Decreased pancreatic acinar cell number in type 1 diabetes.


Journal

Diabetologia
ISSN: 1432-0428
Titre abrégé: Diabetologia
Pays: Germany
ID NLM: 0006777

Informations de publication

Date de publication:
07 2020
Historique:
received: 13 11 2019
accepted: 20 03 2020
pubmed: 11 5 2020
medline: 5 10 2021
entrez: 11 5 2020
Statut: ppublish

Résumé

Individuals with longstanding and recent-onset type 1 diabetes have a smaller pancreas. Since beta cells represent a very small portion of the pancreas, the loss of pancreas volume in diabetes is primarily due to the loss of pancreatic exocrine mass. However, the structural changes in the exocrine pancreas in diabetes are not well understood. To characterise the pancreatic endocrine and exocrine compartments in diabetes, we studied pancreases from adult donors with type 1 diabetes compared with similarly aged donors without diabetes. Islet cell mass, islet morphometry, exocrine mass, acinar cell size and number and pancreas fibrosis were assessed by immunohistochemical staining. To better understand possible mechanisms of altered pancreas size, we measured pancreas size in three mouse models of insulin deficiency. Pancreases from donors with type 1 diabetes were approximately 45% smaller than those from donors without diabetes (47.4 ± 2.6 vs 85.7 ± 3.7 g), independent of diabetes duration or age of onset. Diabetic donor pancreases had decreased beta cell mass (0.061 ± 0.025 vs 0.94 ± 0.21 g) and reduced total exocrine mass (42.0 ± 4.9 vs 96.1 ± 6.5 g). Diabetic acinar cells were similar in size but fewer in number compared with those in pancreases from non-diabetic donors (63.7 ± 8.1 × 10 Pancreases from donors with type 1 diabetes are smaller than normal donor pancreases because exocrine cells are fewer in number rather than smaller in size; these changes occur early in the disease process. Our mouse data suggest that decreased pancreas size in type 1 diabetes is not directly caused by insulin deficiency, but the precise mechanism responsible remains unclear.

Identifiants

pubmed: 32388592
doi: 10.1007/s00125-020-05155-y
pii: 10.1007/s00125-020-05155-y
pmc: PMC8403487
mid: NIHMS1592868
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

1418-1423

Subventions

Organisme : NIDDK NIH HHS
ID : T32 DK007061
Pays : United States
Organisme : NIDDK NIH HHS
ID : P60 DK020593
Pays : United States
Organisme : NIDDK NIH HHS
ID : UC4 DK104211
Pays : United States
Organisme : NIH HHS
ID : OD020351
Pays : United States
Organisme : NIDDK NIH HHS
ID : UC4 DK108120
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK072473
Pays : United States
Organisme : NIDDK NIH HHS
ID : R29 DK046266
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK095735
Pays : United States
Organisme : NIDDK NIH HHS
ID : R24 DK106755
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK097829
Pays : United States
Organisme : NIH HHS
ID : U54 OD020351
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK112217
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK046266
Pays : United States
Organisme : NIDDK NIH HHS
ID : UC4 DK112232
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK089572
Pays : United States
Organisme : U.S. Department of Veterans Affairs
ID : BX000666
Pays : International
Organisme : BLRD VA
ID : I01 BX000666
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK094199
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK020593
Pays : United States

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Auteurs

Jordan J Wright (JJ)

Division of Diabetes, Endocrinology, and Metabolism, Department of Medicine, Vanderbilt University Medical Center, 7465 Medical Research Bldg IV, 2215 Garland Avenue, Nashville, TN, 37232-0475, USA.

Diane C Saunders (DC)

Division of Diabetes, Endocrinology, and Metabolism, Department of Medicine, Vanderbilt University Medical Center, 7465 Medical Research Bldg IV, 2215 Garland Avenue, Nashville, TN, 37232-0475, USA.

Chunhua Dai (C)

Division of Diabetes, Endocrinology, and Metabolism, Department of Medicine, Vanderbilt University Medical Center, 7465 Medical Research Bldg IV, 2215 Garland Avenue, Nashville, TN, 37232-0475, USA.

Greg Poffenberger (G)

Division of Diabetes, Endocrinology, and Metabolism, Department of Medicine, Vanderbilt University Medical Center, 7465 Medical Research Bldg IV, 2215 Garland Avenue, Nashville, TN, 37232-0475, USA.

Brynn Cairns (B)

The Jackson Laboratory, Bar Harbor, ME, USA.

David V Serreze (DV)

The Jackson Laboratory, Bar Harbor, ME, USA.

David M Harlan (DM)

Division of Diabetes, Department of Medicine, Diabetes Center of Excellence, University of Massachusetts Medical School, Worcester, MA, USA.

Rita Bottino (R)

Institute of Cellular Therapeutics, Allegheny-Singer Research Institute Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA, USA.

Marcela Brissova (M)

Division of Diabetes, Endocrinology, and Metabolism, Department of Medicine, Vanderbilt University Medical Center, 7465 Medical Research Bldg IV, 2215 Garland Avenue, Nashville, TN, 37232-0475, USA. marcela.brissova@vumc.org.

Alvin C Powers (AC)

Division of Diabetes, Endocrinology, and Metabolism, Department of Medicine, Vanderbilt University Medical Center, 7465 Medical Research Bldg IV, 2215 Garland Avenue, Nashville, TN, 37232-0475, USA. al.powers@vumc.org.
Deparment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, USA. al.powers@vumc.org.
Veterans Affairs Tennessee Valley Healthcare System, Nashville, TN, USA. al.powers@vumc.org.

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Classifications MeSH