Pharmacokinetics of the phosphatidylserine tracers 99mTc-lactadherin and 99mTc-annexin V in pigs
© Poulsen et al.; licensee Springer. 2013
Received: 31 October 2012
Accepted: 18 February 2013
Published: 9 March 2013
Phosphatidylserine (PS) is a phospholipid normally located in the inner leaflet of the cell membrane. PS is translocated from the inner to the outer leaflet of the plasma membrane during the early stages of apoptosis and in necrosis. In cell and animal studies, reversible PS externalisation to the outer membrane leaflet has been observed in viable cells. Hence, PS markers have been proposed as markers of both reversibly and irreversibly damaged cells. The purpose of this experimental study in pigs was to investigate the kinetics of the newly introduced PS marker technetium-99m-labelled lactadherin (99mTc-lactadherin) in comparison with the well-known PS tracer 99mTc-annexin V with special reference to the renal handling of the tracers. The effective dose for humans was estimated from the biodistribution in 24 mice.
Nine anaesthetised pigs randomly allocated into two treatment groups were administered a single injection of either 99mTc-lactadherin or 99mTc-annexin V. Renal perfusion was assessed by simultaneous injection of 51Cr-EDTA. Throughout the examinations, planar, dynamic scintigraphy of the trunk was performed, urine was collected and arterial and renal vein blood was sampled. The effective dose was estimated using the adult male phantom from the RADAR website.
99mTc-lactadherin was cleared four times faster from plasma than 99mTc-annexin V, 57 ± 13 ml/min (mean ± SD) versus 14 ± 2 ml/min. 99mTc-lactadherin had a predominant uptake in the liver, whereas 99mTc-annexin V was primarily taken up by the kidneys. The estimated effective human dose after single injection of 99mTc-lactadherin and 99mTc-annexin V was 5.8 and 11 μSv/MBq, respectively.
The high hepatic uptake of 99mTc-lactadherin compromises the use of 99mTc-lactadherin for imaging PS externalisation in the liver. Due to scatter from the liver, the use of in vivo visualisation of PS externalisation in the lower thorax and upper abdomen by 99mTc-lactadherin is challenged, but not precluded. In contrast to 99mTc-annexin, 99mTc-lactadherin has a low renal uptake and may be the preferred tracer for imaging PS externalisation in the kidneys. The effective dose after injection of 99mTc-lactadherin and 99mTc-annexin was low. Recommendations regarding the clinical use of 99mTc-lactadherin must await tracer kinetic studies in patients.
Phosphatidylserine (PS) is a phospholipid normally located in the inner leaflet of the cell membrane. PS is translocated from the inner to the outer leaflet of the plasma membrane during the early stages of apoptosis and in necrosis [1, 2]. In cell and animal studies, reversible PS externalisation to the outer membrane leaflet has been observed in viable cells [3–5]. Hence, PS markers have been proposed as indicators of damaged cells, whether reversibly or irreversibly injured [6–8].
Fluorescent or radio isotope-labelled annexin V is frequently used to visualise the externalisation of PS on the cell surface [4, 9, 10]. Recently, the glycoprotein lactadherin (also known as MFG-E8) was introduced as a more sensitive PS marker [11, 12], and the technetium-99m-labelled lactadherin (99mTc-lactadherin) has been proven to readily visualise PS externalisation on cells .
The binding affinity of annexin V and lactadherin to cells with decreasing transmembrane potential is increased . Since the membrane of apoptotic, hypoxic and ischemic cells depolarised, annexin V and lactadherin most likely bind to these cells with a higher affinity than to cells with preserved membrane potential.
The PS externalisation on dying cells is described as an ‘eat me’ signal to the macrophages that mediate engulfment . Lactadherin facilitates this phagocytosis by acting as a bridge between exposed PS and the αvβ3 integrin on the macrophage surface . It is well known that the inflammatory response to cell death is minimised when dying cells are effectively removed. A more direct anti-inflammatory effect of lactadherin has been demonstrated ex vivo by Voll et al. . They showed that lactadherin increases the secession of anti-inflammatory cytokines from the macrophage. In experimental studies of inflamed and ischemic tissues, lactadherin is described as an organ-protecting component [18–20].
Given the promising future of lactadherin, both in diagnostic imaging and for anti-inflammatory treatment, knowledge of the kinetics of the compound is highly relevant.
The purpose of the present pharmacokinetic study in pigs was to compare the kinetics of 99mTc-lactadherin with that of 99mTc-annexin V with special reference to the renal handling. Further, the aim was to estimate an effective human dose by the use of data from an earlier biodistribution study in mice .
Animal preparation and experimental protocol
The study was approved by the Danish Inspectorate of Animal Experimentation and performed in accordance with their guidelines.
Nine female Danish Landrace/Yorkshire pigs, weighing 20 kg, were premedicated with midazolam 3 mg/kg (Dormicum®, Roche, Basel, Switzerland) and s-ketamine (S-Ketamin, Pfizer Aps, Ballerup, Denmark) subcutaneously. Subsequently, the pigs received a 375 mg bolus of pentobarbital (Mebumal®, DAK, Copenhagen, Denmark) in an auricular vein and were intubated and ventilated (Datex Ohmeda s/5 Avance ventilator, GE Healthcare, Little Chalfront, UK). During the entire data collection, anaesthesia was maintained by sevoflurane (Sevorane 100%, Abbotte Scandinavia AB, Solna, Sweden).
The arterial blood gases, pH, blood glucose and electrolytes were frequently monitored (ABL, Radiometer A/S, Brønshøj, Denmark), and ventilation was adjusted to keep the blood gases in physiological ranges. An intravenous saline infusion was maintained at a rate of approximately 200 ml · h−1. Temperature was registered with a rectal probe and was kept between 38°C and 39°C, which is the physiological range of temperature for pigs of this size. An appropriate environmental temperature was applied during transportation from the farm and during the study. If necessary, blankets and/or fans were used to maintain a steady, physiologic temperature.
A kidney vein catheter for venous blood samples was inserted through a sheath in the femoral vein. Since kidney vein blood has a higher oxygenation than mixed venous blood, the position of the catheter was assured by comparing the oxygen saturation in the kidney and jugular vein blood drawn simultaneously. Blood samples were drawn slowly from the kidney vein catheter to avoid aspiration of mixed venous blood from the inferior cava vein.
Arterial blood sampling and blood pressure measurement were performed through a sheath in the femoral artery. Heart rate and blood pressure were continuously monitored to ensure hemodynamic stability. A sheath was also inserted in the right internal jugular vein for tracer administration and saline infusion. The urinary bladder was catheterized and the urine collected.
The preparation time from the induction of anaesthesia to tracer injection was approximately 80 min.
Tracer preparation and administration
The radio synthesis of 99mTc-lactadherin and 99mTc-annexin V has been described previously [13, 21]. Five pigs received an injection dose (ID) of 19 to 38 MBq 99mTc-lactadherin (99mTc-hynic-lactadherin, Department of Nuclear Medicine, Denmark), and four pigs received 25 to 37 MBq 99mTc-annexin V (99mTc-hynic-recombinant human (rh)-annexin V, Reactionlab A/S, Lynge, Denmark) bolus in the jugular vein. The effective specific activity of 99mTc-lactadherin and 99mTc-annexin V at the time of injection was approximately 3.1 and 3.7 MBq/μg protein, respectively. The radiochemical purity was over 95% for both tracers. Simultaneously with PS tracer injection, all nine pigs received an intravenous dose of 4 MBq 51Cr-EDTA (Behring, Marburg, Germany) to determine the renal plasma flow (RPF).
Dynamic imaging (64 × 64 matrix) of the trunk in the posterior projection was performed with a single-headed gamma camera (BrightView, Philips Medical, North Andover, MA, USA) equipped with a LEHR collimator. During the first 120 s post-injection (pi.), a frame rate of 1 per second was applied. From 2 to 60 min, the frame rate was 1 per minute, and from 60 min to the end of the study, 1 frame was recorded over 5 min (12 frames per hour).
The biodistribution of the PS tracers was evaluated by studying the tracer activity over time. Representative areas of the heart, lungs, liver, spleen and kidneys were drawn as regions of interest (ROI) on the scintigrams, and time/activity curves were generated. Activity was assessed as counts per minute per pixel and corrected for background radiation measured under the left kidney and for radioactive decay.
This method provides only a semi-quantitative description of tracer uptake in different organs over time, and the method is less suitable for quantitative comparison of tracer uptake between organs. Planar scintigraphy simplifies the three-dimensional tracer distribution to a two-dimensional image. Hence, organ activity assessed from planar images is proportional not only to tracer uptake, but also to the vertical thickness of the organs and the activity in overlying and underlying tissues.
Blood and urine sampling
Blood samples (3 ml) were drawn from the renal vein and the femoral artery 2 min before tracer injection and at 2, 5, 10, 15, 20, 25, 30, 40, 50, 60, 75, 90, 105, 120, 135 and 150 min and then every 30th minute up to 240 min pi. Blood from two pigs, one injected with 99mTc-annexin V and one with 99mTc-lactadherin, were sampled up to only 150 min pi. Urine was collected simultaneously with blood sampling.
Radioisotope activity was counted in 1 ml plasma, 1 ml whole blood and 1 ml urine in a scintillation detector (Cobra II, Packard, Meriden, CT, USA) to a statistical accuracy of 1%. 99mTechnetium activity was counted immediately after the experiment and 51Chromium activity 3 to 10 days later. Correction was made for background radioactive decay and cross-talk between channels.
Whole blood clearance (ClWb), plasma clearance (ClP), volume of distribution (V d), urinary clearance (Clu), renal extraction (E tracer) and fraction of injected dose (ID) excreted in urine were calculated for all three tracers using the data collected from blood and urine samples.
- 2.RPF was calculated using the reference tracer 51Cr-EDTA and the equation
- 3.Renal clearance (Clr-tracer) of annexin and lactadherin was calculated from the equation
The fraction of the tracer retained in the kidneys was calculated as the relative difference in renal clearance (Clr-tracer) and urinary clearance (Clu-tracer) as a fraction of the renal clearance (Clr-tracer).
The area under the time-activity curve was calculated by fitting the time-activity data from the plasma and blood samples with three exponential functions using a peeling-off technique in a computer program (Sigma Plot 11, Systat Software, Chicago, IL, USA). Three exponential functions were used to get a satisfactory data fit. We did not use a compartment model.
Volume of distribution (V d) was assessed from the equation: , where is the mean transit time and Clp is the plasma clearance of the tracer.
where U denotes the concentration of the tracer in the urine and V the volume of urine collected. The product of U and V was divided by the area under the time-activity curve.
The extraction was calculated for each sampling as well as an average value corrected to a mean time.
The fraction of ID excreted in urine is the amount of tracer found in urine divided by the ID.
where Clu-EDTA was used as an estimate of Clr-EDTA . EDTA is excreted solely by glomerular filtration, making Clu-EDTA a good estimate of Clr-EDTA . Mean RPF was calculated for all nine pigs together and separately for pigs receiving either 99mTc-annexin or 99mTc-lactadherin.
Dosimetry calculation on published data
The biodistribution of 99mTc-lactadherin and 99mTc-annexin V has been studied by our group in 24 mice sacrificed at 10, 60, or 180 min pi. . From these data and by the use of the adult male phantom from the RADAR website (USA), an effective radiation dose to the human body after a single injection with the 99mTc-lactadherin or the 99mTc-annexin V compound was assessed.
Results derived from blood and urine samples
Results derived from blood and urine samples
Lactadherin (n = 5)
Annexin (n = 4)
EDTA (n = 9)
Plasma clearance (ml/min)
57 ± 13
14 ± 1.9
42 ± 6.8
Volume of distribution (L)
8.2 ± 3.6
3.3 ± 0.35
6.3 ± 1.2
Urinary clearance (ml/min)
2.4 ± 1.3
1.0 ± 0.37
28 ± 8.07
Renal extraction fraction
0.011 ± 0.004
0.037 ± 0.010
0.21 ± 0.05
Fraction of ID excreted in urine (120/180/240)
Urinary flow (ml/min)
1.7 ± 0.8
2.4 ± 1.4
2.0 ± 1.1
Renal plasma flow (ml/min)
152 ± 62
144 ± 22
148 ± 47
Renal clearance (ml/min)
1.6 ± 0.9
5.3 ± 1.5
Fraction retained in kidneys
−1.10 ± 1.3
0.80 ± 0.10
Effective dose estimated from biodistribution in mice
The effective dose for 99mTc-lactadherin and for 99mTc-annexin V was estimated from previously published data . The biodistribution of 99mTc-lactadherin in mice was found to be 64% in the liver, 4.7% in the kidneys, 12% in the blood and 19% in the remaining body. Effective residence times (worst case values) were estimated as 6, 6, 3.3 and 20 h, respectively. This biodistribution is assumed to be representative for humans, and by using dose factors from the adult male phantom from the RADAR website, the effective dose was estimated to be 5.8 μSv/MBq. The biodistribution of 99mTc-annexin V was found to be 48% in the kidneys, 12% in the liver, 12% in the blood and 28% in the remaining body. Effective residence times (worst case values) were estimated as 6, 6, 4.4 and 18.6 h, respectively. The effective dose was calculated as 8.8 μSv/MBq.
The tracer kinetics of 99mTc-annexin V has been studied in animal models as well as in humans. Clinical studies have shown the ability of 99mTc-annexin V to visualise apoptosis, e.g. the complete or partial tumour response was associated with increased uptake of 99mTc-annexin V [22–24].
99mTc-lactadherin is a newer tracer with a higher affinity for the PS than 99mTc-annexin V. Tracer kinetic studies have been performed only in vitro and in small animals [13, 21]. We have made a comparative study of the kinetics of 99mTc-lactadherin and 99mTc-annexin V in pigs, an animal close to man both regarding the heart and the kidneys.
The present study showed important differences in the kinetics of 99mTc-lactadherin and 99mTc-annexin V. The renal extraction of 99mTc-annexin V was only 3.7%, but 80% was retained in the kidneys and the kidneys were clearly delineated on the scintigrams. The renal clearance of 99mTc-annexin V comprises nearly one third of the plasma clearance. Previous studies have also demonstrated that 99mTc-annexin V was predominantly taken up by the kidney followed by liver and urinary bladder uptake . The reason for the intense kidney accumulation remains unclear, but the uptake seems to be relatively nonspecific and does not alter upon apoptosis induction with cycloheximide in mice . The same authors speculate that the reason might be an organ-specific endocytotic mechanism for annexin V that relies on a non-PS-dependent membrane association. The kidney uptake could have been free 99mTc-pertechnetate. However, we did not see any activity in the thyroid, making this explanation less likely. The vague visualisation of the liver by 99mTc-annexin V corresponded with previous findings , and it may be due only to the blood background.
A different pattern was observed for 99mTc-lactadherin for which we observed a high hepatic uptake and only a minor uptake in the kidneys. The renal extraction of 99mTc-lactadherin was as low as 1% and the renal clearance of 99mTc-lactadherin responding to only 2.8% of the plasma clearance. The rapid and very dominant liver uptake corresponded well to the rapid plasma clearance of 99mTc-lactadherin, the latest being more than four times faster than the plasma clearance of 99mTc-annexin V. The distribution of the two PS tracers in the present study is in concordance with the results from the earlier study in mice .
The dominant liver uptake indicated that 99mTc-lactadherin is either primarily metabolized in or slowly excreted by the liver as we did not observe a decline in the time/activity curve over the liver. Further, no bile ducts or bowl activity was visualised on the scintigrams, indicating that neither the isotope nor the tracer was excreted from the liver to a significant degree during the study periods.
Lactadherin is a glycoprotein identified in mammary glands, but also present in the brain, heart, lungs, spleen, intestines, liver, kidneys, reproductive organs and blood . Notably, endogenously secretion might in many cases be ascribed to tissue-embedded macrophages . This is in concordance with the suggested function of lactadherin, i.e. the glycoprotein operates as a bridging molecule between PS-exposing apoptotic/necrotic cells and integrin receptors on macrophages [16, 29]. What hitherto is known about the nature of lactadherin prescribes that it most likely will be found as a membrane-associated component, especially the ones with high curvature , and suggests that under normal physiological conditions, blood lactadherin will be carried around on cell debris, membrane fragments or microvesicle-like structures. The liver has a well-developed ability to engulf apoptotic cells, involving the action of hepatocytes, Kupffer and endothelial cells . This may explain the presently observed high and rapid liver uptake of 99mTc-lactadherin.
One might argue that the high and rapid liver uptake of 99mTc-lactadherin leaves no compound for targeting PS. However, in an ischemic and reperfused porcine model, we studied the PS externalisation in the myocardium after reperfusion using 99mTc-lactadherin (RH Poulsen et al., unpublished work). A well-defined uptake of 99mTc-lactadherin was found in the part of the myocardium exposed to ischemia and reperfusion, suggesting sufficient amount of 99mTc-lactadherin for PS targeting despite the extensive hepatic uptake.
The effective dose for 99mTc-lactadherin and for 99mTc-annexin V was estimated from previously published data, assuming that the biodistribution in mice is representative for humans. The effective human dose after a single injection of 99mTc-lactadherin was estimated to be 5.8 and 8.8 μSv/MBq for 99mTc-annexin V which is in the clinically acceptable range and comparable to other routinely performed nuclear examinations. In comparison, in humans, the effective dose for 99mTc-annexin V has been found to be 11 μSv/MBq .
51Cr-EDTA was used as a reference substance in order to calculate renal plasma flow to determine renal clearance of 99mTc-lactadherin and 99mTc-annexinV. We found a 51Cr-EDTA renal extraction of 21.6%, which is in concordance with earlier studies in pigs. During the experiment, the renal extraction of 51Cr-EDTA decreased slightly. Unlike humans, pigs have several kidney veins, which are both smaller and shorter than in humans. This makes blood sampling from the renal vein difficult. The concentration of 51Cr-EDTA is higher in the caval vein than in the renal veins, and contamination with caval blood would lead to an underestimation of the renal 51Cr-EDTA extraction. Contamination with blood from the inferior caval vein might explain the observed drop in EDTA excretion.
51Cr-EDTA is known to be excreted solely in the urine. The discrepancy between the plasma and urinary clearance of 51Cr-EDTA represents a bias that can be caused by the different methods used to estimate the two clearances.
The initial renal extraction fraction of 99mTc-annexin V was more than 10% (Figure 3) but decreased to zero during the first 2 h of the experiment. Consequently, the contribution of the kidneys to the total plasma clearance decreased during the study period. On average, the renal extraction fraction of 99mTc-annexin V was 3.7%.
The renal extraction fraction of 99mTc-lactadherin was very close to zero throughout the study period. The amount of 99mTc-lactadherin cleared from the blood on its way through the kidney was therefore very small. We found that the urinary clearance of 99mTc-lactadherin exceeded the renal clearance. This has to be explained from the insignificant kidney excretion and the uncertainty of the measurement.
Overall, the results from the present tracer kinetic study in pigs were in accordance with the findings of recent studies in mice and humans [21, 25]. Choosing a pig model was motivated by the knowledge of its genetic and physiological similarities to humans.
Further studies of the hepatic metabolism of 99mTc-lactadherin are necessary to ensure a full understanding of the kinetic and biodistribution of the tracer. Moreover, it would be highly relevant to study 99mTc-lactadherin's ability to visualise PS externalisation in apoptosis, ischemic or inflammatory experimental models. Finally, an adequate patient dosimetry study of 99mTc-lactadherin is recommended before a potential clinical imaging with 99mTc-lactadherin.
The high hepatic uptake of 99mTc-lactadherin may compromise the use of 99mTc-lactadherin for visualisation of PS externalisation in the liver and in organs close to the liver. In contrast to 99mTc-annexin, 99mTc-lactadherin has a low renal uptake and may be the preferred tracer for imaging PS externalisation in the kidneys. The biodistribution of 99mTc-annexin V favours this tracer as the preferred marker for imaging PS externalisation in the upper abdomen and the lower thorax.
The estimated effective human dose after a single injection of 99mTc-lactadherin is in the clinically acceptable range and comparable to other routinely performed nuclear examinations. However, recommendation regarding the clinical use of 99mTc-lactadherin must await tracer kinetic studies and dosimetry calculations in patients.
We are grateful to Lene E. Nielsen, a medical technician from the Department of Nuclear Medicine, Aarhus University Hospital, Denmark, for her assistance in the conduction of the animal experiments and the analysis of data obtained from samples counted in the scintillation detector. With great gratitude, we received financial support from the Aarhus University Foundation and the Danish Agency for Science Technology and Innovation.
- Krysko O, De RL, Cornelissen M: Phosphatidylserine exposure during early primary necrosis (oncosis) in JB6 cells as evidenced by immunogold labeling technique. Apoptosis 2004, 9: 495–500.View ArticleGoogle Scholar
- Fadok VA, Voelker DR, Campbell PA, Cohen JJ, Bratton DL, Henson PM: Exposure of phosphatidylserine on the surface of apoptotic lymphocytes triggers specific recognition and removal by macrophages. J Immunol 1992, 148: 2207–2216.Google Scholar
- Balasubramanian K, Mirnikjoo B, Schroit AJ: Regulated externalization of phosphatidylserine at the cell surface: implications for apoptosis. J Biol Chem 2007, 282: 18357–18364. 10.1074/jbc.M700202200View ArticleGoogle Scholar
- Kenis H, Zandbergen HR, Hofstra L, Petrov AD, Dumont EA, Blankenberg FD, Haider N, Bitsch N, Gijbels M, Verjans JW, Narula N, Narula J, Reutelingsperger CP: Annexin A5 uptake in ischemic myocardium: demonstration of reversible phosphatidylserine externalization and feasibility of radionuclide imaging. J Nucl Med 2010, 51: 259–267. 10.2967/jnumed.109.068429View ArticleGoogle Scholar
- Mari C, Karabiyikoglu M, Goris ML, Tait JF, Yenari MA, Blankenberg FG: Detection of focal hypoxic-ischemic injury and neuronal stress in a rodent model of unilateral MCA occlusion/reperfusion using radiolabeled annexin V. Eur J Nucl Med Mol Imaging 2004, 31: 733–739. 10.1007/s00259-004-1473-5View ArticleGoogle Scholar
- Blankenberg FG: Imaging the molecular signatures of apoptosis and injury with radiolabeled annexin V. Proc Am Thorac Soc 2009, 6: 469–476. 10.1513/pats.200901-001AWPubMed CentralView ArticleGoogle Scholar
- Taki J, Higuchi T, Kawashima A, Fukuoka M, Kayano D, Tait JF, Matsunari I, Nakajima K, Kinuya S, Strauss HW: Effect of postconditioning on myocardial 99mTc-annexin-V uptake: comparison with ischemic preconditioning and caspase inhibitor treatment. J Nucl Med 2007, 48: 1301–1307. 10.2967/jnumed.106.037408View ArticleGoogle Scholar
- Narula J, Strauss HW: Invited commentary: P.S.* I love you: implications of phosphatidyl serine (PS) reversal in acute ischemic syndromes. J Nucl Med 2003, 44: 397–399.Google Scholar
- Rottey S, Slegers G, Van BS, Goethals I, Van de WC: Sequential 99mTc-hydrazinonicotinamide-annexin V imaging for predicting response to chemotherapy. J Nucl Med 2006, 47: 1813–1818.Google Scholar
- Vangestel C, Van de Wiele C, Van Damme N, Staelens S, Pauwels P, Reutelingsperger CP, Peeters M: (99)mTc-(CO)(3) His-annexin A5 micro-SPECT demonstrates increased cell death by irinotecan during the vascular normalization window caused by bevacizumab. J Nucl Med 2011, 52: 1786–1794. 10.2967/jnumed.111.092650View ArticleGoogle Scholar
- Shi J, Pipe SW, Rasmussen JT, Heegaard CW, Gilbert GE: Lactadherin blocks thrombosis and hemostasis in vivo: correlation with platelet phosphatidylserine exposure. J Thromb Haemost 2008, 6: 1167–1174. 10.1111/j.1538-7836.2008.03010.xView ArticleGoogle Scholar
- Dasgupta SK, Guchhait P, Thiagarajan P: Lactadherin binding and phosphatidylserine expression on cell surface-comparison with annexin A5. Transl Res 2006, 148: 19–25. 10.1016/j.lab.2006.03.006View ArticleGoogle Scholar
- Waehrens LN, Rasmussen JT, Heegaard CW, Faldborg L: Preparation and in vitro evaluation of 99 m-Tc-labelled bovine lactadherin as a novel radioligand for apoptosis detection. J Label Compd Radiopham 2007, 50: 211–217. 10.1002/jlcr.1207View ArticleGoogle Scholar
- Smith C, Gibson DF, Tait JF: Transmembrane voltage regulates binding of annexin V and lactadherin to cells with exposed phosphatidylserine. BMC Biochem 2009, 10: 5. 10.1186/1471-2091-10-5PubMed CentralView ArticleGoogle Scholar
- Hanayama R, Tanaka M, Miwa K, Shinohara A, Iwamatsu A, Nagata S: Identification of a factor that links apoptotic cells to phagocytes. Nature 2002, 417: 182–187. 10.1038/417182aView ArticleGoogle Scholar
- Toda S, Hanayama R, Nagata S: Two-step engulfment of apoptotic cells. Mol Cell Biol 2012, 32: 118–125. 10.1128/MCB.05993-11PubMed CentralView ArticleGoogle Scholar
- Voll RE, Herrmann M, Roth EA, Stach C, Kalden JR, Girkontaite I: Immunosuppressive effects of apoptotic cells. Nature 1997, 390: 350–351. 10.1038/37022View ArticleGoogle Scholar
- Hanayama R, Tanaka M, Miyasaka K, Aozasa K, Koike M, Uchiyama Y, Nagata S: Autoimmune disease and impaired uptake of apoptotic cells in MFG-E8-deficient mice. Science 2004, 304: 1147–1150. 10.1126/science.1094359View ArticleGoogle Scholar
- Cui T, Miksa M, Wu R, Komura H, Zhou M, Dong W, Wang Z, Higuchi S, Chaung W, Blau SA, Marini CP, Ravikumar TS, Wang P: Milk fat globule epidermal growth factor 8 attenuates acute lung injury in mice after intestinal ischemia and reperfusion. Am J Respir Crit Care Med 2010, 181: 238–246. 10.1164/rccm.200804-625OCPubMed CentralView ArticleGoogle Scholar
- Cheyuo C, Jacob A, Wu R, Zhou M, Qi L, Dong W, Ji Y, Chaung WW, Wang H, Nicastro J, Coppa GF, Wang P: Recombinant human MFG-E8 attenuates cerebral ischemic injury: Its role in anti-inflammation and anti-apoptosis. Neuropharmacology 2012, 62: 890–900. 10.1016/j.neuropharm.2011.09.018PubMed CentralView ArticleGoogle Scholar
- Falborg L, Waehrens LN, Alsner J, Bluhme H, Frokiaer J, Heegaard CW, Horsman MR, Rasmussen JT, Rehling M: Biodistribution of 99mTc-HYNIC-lactadherin in mice–a potential tracer for visualizing apoptosis in vivo. Scand J Clin Lab Invest 2010, 70: 209–216. 10.3109/00365511003663648View ArticleGoogle Scholar
- Kartachova M, Haas RL, Olmos RA, Hoebers FJ, van Zandwijk N, Verheij M: In vivo imaging of apoptosis by 99mTc-annexin V scintigraphy: visual analysis in relation to treatment response. Radiother Oncol 2004, 72: 333–339. 10.1016/j.radonc.2004.07.008View ArticleGoogle Scholar
- Kartachova M, an Zandwijk N, Burgers S, van Tinteren H, Verheij M, Valdes Olmos RA: Prognostic significance of 99mTc Hynic-rh-annexin V scintigraphy during platinum-based chemotherapy in advanced lung cancer. J Clin Oncol 2007, 25: 2534–2539. 10.1200/JCO.2006.10.1337View ArticleGoogle Scholar
- Hoebers FJ, Kartachova M, de Bois J, van den Brekel MW, van Tinteren H, van Herk M, Rasch CRN, Valdés Olmos RA, Verheij M: 99mTc Hynic-rh-Annexin V scintigraphy for in vivo imaging of apoptosis in patients with head and neck cancer treated with chemoradiotherapy. Eur J Nucl Med Mol Imaging 2008, 35: 509–518. 10.1007/s00259-007-0624-xPubMed CentralView ArticleGoogle Scholar
- Kemerink GJ, Liu X, Kieffer D, Ceyssens S, Mortelmans L, Verbruggen AM, Steinmetz ND, Vanderheyden JL, Green AM, Verbeke K: Safety, biodistribution, and dosimetry of 99mTc-HYNIC-annexin V, a novel human recombinant annexin V for human application. J Nucl Med 2003, 44: 947–952.Google Scholar
- Tait JF, Smith C, Blankenberg FG: Structural requirements for in vivo detection of cell death with 99mTc-annexin V. J Nucl Med 2005, 46: 807–815.PubMed CentralGoogle Scholar
- Aziz M, Jacob A, Matsuda A, Wang P: Review: milk fat globule-EGF factor 8 expression, function and plausible signal transduction in resolving inflammation. Apoptosis 2011, 16: 1077–1086. 10.1007/s10495-011-0630-0View ArticleGoogle Scholar
- Bu HF, Zuo XL, Wang X, Ensslin MA, Koti V, Hsueh W, Raymond AS, Shur BD, Tan XD: Milk fat globule-EGF factor 8/lactadherin plays a crucial role in maintenance and repair of murine intestinal epithelium. J Clin Invest 2007, 117: 3673–3683.PubMed CentralGoogle Scholar
- Hirt UA, Leist M: Rapid, noninflammatory and PS-dependent phagocytic clearance of necrotic cells. Cell Death Differ 2003, 10: 1156–1164. 10.1038/sj.cdd.4401286View ArticleGoogle Scholar
- Otzen DE, Andersen KK: Folding of outer membrane proteins. Arch Biochem Biophys 2012. 10.1016/j.abb.2012.10.008Google Scholar
- Dini L, Pagliara P, Carla EC: Phagocytosis of apoptotic cells by liver: a morphological study. Microsc Res Tech 2002, 57: 530–540. 10.1002/jemt.10107View ArticleGoogle Scholar
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