Nature | Vol 577 | 16 January 2020 | 411
chenodeoxycholic/ursodeoxycholic acids or cholic/chenodeoxycholic/
ursodeoxycholic acids) restored colonic frequencies of both RORγ+ Treg
cells and FOXP3+ Treg cells close to that in rich-diet mice (Fig. 1e and
Extended Data Fig. 2a, b). Similarly, a mixture of eight representative
secondary BAs from bacterial oxidation and dehydroxylation path-
ways significantly increased the number of colonic RORγ+ Treg cells
and FOXP3+ Treg cells in minimal-diet mice (Fig. 1e and Extended Data
Fig. 2a, b). We tested several more combinations of secondary BAs and
found that only a combination of lithocholic/3-oxo-lithocholic acids
restored colonic RORγ+ Treg counts (Fig. 1e). No similar effect of these
BAs was found on colonic type 17 T helper (TH17) cells (Extended Data
Fig. 2c), or on RORγ+ Treg cells or TH17 cells from the spleen, mesenteric
lymph node or small intestine (Extended Data Fig. 2d, e). These results
indicated that certain primary and secondary BA species within a BA
pool preferentially regulate RORγ+ Treg cells and that modulation of this
Treg cell population by BAs is both cell-type and tissue-type specific.
FOXP3
+
(% of TCR
+β
CD4
+)
Helios-FITC
ROR
γ-PE
Helios-FITC
ROR
γ-PE
9.6%
GF-
rich diet
SPF-
minimal diet
21.7%
SPF-
rich diet
46.8%
a b
e
0
10
20
30
40
60
50
ROR
+γ
Helios
- T
reg
(% of FOXP3
+)
***
***
cd
***
***
** ***
***
***
***
**
***
Minimal diet
Rich diet +
- +++++ ++ ++++ +++++++ + +
––––––
+
––
+
–––––
+
––––––
+
–––––
ROR
+γ
Helios
- T
reg
(% of FOXP3
+)
SPF-
minimal diet
CA/CDCA/UDCA
38.0%
SPF-
minimal diet
CA alone
20.1%
SPF-
minimal diet
CDCA alone
19.6%
SPF-
minimal diet
UDCA alone
21.2%
SPF-
minimal diet
Oxo-BAs/
LCA/DCA
35.2%
SPF-
minimal diet
21.0%
2 mM CA 2 mM LCA
2 mM LCA/DCA mix1 mM oxo-BAs mix
2 mM oxo-CAs/DCA mix2 mM 3-oxo-LCA/LCA mix
1 mM oxo-BAs/LCA/DCA mix
2 mM DCA
2 mM 3-oxo-LCA2 mM 3-oxo-CA2 mM 7-oxo-CA
2 mM 7-oxo-CDCA2 mM 12-oxo-DCA2 mM 12-oxo-CA
2 mM CA/CDCA/UDCA mi
x
3 mM CA/CDCA mix3 mM CA/UDCA mix
3 mM CDCA/UDCA mix
2 mM CDCA2 mM UDC
A
6 mM CA
6 mM CDCA6 mM UDCA
Primary BAs Secondary BAs
0
10
20
30
40
50
60
0
10
20
30
40
50
60
SPF-rich diet SPF-minimal diet
GF-rich diet
(n = 7) (n = 7)
(n = 7)
GF-rich diet
SPF-rich diet
(n = 5)
(n = 6)
(n = 5)
SPF-minimal diet
n = 7n = 6n = 4n = 8n = 8n = 6n = 6n = 6n = 5n = 6n = 6n = 10n = 8n = 7n = 6n = 6n = 6n = 7n = 8n = 6n = 8n = 6n = 6n = 6n = 9
GF-rich diet
SPF-rich diet
(n = 5)
(n = 6)
(n = 5)
SPF-minimal diet
GF-rich diet
SPF-rich diet
(n = 5)
(n = 6)
(n = 5)
SPF-minimal diet
CA
CDCAUDCAαMCA βMCA
Deconjugated primary bile acids
(μg per g faeces)
***
** *
**
*
**
(^100) ** ***
20
30
30
90
150
210
210
510
1,110 810
1,410
DC
A
LCA
3-oxo-CA3-oxo-LCA7-oxo-CA
7-oxo-CDCA12-oxo-CA12-oxo-DCA
ωMCA
Secondary bile acids
(μg per g faeces)
0
25
50
75
100
350
850
1,350
1,850
2,350
TC
A
TCDCATUDCATα
MCA
Tβ
MCA
Conjugated primary bile acids
(μ
g per g faeces)
3
6
9
12
0
15
(^13030)
230
330430
530
Fig. 1 | Gut BA metabolites are essential for colonic RORγ+ Treg cell
maintenance. a, Beginning at 3 weeks of age, three groups of mice were fed
special diets for 4 weeks. SPF mice were fed either a nutrient-rich or a minimal
diet, and GF mice were fed the nutrient-rich diet. Representative plots and
frequencies of RORγ+Helios− in the FOXP3+CD4+TCRβ+ Treg cell population are
shown. b–d, Liquid chromatography–mass spectrometry (LC–MS)
quantification of faecal conjugated primary BAs (b), deconjugated primary
BAs (c) and secondary BAs (d) from groups of mice fed as in a. The BAs
determined were cholic acid (CA), chenodeoxycholic acid (CDCA),
ursodeoxycholic acid (UDCA), α-muricholic acid (αMCA), βMCA, deoxycholic
acid (DCA), lithocholic acid (LCA), 3-oxo-CA, 3-oxo-LCA, 7-oxo-CA, 7-oxo-
CDCA, 12-oxo-CA, 12-oxo-DCA, ωMCA and taurine-conjugated species (TCA,
TCDCA, TUDCA, TαMCA and TβMCA). e, Three-week-old SPF mice were fed a
nutrient-rich diet, a minimal diet, or a minimal diet supplemented with one or
more primary or secondary BAs in drinking water for 4 weeks. Representative
plots and frequencies of colonic RORγ+Helios− in the FOXP3+CD4+TCRβ+ Treg cell
population and of colonic FOXP3+ in the CD4+TCRβ+ cell population are shown.
The BAs used in the feed were CA, CDCA, UDCA, DCA, LCA, 3-oxo-CA, 3-oxo-
LCA, 7-oxo-CA, 7-oxo-CDCA, 12-oxo-CA, 12-oxo-DCA and various indicated BA
combinations. Data are representative of at least two independent
experiments in a–d. Data are pooled from three independent experiments in e.
n represents biologically independent animals. Data are mean ± s.e.m.
P < 0.05, P < 0.01, P < 0.001, one-way analysis of variance (ANOVA) followed
by the Bonferroni post hoc test.