Leptin signaling and leptin resistance

被引:325
作者
Zhou, Yingjiang [1 ]
Rui, Liangyou [2 ]
机构
[1] Pfizer Worldwide Res & Dev, Cambridge Labs, Cambridge, MA 02139 USA
[2] Univ Michigan, Dept Mol & Integrat Physiol, Sch Med, Ann Arbor, MI 48109 USA
关键词
leptin signaling; leptin receptor; energy balance; leptin resistance; obesity;
D O I
10.1007/s11684-013-0263-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Leptin is secreted into the bloodstream by adipocytes and is required for the maintenance of energy homeostasis and body weight. Leptin deficiency or genetic defects in the components of the leptin signaling pathways cause obesity. Leptin controls energy balance and body weight mainly through leptin receptor b (LEPRb)-expressing neurons in the brain, particularly in the hypothalamus. These LEPRb-expressing neurons function as the first-order neurons that project to the second-order neurons located within and outside the hypothalamus, forming a neural network that controls the energy homeostasis and body weight. Multiple factors, including inflammation and endoplasmic reticulum (ER) stress, contribute to leptin resistance. Leptin resistance is the key risk factor for obesity. This review is focused on recent advance about leptin action, leptin signaling, and leptin resistance.
引用
收藏
页码:207 / 222
页数:16
相关论文
共 196 条
[1]
Role of leptin in the neuroendocrine response to fasting [J].
Ahima, RS ;
Prabakaran, D ;
Mantzoros, C ;
Qu, DQ ;
Lowell, B ;
MaratosFlier, E ;
Flier, JS .
NATURE, 1996, 382 (6588) :250-252
[2]
AGRP neurons are sufficient to orchestrate feeding behavior rapidly and without training [J].
Aponte, Yexica ;
Atasoy, Deniz ;
Sternson, Scott M. .
NATURE NEUROSCIENCE, 2011, 14 (03) :351-355
[3]
Divergence of melanocortin pathways in the control of food intake and energy expenditure [J].
Balthasar, N ;
Dalgaard, LT ;
Lee, CE ;
Yu, J ;
Funahashi, H ;
Williams, T ;
Ferreira, M ;
Tang, V ;
McGovern, RA ;
Kenny, CD ;
Christiansen, LM ;
Edelstein, E ;
Choi, B ;
Boss, O ;
Aschkenasi, C ;
Zhang, CY ;
Mountjoy, K ;
Kishi, T ;
Elmquist, JK ;
Lowell, BB .
CELL, 2005, 123 (03) :493-505
[4]
Leptin receptor signaling in is required for normal body POW neurons weight homeostasis [J].
Balthasar, N ;
Coppari, R ;
McMinn, J ;
Liu, SM ;
Lee, CE ;
Tang, V ;
Kenny, CD ;
McGovern, RA ;
Chua, SC ;
Elmquist, JK ;
Lowell, BB .
NEURON, 2004, 42 (06) :983-991
[5]
Activation of downstream signals by the long form of the leptin receptor [J].
Banks, AS ;
Davis, SM ;
Bates, SH ;
Myers, MG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (19) :14563-14572
[6]
Impaired transport of leptin across the blood-brain barrier in obesity is acquired and reversible [J].
Banks, WA ;
Farrell, CL .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2003, 285 (01) :E10-E15
[7]
Leptin enters the brain by a saturable system independent of insulin [J].
Banks, WA ;
Kastin, AJ ;
Huang, WT ;
Jaspan, JB ;
Maness, LM .
PEPTIDES, 1996, 17 (02) :305-311
[8]
Impaired transport of leptin across the blood-brain barrier in obesity [J].
Banks, WA ;
DiPalma, CR ;
Farrell, CL .
PEPTIDES, 1999, 20 (11) :1341-1345
[9]
PTP1B and SHP2 in POMC neurons reciprocally regulate energy balance in mice [J].
Banno, Ryoichi ;
Zimmer, Derek ;
De Jonghe, Bart C. ;
Atienza, Marybiess ;
Rak, Kimberly ;
Yang, Wentian ;
Bence, Kendra K. .
JOURNAL OF CLINICAL INVESTIGATION, 2010, 120 (03) :720-734
[10]
STAT3 signalling is required for leptin regulation of energy balance but not reproduction [J].
Bates, SH ;
Stearns, WH ;
Dundon, TA ;
Schubert, M ;
Tso, AWK ;
Wang, YP ;
Banks, AS ;
Lavery, HJ ;
Haq, AK ;
Maratos-Flier, E ;
Neel, BG ;
Schwartz, MW ;
Myers, MG .
NATURE, 2003, 421 (6925) :856-859