Literature DB >> 17714088

Role of macrophages in complications of type 2 diabetes.

G H Tesch1.   

Abstract

1. Macrophage accumulation is a feature of Type 2 diabetes and is associated with the development of diabetic complications (nephropathy, atherosclerosis, neuropathy and retinopathy). The present article reviews the current evidence that macrophages contribute to the complications of Type 2 diabetes. 2. Macrophage-depletion studies in rodent models have demonstrated a causal role for macrophages in the development of diabetic complications. 3. Components of the diabetic milieu (high glucose, advanced glycation end-products and oxidized low-density lipoprotein) promote macrophage accumulation (via induction of chemokines and adhesion molecules) and macrophage activation within diabetic tissues. 4. Macrophages mediate diabetic injury through a variety of mechanisms, including production of reactive oxygen species, cytokines and proteases, which result in tissue damage leading to sclerosis. 5. A number of existing and experimental therapies can indirectly reduce macrophage-mediated injury in diabetic complications. The present article discusses the use of these therapies, given alone and in combination, in suppressing macrophage accumulation and activity. 6. In conclusion, current evidence supports a critical role for macrophages in the evolution of diabetic complications. Present therapies are limited in slowing the progression of macrophage-mediated injury. Novel strategies that are more specific at targeting macrophages may provide better protection against the development of Type 2 diabetic complications.

Entities:  

Mesh:

Year:  2007        PMID: 17714088     DOI: 10.1111/j.1440-1681.2007.04729.x

Source DB:  PubMed          Journal:  Clin Exp Pharmacol Physiol        ISSN: 0305-1870            Impact factor:   2.557


  60 in total

1.  Ursolic acid protects diabetic mice against monocyte dysfunction and accelerated atherosclerosis.

Authors:  Sarah L Ullevig; Qingwei Zhao; Debora Zamora; Reto Asmis
Journal:  Atherosclerosis       Date:  2011-06-17       Impact factor: 5.162

2.  Monocyte/macrophage chemokine receptor CCR2 mediates diabetic renal injury.

Authors:  Alaa S Awad; Gilbert R Kinsey; Konstantine Khutsishvili; Ting Gao; W Kline Bolton; Mark D Okusa
Journal:  Am J Physiol Renal Physiol       Date:  2011-08-31

3.  Macrophages directly mediate diabetic renal injury.

Authors:  Hanning You; Ting Gao; Timothy K Cooper; W Brian Reeves; Alaa S Awad
Journal:  Am J Physiol Renal Physiol       Date:  2013-10-30

Review 4.  Transcriptional control of macrophage polarisation in type 2 diabetes.

Authors:  Karima Drareni; Jean-François Gautier; Nicolas Venteclef; Fawaz Alzaid
Journal:  Semin Immunopathol       Date:  2019-05-02       Impact factor: 9.623

Review 5.  Diabetic neuropathy: clinical manifestations and current treatments.

Authors:  Brian C Callaghan; Hsinlin T Cheng; Catherine L Stables; Andrea L Smith; Eva L Feldman
Journal:  Lancet Neurol       Date:  2012-05-16       Impact factor: 44.182

6.  Folate receptor expression on murine and human adipose tissue macrophages.

Authors:  Michael J Hansen; N Achini Bandara; Philip S Low
Journal:  Inflamm Res       Date:  2015-07-07       Impact factor: 4.575

7.  Lymphocytes promote albuminuria, but not renal dysfunction or histological damage in a mouse model of diabetic renal injury.

Authors:  A K H Lim; F Y Ma; D J Nikolic-Paterson; A R Kitching; M C Thomas; G H Tesch
Journal:  Diabetologia       Date:  2010-04-27       Impact factor: 10.122

8.  Protective role of small pigment epithelium-derived factor (PEDF) peptide in diabetic renal injury.

Authors:  Alaa S Awad; Ting Gao; Anzor Gvritishvili; Hanning You; Yanling Liu; Timothy K Cooper; W Brian Reeves; Joyce Tombran-Tink
Journal:  Am J Physiol Renal Physiol       Date:  2013-07-24

Review 9.  Role of the Immune System in Diabetic Kidney Disease.

Authors:  Fionnuala B Hickey; Finian Martin
Journal:  Curr Diab Rep       Date:  2018-03-12       Impact factor: 4.810

Review 10.  Mechanisms of disease: the oxidative stress theory of diabetic neuropathy.

Authors:  Claudia Figueroa-Romero; Mahdieh Sadidi; Eva L Feldman
Journal:  Rev Endocr Metab Disord       Date:  2008-12       Impact factor: 6.514

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.