Literature DB >> 16813956

In vivo detection of apoptotic cells in the testis using fluorescence labeled annexin V in a mouse model of testicular torsion.

Sang-Kuk Yang1, Sharon Attipoe, Adam P Klausner, Rong Tian, Dongfeng Pan, Tyvin A Rich, Terry T Turner, William D Steers, Jeffrey J Lysiak.   

Abstract

PURPOSE: It is well established that experimental testicular torsion induces germ cell specific apoptosis. Annexin V (BD Pharmingentrade mark) binds phosphatidylserine that becomes exposed on the cell membrane in apoptotic cells. In vivo detection of apoptotic cells with fluorescently labeled annexin V is an emerging technique that we evaluated for detecting apoptotic germ cells in a mouse model of testicular torsion.
MATERIALS AND METHODS: Annexin V labeled with an indocyanine fluorophore (bisfunctional succinimidyl ester of cyanine 5.5) (Amersham, Little Chalfont, United Kingdom) was injected intravenously in mice 18 hours after the repair of unilateral 720-degree testicular torsion for 2 hours. Serial fluorescence images were obtained 21, 24, 28 and 42 hours after torsion repair. Relative fluorophore localization was visualized in vivo using an optical small animal imaging system mounted with a filter in near infrared light. Average fluorescence intensity in torsed and sham testes was quantified in images of testes in situ exposed through an abdominal incision and in ex vivo testes.
RESULTS: A significant increase in fluorescence intensity was found in images of torsed vs sham operated testes. This was seen in ex vivo, exposed and in vivo testes (215%, 250% and 161%, respectively, p <0.05). Bisfunctional succinimidyl ester of cyanine 5.5 conjugated to dehydrogenase, a protein with a size similar to that of annexin V, was used to assess for capillary leakage. It was also more localized to the torsed testis relative to its contralateral sham control whether exposed or ex vivo (174% and 176%, respectively).
CONCLUSIONS: To our knowledge this study demonstrates for the first time the possibility of in vivo near infrared fluorescence imaging of apoptotic germ cells after testicular torsion in mice. It shows important confounding factors that must be considered as this new imaging technique is developed for detecting apoptotic cells in vivo in testes or in any other organ.

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Year:  2006        PMID: 16813956     DOI: 10.1016/j.juro.2006.03.073

Source DB:  PubMed          Journal:  J Urol        ISSN: 0022-5347            Impact factor:   7.450


  4 in total

1.  In vivo cell death mediated by synthetic ion channels.

Authors:  Bryan A Smith; Megan M Daschbach; Seth T Gammon; Shuzhang Xiao; Sarah E Chapman; Caroline Hudson; Mark Suckow; David Piwnica-Worms; George W Gokel; W Matthew Leevy
Journal:  Chem Commun (Camb)       Date:  2011-06-17       Impact factor: 6.222

2.  Detection of myocardial ischemia-reperfusion injury using a fluorescent near-infrared zinc(II)-dipicolylamine probe and 99mTc glucarate.

Authors:  Leonie Wyffels; Brian D Gray; Christy Barber; Koon Y Pak; Safiyyah Forbes; Jeffrey A Mattis; James M Woolfenden; Zhonglin Liu
Journal:  Mol Imaging       Date:  2012-06       Impact factor: 4.488

Review 3.  Clearance of apoptotic cells: implications in health and disease.

Authors:  Michael R Elliott; Kodi S Ravichandran
Journal:  J Cell Biol       Date:  2010-06-28       Impact factor: 10.539

4.  Potential targets for molecular imaging of apoptosis resistance in hepatocellular carcinoma.

Authors:  Z Liu; M Cheng; Mz Cao
Journal:  Biomed Imaging Interv J       Date:  2011-01-01
  4 in total

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