2015
DOI: 10.1371/journal.pone.0144480
|View full text |Cite
|
Sign up to set email alerts
|

Correction: Petasites japonicus Stimulates the Proliferation of Mouse Spermatogonial Stem Cells

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
3
0

Year Published

2017
2017
2020
2020

Publication Types

Select...
4

Relationship

1
3

Authors

Journals

citations
Cited by 4 publications
(3 citation statements)
references
References 1 publication
0
3
0
Order By: Relevance
“…The levels of LH, FSH, testosterone, cholesterol, glycogen, and sialic acid came back to normal, which supported the fertility enhancing activities. Petasites japonicus MeOH extract proliferated the generation and activity of spermatogonial stem cells when treated to SSC/C57BL/6 mice at doses of 0.1, 1, 10 µg/mL for 7 days [71]. Elevated levels of LHX1 and GFRα1 were observed, which were used as markers of differentiation of spermatogonia at the basement membrane of seminiferous tubules.…”
Section: In Vivo Studiesmentioning
confidence: 99%
“…The levels of LH, FSH, testosterone, cholesterol, glycogen, and sialic acid came back to normal, which supported the fertility enhancing activities. Petasites japonicus MeOH extract proliferated the generation and activity of spermatogonial stem cells when treated to SSC/C57BL/6 mice at doses of 0.1, 1, 10 µg/mL for 7 days [71]. Elevated levels of LHX1 and GFRα1 were observed, which were used as markers of differentiation of spermatogonia at the basement membrane of seminiferous tubules.…”
Section: In Vivo Studiesmentioning
confidence: 99%
“…The equation is calculated on the assumption that the number of germ cells was increased than initial number in control. Actually, the number of germ cells enriched for SSCs was increased 1.98-fold (2 × 10 5 to 3.8 × 10 5 ) on the average 59 .…”
Section: Methodsmentioning
confidence: 99%
“…After purification, Thy-1-positive (Thy-1 + ) cells were placed on 12-well culture plates containing mitotically inactivated SIM mouse embryo-derived thioguanine- and ouabain-resistant (STO) feeder cells. The cells were cultured in mouse serum-free medium (mSFM) including 10 ng/mL glial cell line-derived neurotrophic factors (GDNF; R&D Systems, Minneapolis, MN, USA), 75 ng/mL GDNF family receptor α1 (GFRα1; R&D Systems), and 1 ng/mL basic fibroblast growth factor 2 (bFGF2; BD Biosciences) as previously reported 57 59 . The culture medium was replaced every 2–3 days, and the cultured cells were passaged in a 1:2 or 1:3 ratio every week.…”
Section: Methodsmentioning
confidence: 99%