Immunocytochemical Identification of Mammalian Differentiating Neurons in the Process of Adult Neurogenesis in the Hippocampal Dentate Gyrus

Author(s):  
Oliver von Bohlen und Halbach
2010 ◽  
Vol 35 (11) ◽  
pp. 1725-1732 ◽  
Author(s):  
Seungjoo Lee ◽  
Dong Hyun Kim ◽  
Dong Hwa Lee ◽  
Su Jin Jeon ◽  
Chang Hwan Lee ◽  
...  

Molecules ◽  
2018 ◽  
Vol 23 (9) ◽  
pp. 2178 ◽  
Author(s):  
Fei Huang ◽  
Yunyi Lan ◽  
Liyue Qin ◽  
Huaihuai Dong ◽  
Hailian Shi ◽  
...  

Astragaloside IV (ASI) has been reported to promote neural stem cells proliferation in vitro and CXCR2 expression on neutrophils. The present study was aimed to investigate the influence of ASI on adult neurogenesis in hippocampal dentate gyrus (DGs) of mouse and to discuss the possible underlying mechanisms. Total number of proliferative cells (BrdU+), pre-mature neurons (DCX+), early proliferative cells (BrdU+/DCX+), proliferative radial gila-like cells (BrdU+/GFAP+) and newly generated neurons (BrdU+/NeuN+) after ASI or vehicle administration for two weeks were counted, respectively. The results showed that BrdU+ cells and DCX+ cells were significantly increased in DGs of mice administered with ASI. The numbers of BrdU+/DCX+, BrdU+/GFAP+ cells and BrdU+/NeuN+ cells were also elevated in the ASI group. Correspondingly, ASI increased the protein expression of hippocampal DCX, GFAP and NeuN. Further study disclosed that ASI remarkably up-regulated the mRNA and protein expressions of CXCL1 as well as that of CXCR2 in the hippocampus. The promotive effect of ASI on DCX, GFAP and NeuN protein expression was abolished by SB225002, the inhibitor of CXCR2. Our results indicated that ASI modulated the homeostasis of the CXCL1/CXCR2 signaling pathway, which might be responsible for the increased neurogenesis within the hippocampal DGs of mice.


2017 ◽  
Vol 661 ◽  
pp. 121-125 ◽  
Author(s):  
Kaori Yagishita ◽  
Ritsuko Suzuki ◽  
Shota Mizuno ◽  
Ritsuko Katoh-Semba ◽  
Tetsushi Sadakata ◽  
...  

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Zheng Yu ◽  
Dong Lin ◽  
Yanzi Zhong ◽  
Bin Luo ◽  
Shengsheng Liu ◽  
...  

2017 ◽  
pp. 389-408
Author(s):  
Arjen van Ooyen ◽  
Gertraud Teuchert-Noodt ◽  
Keren Grafen ◽  
Markus Butz-Ostendorf

2011 ◽  
Vol 488 (1) ◽  
pp. 70-75 ◽  
Author(s):  
Congmin Wang ◽  
Mingguang Zhang ◽  
Chifei Sun ◽  
Yuqun Cai ◽  
Yan You ◽  
...  

2015 ◽  
Vol 16 (3) ◽  
pp. 245 ◽  
Author(s):  
Sung Min Nam ◽  
Jong Whi Kim ◽  
Dae Young Yoo ◽  
Jung Hoon Choi ◽  
Woosuk Kim ◽  
...  

2017 ◽  
pp. 441-448 ◽  
Author(s):  
A. PISTIKOVA ◽  
H. BROZKA ◽  
A. STUCHLIK

The function of adult neurogenesis in the dentate gyrus is not yet completely understood, though many competing theories have attempted to explain the function of these newly-generated neurons. Most theories give adult neurogenesis a role in aiding known hippocampal/dentate gyrus functions. Other theories offer a novel role for these new cells based on their unique physiological qualities, such as their low excitability threshold. Many behavioral tests have been used to test these theories, but results have been inconsistent and often contradictory. Substantial variability in tests and protocols may be at least partially responsible for the mixed results. On the other hand, conflicting results arising from the same tests can serve as aids in elucidating the function of adult neurogenesis. Here, we offer a hypothesis that considers the cognitive nature of tasks commonly used to assess the function of adult neurogenesis, and introduce a dichotomy between tasks focused on discrimination vs. generalization. We view these two aspects as opposite ends of the continuous spectrum onto which traditional tests can be mapped. We propose that high neurogenesis favors behavioral discrimination while low adult neurogenesis favors behavioral generalization of a knowledge or rule. Since many tasks require both, the effects of neurogenesis could be cancelled out in many cases. Although speculative, we hope that our view presents an interesting and testable hypothesis of the effect of adult neurogenesis in traditional behavioral tasks. We conclude that new, carefully designed behavioral tests may be necessary to reach a final consensus on the role of adult neurogenesis in behavior.


2001 ◽  
Vol 12 (1) ◽  
pp. 8-14
Author(s):  
Gertraud Teuchert-Noodt ◽  
Ralf R. Dawirs

Abstract: Neuroplasticity research in connection with mental disorders has recently bridged the gap between basic neurobiology and applied neuropsychology. A non-invasive method in the gerbil (Meriones unguiculus) - the restricted versus enriched breading and the systemically applied single methamphetamine dose - offers an experimental approach to investigate psychoses. Acts of intervening affirm an activity dependent malfunctional reorganization in the prefrontal cortex and in the hippocampal dentate gyrus and reveal the dopamine position as being critical for the disruption of interactions between the areas concerned. From the extent of plasticity effects the probability and risk of psycho-cognitive development may be derived. Advance may be expected from insights into regulatory mechanisms of neurogenesis in the hippocampal dentate gyrus which is obviously to meet the necessary requirements to promote psycho-cognitive functions/malfunctions via the limbo-prefrontal circuit.


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