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. 2018 Dec 14;9:763. doi: 10.3389/fendo.2018.00763

Table 1.

Outcome of manipulation of FSH action and defects on testis mass, number of Sertoli cells, and completion of spermatogenesis.

Treatment/mouse model/human condition Species Testis mass or volume (%)* Number of Sertoli cells (%)* Number of round (r) or elongated (e) spermatids (%) or sperm count (s)* Ratio of round spermatids to number of Sertoli cells (%)* Reference(s)
Fshb knockout Mouse 40 57–70 40(r), 37(e) 57 (24, 25)
Fshr knockout Mouse 42 55** 36(r)** 69**,*** (26)
FSHR null mutation 566CT; A189V Human 27–100 n/a oligospermic-normospermic (s) n/a (27)
FSHB missense, frameshift and truncating mutations Human 7–80 n/a or reduced number of Sertoli cells azoospermic (s) n/a (28) and references therein
Acvr2a knockout (stimulation of FSH prevented) Mouse 40–43 60–61 45(r), 41(e) 75 (24)
hpg (gonadotropin-deficient hypogonadal) + tgFSH expression Mouse 500 162** Increased, but low (r), hardly detectable (e) Cannot be measured due to the absence of spermatids in hpg mice (29)
(hpg + T implant) + tgFSH expression Mouse 166 132** 161(r), 184(e)** 117** (29)
Neonatal treatment with rhFSH Rat 124 149 n/a n/a (30)
Fshr-CAMG1738C; D580HtgFSHR expression Mouse 94 85 87(r), 87(e) 103 (31)
LuRKO; Lhcgr knockout Mouse 19 29 4.8(r), 0(e) 16 (31)
Fshr-CAM/LuRKO crossbreed Mouse 86 83 94(r), 51(e) 115 (31)
*

In comparison to corresponding controls in each experiment.

**

Estimated from the charts presented in the article.

***

All germ cells/Sertoli cells; n/a, data not available; rh, recombinant human; tg, transgenic; CAM, constitutively activating mutation.