|
|
||||||||
Departments of 1 Surgery
2 Physiology and Biophysics
3 Section of Hematology Research
4 Department of Biochemistry and Molecular Biology, Mayo Clinic College of Medicine, Rochester, Minnesota.
5 National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina.
Address correspondence to Virginia M. Miller, PhD, Department of Surgery, Physiology and Biophysics, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, MN 55905. E-mail: miller.virginia{at}mayo.edu
Estrogen receptor beta (ßER) is the predominant estrogen receptor in platelets. Experiments were designed to define phenotypic changes in platelets with aging following deletion of ßER (ßERKO). Blood was collected from wild-type and ßERKO female mice at 47 (young) and 2425 (aged) months of age. In young animals, total number of platelets, number of platelets containing RNA (reticulated platelets), aggregation, dense body adenosine triphosphate secretion, and alpha granular secretion were the same in both groups. With aging, total number of platelets decreased but reticulated platelets increased in ßERKO mice; aggregation and dense granule adenosine triphosphate secretion decreased whereas basal expression of fibrinogen receptors increased with age in wild-type and ßERKO mice. Basal expression of P-selectin and annexin V binding increased with aging only in ßERKO mice; thrombin did not increase expression in these mice. Therefore, deletion of ßER is associated with specific platelet functions, which are expressed only with age-associated reproductive senescence.
HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
---|
All GSA journals | The Gerontologist |
Journals of Gerontology Series B: Psychological Sciences and Social Sciences |