N. et al. Clinical usefulness of scintigraphy with 99mTc-galactosyl-human serum albumin for prognosis of cirrhosis of the liver. J Nucl Med 40, 1652–1656 (1999).
Kira, T. et al. Correlation of 99mTc-GSA hepatic scintigraphy with liver biopsies in patients with chronic active hepatitis type C. Radiat Med 17, 125–130 (1999).
Vera, D. R. et al. Measurement of receptor concentration and forward-binding rate constant via radiopharmacokinetic modeling of technetium-99m-galactosyl-neoglycoalbumin. J Nucl Med 32, 1169–1176 (1991).
Yang, W., Mou, T., Zhang, X. & Wang, X. Synthesis and biological evaluation of 99mTc-DMP-NGA as a novel hepatic asialoglycoprotein receptor imaging agent. Appl Radiat Isot 68, 105–109 (2010).
Zeintl, J. et al. Quantitative accuracy of clinical 99mTc SPECT/CT using ordered-subset expectation maximization with 3-dimensional resolution recovery, attenuation, and scatter correction. J Nucl Med 51, 921–928 (2010).
Seo, Y. et al. Correction of photon attenuation and collimator response for a body-contouring SPECT/CT imaging system. J Nucl Med 46, 868–877 (2005).
Kashiwagi, T. et al. Correction of nonuniform attenuation and image fusion in SPECT imaging by means of separate X-ray CT. Ann Nucl Med 16, 255–261 (2002).
Wong, V. S. et al. Serum hyaluronic acid is a useful marker of liver fibrosis in chronic hepatitis C virus infection. J Viral Hepat 5, 187–192 (1998).
Yoshida, T. et al. SOCS1 is a suppressor of liver fibrosis and hepatitis-induced carcinogenesis. J Exp Med 199, 1701–1707 (2004).
Streetz, K. L. et al. Interleukin 6/gp130-dependent pathways are protective during chronic liver diseases. Hepatology 38, 218–229 (2004).
Sahai, A. et al. Upregulation of osteopontin expression is involved in the development of nonalcoholic steatohepatitis in a dietary murine model. Am J Physiol Gastrointest Liver Physiol 287, G264–G273 (2004).
Bataller, R. et al. NADPH oxidase signal transduces angiotensin II in hepatic stellate cells and is critical in hepatic fibrosis. J Clin Invest 112, 1383–1394 (2003).
Muzard, J. et al. Non-invasive molecular imaging of fibrosis using a collagen-targeted peptidomimetic of the platelet collagen receptor glycoprotein VI. PLoS One 4, e5585 (2009).
Yu, X. et al. Small-animal SPECT/CT of the progression and recovery of rat liver fibrosis by using an integrin αvβ3-targeting radiotracer. Radiology 14, 150090 (2015).
Mitsumori, A. et al. Preoperative evaluation of hepatic functional reserve following hepatectomy by technetium-99m galactosyl human serum albumin liver scintigraphy and computed tomography. Eur J Nucl Med 25, 1377–1382 (1998).
Kwon, A. H. et al. Preoperative regional maximal removal rate of technetium-99m-galactosyl human serum albumin (GSA-Rmax) is useful for judging the safety of hepatic resection. Surgery 117, 429–434 (1995).
Kokudo, N., Vera D. R. & Makuuchi, M. Clinical application of TcGSA. Nucl Med Biol 30, 845–849 (2003).
Tanaka, A. et al. Perioperative changes in hepatic function as assessed by asialoglycoprotein receptor indices by technetium-99m galactosyl human serum albumin. Hepatogastroenterology 46, 369–375 (1999).
Hutson P. R., Crawford M. E. & Sorkness R. L. Liquid chromatographic determination of hydroxyproline in tissue samples. J Chromatogr B Analyt Technol Biomed Life Sci 791, 427–430 (2003).
Acknowledgements
The project was sponsored by the National Key Basic Research Program of China (2014CB744503) and National Natural Science Foundation of China (81471707, 21271030), and partially by the Fundamental Research Funds for the Central Universities of China (20720150063, 2013SH009).
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X.Z. conceived and designed the experiments; D.Z. performed the data analyses and wrote the manuscript; D.Z., Z.G. and Y.L. contributed significantly to analysis and manuscript preparation; P.Z., X.S. and H.W. helped perform the analysis with constructive discussions; L.Y. and M.G. contributed significantly to establishment of the animal models; C.L. contributed to the synthesis of the SPECT imaging tracer.
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Zhang, D., Guo, Z., Zhang, P. et al. Simplified quantification method for in vivo SPECT/CT imaging of asialoglycoprotein receptor with 99mTc-p(VLA-co-VNI) to assess and stage hepatic fibrosis in mice. Sci Rep 6, 25377 (2016). https://doi.org/10.1038/srep25377
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DOI: https://doi.org/10.1038/srep25377
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