The DOI matches its Crossref record.
Mouse primordial germ cells produce cysts that partially fragment prior to meiosis
Open accessAbstract
Mammalian germ cells divide mitotically and form nests of associated cells just prior to entering meiosis. At least some nests contain germline cysts that arise by synchronous, incomplete mitotic divisions, but others may form by aggregation. To systematically investigate early murine germ cell development, we lineage marked the progeny of individual, newly arrived primordial germ cells in the E10.5 gonad. All the marked germ cells initially develop into clones containing two, four or eight cells, indicating cyst formation. Surprisingly, growing cysts in both sexes partially fragment into smaller cysts prior to completion and associate with cysts from unrelated progenitors. At the time divisions cease, female clones comprise five cysts on average that eventually give rise to about six primordial follicles. Male cyst cells break apart and probably become spermatogonial stem cells. Thus, cysts are invariant units of mouse germ cell development and cyst fragmentation provides insight into the amplification of spermatogonial stem cells and the origin of primordial follicles.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cited by
Mouse oocytes differentiate through organelle enrichment from sister cyst germ cells
Lei, L., & Spradling, A. C. (2016) · Science · doi:10.1126/science.aad2156 · Cited by 313
Self-citationNiu, W., & Spradling, A. C. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2005570117 · Cited by 267
Self-citationA role for retrotransposon LINE-1 in fetal oocyte attrition in mice
Malki, S., van der Heijden, G. W., O’Donnell, K. A., Martin, S. L., & Bortvin, A. (2014) · Developmental Cell · doi:10.1016/j.devcel.2014.04.027 · Cited by 215
PI3K/PTEN/Akt and TSC/mTOR signaling pathways, ovarian dysfunction, and infertility: an update
Makker, A., Goel, M. M., & Mahdi, A. A. (2014) · Journal of Molecular Endocrinology · doi:10.1530/jme-14-0220 · Cited by 214
Metadata
- Authors
- Lei, L., & Spradling, A. C.
- Venue
- Development
- Publisher
- The Company of Biologists
- Published
- 2013-05-15
- Volume
- 140
- Issue
- 10
- Pages
- 2075-2081
- ISSN
- 0950-1991 (ISSN-L)
- 1477-9129
- OpenAlex
- W2071040218
- Cited by
- 206
- References
- 0
- FWCI
- 12.73
- Type
- journal article
- Language
- en
- Open access
- green
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.