TSPAN8 Expression Distinguishes Spermatogonial Stem Cells in the Prepubertal Mouse Testis

被引:32
作者
Mutoji, Kazadi [1 ]
Singh, Anukriti [1 ]
Thu Nguyen [1 ]
Gildersleeve, Heidi [1 ,2 ]
Kaucher, Amy V. [5 ]
Oatley, Melissa J. [5 ]
Oatley, Jon M. [5 ]
Velte, Ellen K. [3 ,4 ]
Geyer, Christopher B. [3 ,4 ]
Cheng, Keren [1 ]
McCarrey, John R. [1 ]
Hermann, Brian P. [1 ,2 ]
机构
[1] Univ Texas San Antonio, Dept Biol, One UTSA Circle, San Antonio, TX 78249 USA
[2] Univ Texas San Antonio, Genom Core Facil, One UTSA Circle, San Antonio, TX 78249 USA
[3] East Carolina Univ, Dept Anat & Cell Biol, Greenville, NC USA
[4] East Carolina Univ, East Carolina Diabet & Obes Inst, Brody Sch Med, Greenville, NC USA
[5] Washington State Univ, Coll Vet Med, Sch Mol Biosci, Ctr Reprod Biol, Pullman, WA 99164 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
epigenetics; single-cell; spermatogonial stem cells; surface marker; transcriptome; transplantation; BINDING PROTEIN NANOS2; ACID GENE-8 STRA8; RETINOIC ACID; UNDIFFERENTIATED SPERMATOGONIA; SELF-RENEWAL; DIFFERENTIAL GENE; IN-VIVO; SPERMATOGENESIS; GERMLINE; TRANSPLANTATION;
D O I
10.1095/biolreprod.116.144220
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Precise separation of spermatogonial stem cells (SSCs) from progenitor spermatogonia that lack stem cell activity and are committed to differentiation remains a challenge. To distinguish between these spermatogonial subtypes, we identified genes that exhibited bimodal mRNA levels at the single-cell level among undifferentiated spermatogonia from Postnatal Day 6 mouse testes, including Tspan8, Epha2, and Pvr, each of which encode cell surface proteins useful for cell selection. Transplantation studies provided definitive evidence that a TSPAN8-high subpopulation is enriched for SSCs. RNA-seq analyses identified genes differentially expressed between TSPAN8-high and -low subpopulations that clustered into multiple biological pathways potentially involved in SSC renewal or differentiation, respectively. Methyl-seq analysis identified hypomethylated domains in the promoters of these genes in both subpopulations that colocalized with peaks of histone modifications defined by ChIP-seq analysis. Taken together, these results demonstrate functional heterogeneity among mouse undifferentiated spermatogonia and point to key biological characteristics that distinguish SSCs from progenitor spermatogonia.
引用
收藏
页码:1 / 14
页数:14
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