Immunoreactivity for Ano1 detects depletion of Kit-positive interstitial cells of Cajal in patients with slow transit constipation.
Immunoreactivity for Ano1 detects depletion of Kit-positive interstitial cells of Cajal in patients with slow transit constipation.
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DOI:
10.1111/j.1365-2982.2011.01729.x
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发表时间:
2011-08
影响因子:
3.5
通讯作者:
Farrugia G
中科院分区:
文献类型:
--
作者:
Kashyap P;Gomez-Pinilla PJ;Pozo MJ;Cima RR;Dozois EJ;Larson DW;Ordog T;Gibbons SJ;Farrugia G
Depletion of interstitial cells of Cajal (ICC) is associated with several gastrointestinal motility disorders. Changes in ICC networks are usually detected by immunolabeling for the receptor tyrosine kinase Kit. Ano1 (DOG1 or TMEM16A) was recently described as a marker of ICC in gastrointestinal tract. Our aim was to determine whether Ano1-immunoreactivity can be used as a reliable marker for ICC in tissues from patients with motility disorders. Four tissues from patients with normal ICC numbers and four tissues from patients with slow transit constipation and loss of Kit-positive ICC were studied. ICC were detected by double labeling using antisera to Kit and Ano1. Both the processes and cell bodies of ICC in tissue from controls and slow transit constipation were immunoreactive for Ano1. There was near complete overlap between Kit and Ano1 immunoreactivity. Tissues from patients with slow transit constipation contained significantly fewer Ano1-positive ICC than control tissues. The numbers of ICC identified by Ano1 and Kit-immunoreactivity were nearly identical across the range of ICC numbers from an average of 1.64 to 7.05 cells per field and correlated with an R2 value of 0.99. Ano1 is a reliable and sensitive marker for detecting changes in ICC networks in humans. Labeling with antibodies selective for Ano1 reproducibly detects depletion of Kit-positive ICC in tissues from patients with slow transit constipation.
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影响因子:
5.5
作者:
Davis, Alison J.;Forrest, Abigail S.;Leblanc, Normand
通讯作者:
Leblanc, Normand
影响因子:
29.4
作者:
Lorincz, Andrea;Redelman, Doug;Ordog, Tamas
通讯作者:
Ordog, Tamas
影响因子:
29.4
作者:
He, CL;Burgart, L;Farrugia, G
通讯作者:
Farrugia, G
影响因子:
3.6
作者:
TORIHASHI, S;WARD, SM;SANDERS, KM
通讯作者:
SANDERS, KM
影响因子:
24.5
作者:
Lyford, GL;He, CL;Farrugia, G
通讯作者:
Farrugia, G