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Diabetes, Vol 43, Issue 2 329-336, Copyright © 1994 by American Diabetes Association
Islet amyloid polypeptide in human insulinomas. Evidence for intracellular amyloidogenesis
TD O'Brien, AE Butler, PC Roche, KH Johnson and PC Butler
Endocrine Research Unit, Mayo Clinic, Rochester 55905.
Amyloid deposits that characteristically form in the pancreatic islets of
patients with non-insulin-dependent diabetes mellitus (NIDDM) and in
insulinomas are both derived from islet amyloid polypeptide (IAPP).
Evidence from previous studies has suggested that deposition of
IAPP-derived amyloid is related to inherent amyloidogenic sequences present
within normal human IAPP, together with an increased production and local
concentration of IAPP. However, whether the aggregation of IAPP to form
amyloid fibrils is primarily an intra- or extracellular event is not clear.
To address this question, we studied 20 human insulinomas by light and
electron microscopy. By light microscopy, amyloid deposits were
demonstrated in 13 of 20 (65%) human insulinomas. Furthermore, evaluation
of Congo red-stained tumor sections showed small, globular or irregular,
congophilic amyloid deposits within the cytoplasm of many tumor cells in 10
of 13 (77%) amyloid-containing insulinomas. Dense, punctate areas of IAPP
immunoreactivity within tumor cells corresponded with the congophilic
intracellular deposits. Ubiquitin immunoreactivity also was observed as
punctate intracellular labeling and within large extracellular amyloid
deposits. Among the 10 insulinomas available for electron microscopic
evaluation, pathological IAPP-immunoreactive (immunogold) deposits were
found in 3 of 5 insulinomas in which amyloid was demonstrated by light
microscopy and in none of 5 tumors found negative for amyloid by light
microscopy. Morphology of IAPP-immunoreactive deposits varied from those
with the classical distinct 7- to 10-nm diameter nonbranching fibrils to
those with distinct but faint fibrillarity to those without discernable
fibrils.(ABSTRACT TRUNCATED AT 250 WORDS)

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Copyright © 1994 by the American Diabetes Association.
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