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Differential effects of leptin receptor mutation on male and female BBDR.Gimap5-/Gimap5- spontaneously diabetic rats

Moralejo, Daniel H.; Hansen, Carl T.; Treuting, Piper; Hessner, Martin J; Fuller, Jessica M. LU ; Van Yserloo, Brian; Jensen, Richard; Osborne, William; Kwitek, Anne E. and Lernmark, Åke LU (2010) In Physiological Genomics 41(1). p.9-20
Abstract

Rodents homozygous for autosomal leptin receptor gene mutations not only become obese, insulin resistant, and hyperleptinemic but also develop a dysregulated immune system. Using marker-assisted breeding to introgress the Koletsky rat leptin receptor mutant (lepr-/lepr-), we developed a novel congenic BBDR.lepr-/lepr- rat line to study the development of obesity and type 2 diabetes (T2D) in the BioBreeding (BB) diabetesresistant (DR) rat. While heterozygous lepr (-/+) or homozygous (+/+) BBDR rats remained lean and metabolically normal, at 3 wk of age all BBDR.lepr-/lepr- rats were obese without hyperglycemia. Between 45 and 70 days of age, male but not female obese rats developed T2D. We had previously... (More)

Rodents homozygous for autosomal leptin receptor gene mutations not only become obese, insulin resistant, and hyperleptinemic but also develop a dysregulated immune system. Using marker-assisted breeding to introgress the Koletsky rat leptin receptor mutant (lepr-/lepr-), we developed a novel congenic BBDR.lepr-/lepr- rat line to study the development of obesity and type 2 diabetes (T2D) in the BioBreeding (BB) diabetesresistant (DR) rat. While heterozygous lepr (-/+) or homozygous (+/+) BBDR rats remained lean and metabolically normal, at 3 wk of age all BBDR.lepr-/lepr- rats were obese without hyperglycemia. Between 45 and 70 days of age, male but not female obese rats developed T2D. We had previously developed congenic BBDR. Gimap5-/Gimap5-rats, which carry an autosomal frameshift mutation in the Gimap5 gene linked to lymphopenia and spontaneous development of type 1 diabetes (T1D) without sex differences. Because the autoimmune-mediated destruction of pancreatic islet β-cells may be affected not only by obesity but also by the absence of leptin receptor signaling, we next generated BBDR.lepr-/lepr-,Gimap5-/Gimap5- double congenic rats carrying the mutation for Gimap5 and T1D as well as the Lepr mutation for obesity and T2D. The hyperleptinemia rescued end-stage islets in BBDR. lepr-/lepr-,Gimap5-/Gimap5- congenic rats and induced an increase in islet size in both sexes, while T1D development was delayed and reduced only in females. These results demonstrate that obesity and T2D induced by introgression of the Koletsky leptin receptor mutation in the BBDR rat result in islet expansion associated with protection from T1D in female but not male BBDR. lepr-/lepr-,Gimap5-/Gimap5- congenic rats. BBDR. lepr-/lepr-,Gimap5-/Gimap5- congenic rats should prove valuable to study interactions between lack of leptin receptor signaling, obesity, and sex-specific T2D and T1D.

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author
publishing date
type
Contribution to journal
publication status
published
keywords
Diabetes, Islet inflammation, Lymphopenia, Obesity
in
Physiological Genomics
volume
41
issue
1
pages
12 pages
publisher
American Physiological Society
external identifiers
  • scopus:77949660725
ISSN
1094-8341
DOI
10.1152/physiolgenomics.00186.2009
language
English
LU publication?
no
id
fb1c563d-8c89-41b1-a2aa-519d590b8613
date added to LUP
2017-09-07 11:56:56
date last changed
2018-05-29 09:56:34
@article{fb1c563d-8c89-41b1-a2aa-519d590b8613,
  abstract     = {<p>Rodents homozygous for autosomal leptin receptor gene mutations not only become obese, insulin resistant, and hyperleptinemic but also develop a dysregulated immune system. Using marker-assisted breeding to introgress the Koletsky rat leptin receptor mutant (<sup>lepr-/lepr-</sup>), we developed a novel congenic BBDR.<sup>lepr-/lepr-</sup> rat line to study the development of obesity and type 2 diabetes (T2D) in the BioBreeding (BB) diabetesresistant (DR) rat. While heterozygous lepr (-/+) or homozygous (+/+) BBDR rats remained lean and metabolically normal, at 3 wk of age all BBDR.<sup>lepr-/lepr-</sup> rats were obese without hyperglycemia. Between 45 and 70 days of age, male but not female obese rats developed T2D. We had previously developed congenic BBDR. <sup>Gimap5-/Gimap5-</sup>rats, which carry an autosomal frameshift mutation in the Gimap5 gene linked to lymphopenia and spontaneous development of type 1 diabetes (T1D) without sex differences. Because the autoimmune-mediated destruction of pancreatic islet β-cells may be affected not only by obesity but also by the absence of leptin receptor signaling, we next generated BBDR.<sup>lepr-/lepr-,Gimap5-/Gimap5-</sup> double congenic rats carrying the mutation for Gimap5 and T1D as well as the Lepr mutation for obesity and T2D. The hyperleptinemia rescued end-stage islets in BBDR. <sup>lepr-/lepr-,Gimap5-/Gimap5-</sup> congenic rats and induced an increase in islet size in both sexes, while T1D development was delayed and reduced only in females. These results demonstrate that obesity and T2D induced by introgression of the Koletsky leptin receptor mutation in the BBDR rat result in islet expansion associated with protection from T1D in female but not male BBDR. <sup>lepr-/lepr-,Gimap5-/Gimap5-</sup> congenic rats. BBDR. <sup>lepr-/lepr-,Gimap5-/Gimap5-</sup> congenic rats should prove valuable to study interactions between lack of leptin receptor signaling, obesity, and sex-specific T2D and T1D.</p>},
  author       = {Moralejo, Daniel H. and Hansen, Carl T. and Treuting, Piper and Hessner, Martin J and Fuller, Jessica M. and Van Yserloo, Brian and Jensen, Richard and Osborne, William and Kwitek, Anne E. and Lernmark, Åke},
  issn         = {1094-8341},
  keyword      = {Diabetes,Islet inflammation,Lymphopenia,Obesity},
  language     = {eng},
  number       = {1},
  pages        = {9--20},
  publisher    = {American Physiological Society},
  series       = {Physiological Genomics},
  title        = {Differential effects of leptin receptor mutation on male and female BBDR.Gimap5-/Gimap5- spontaneously diabetic rats},
  url          = {http://dx.doi.org/10.1152/physiolgenomics.00186.2009},
  volume       = {41},
  year         = {2010},
}