Guangjin Pan

Dr. Guangjin Pan


Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 September 2007 in Cell Stem Cell
Verified
Journal Article
Closed access
GPGuangjin Pan
Guangjin Pan
STShulan Tian
Shulan Tian
JNJeff Nie
Jeff Nie
CYChuhu Yang
Chuhu Yang
VRVictor Ruotti
Victor Ruotti
JTJames A. Thomson
James A. Thomson

9 January 2007 in Cell Research
Verified
Journal Article
Closed access
GPGuangjin Pan
Guangjin Pan
JTJames A Thomson
James A Thomson

24 August 2020 in Nature Metabolism
Verified
Journal Article
Closed access
PDF file
LLLinpeng Li
Linpeng Li
KCKeshi Chen
Keshi Chen
TWTianyu Wang
Tianyu Wang
YWYi Wu
Yi Wu
GXGuangsuo Xing
Guangsuo Xing
Xingguo LiuXingguo Liu
Xingguo Liu

1 December 2002 in Cell Research
Verified
Journal Article
Closed access
GPGuangjin Pan
Guangjin Pan
ZCZeng Yi Chang
Zeng Yi Chang
HSHans R. Schöler
Hans R. Schöler
DPDuanqing Pei
Duanqing Pei

1 January 2013 in Nature Methods
Verified
Journal Article
Open access
PDF file
LWLihui Wang
Lihui Wang
LWLinli Wang
Linli Wang
WHWenhao Huang
Wenhao Huang
HSHuanxing Su
Huanxing Su
YXYanting Xue
Yanting Xue
DPDuanqing Pei
Duanqing Pei
Human neural stem cells hold great promise for research and therapy in neural disease. We describe the generation of integration-free and expandable human neural progenitor cells (NPCs). We combined an episomal system to deliver reprogramming factors with a chemically defined culture medium to reprogram epithelial-like cells from human urine into NPCs (hUiNPCs). These transgene-free hUiNPCs can self-renew and can differentiate into multiple functional neuronal subtypes and glial cells in vitro. Although functional in vivo analysis is still needed, we report that the cells survive and differentiate upon transplant into newborn rat brain.

21 June 2006 in The FASEB Journal
Verified
Journal Article
Open access
PDF file
GPGuangjin Pan
Guangjin Pan
JLJun Li
Jun Li
YZYali Zhou
Yali Zhou
HZHui Zheng
Hui Zheng
DPDuanqing Pei
Duanqing Pei
Embryonic stem (ES) cells possess the ability to renew themselves while maintaining the capacity to differentiate into virtually all cell types of the body. Current evidence suggests that ES cells maintain their pluripotent state by expressing a battery of transcription factors including Oct4 and Nanog. However, little is known about how ES cells maintain the expression of these pluripotent factors in ES cells. Here we present evidence that Oct4, Nanog, and FoxD3 form a negative feedback loop to maintain their expression in pluripotent ES cells. First, Oct4 maintains Nanog activity by directly activating its promoter at sub‐steady‐state concentration but repressing it at or above steady‐state levels. On the other hand, FoxD3 behaves as a positive activator of Nanog to counter the repressive effect of Oct4. The expression of Oct4 is activated by FoxD3 and Nanog but repressed by Oct4 itself, thus, exerting an important negative feedback loop to limit its own activity. Indeed, overexpression of either FoxD3 or Nanog in ES cells failed to increase the concentration of Oct4 beyond the steady‐state concentration, whereas knocking down either FoxD3 or Nanog reduces the expression of Oct4 in ES cells. Finally, overexpression of Oct4 or Nanog failed to compensate the loss of Nanog or Oct4, respectively, suggesting that both are required for ES self‐renewal and pluripotency. Our results suggest the FoxD3‐Nanog‐Oct4 loop anchors an interdependent network of transcription factors that regulate stem cell pluripotency.—Pan, G., Li, J., Zhou, Y., Zheng, H., Pei, D. A negative feedback loop of transcription factors that controls stem cell pluripotency and self‐renewal. FASEB J. 20, E1094–E1102 (2006)